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Indazoles as hematopoietic progenitor kinase 1 (HPK1) inhibitors and methods using same

11649255 · 2023-05-16

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Abstract

The present disclosure provides a compound of Formula (I) or pharmaceutically acceptable salts thereof, a composition comprising the compound, methods of using the compound for the treatment of various disorders associated with HPK1, and methods of preparing these compounds. ##STR00001##

Claims

1. A compound of Formula (I): ##STR00703## or a pharmaceutically acceptable salt, hydrate, or solvate, thereof, wherein: X is O or S; L is a bond, —O—, —S—, or —NR.sup.6—; R.sup.1 is alkyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl, wherein R.sup.1 is optionally substituted with one or more substituents independently selected from R.sup.7; R.sup.6 is —H or C.sub.1-6 alkyl; R.sup.7 is C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, oxo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13; R.sup.9 is —H, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl; Each R.sup.10 and R.sup.11 is independently —H, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl, or R.sup.10 and R.sup.11 are taken together with the nitrogen atom to which they are attached to form a 4- to 12-membered heterocyclyl optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; Each R.sup.12 and R.sup.13 is independently C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.3-8 cycloalkyl, aryl, heteroaryl, heterocyclyl, or R.sup.12 and R.sup.13 are taken together with the phosphorus atom to which they are attached to form a 4- to 8-membered heterocyclyl optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; Het is selected from the group consisting of: ##STR00704## Each of R.sup.a, R.sup.b and R.sup.c is independently —H, -D, halo, CF.sub.3, CF.sub.2H, CH.sub.2F, CN, OR.sup.9 or NR.sup.10R.sup.11; R.sup.2 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, hydroxyl, —CD.sub.2OH, —CN, —NO.sub.2, haloalkyl, trimethylsilylethoxymethyl, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13, wherein the C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10c(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; R.sup.3 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —CH.sub.2OH, —CD.sub.2OH, —OH, —CN, —NO.sub.2, haloalkyl, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13; M is a bond, —O—, —S—, or —NR.sup.6—; R.sup.6 is —H or C.sub.1-6 alkyl; R.sup.4 is —H, -D, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, — —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13, wherein C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —CD.sub.3, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —NR.sup.10S(O).sub.2R.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; and R.sup.5 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, hydroxyl, —CH.sub.2OH, —CD.sub.2OH, —CN or haloalkyl.

2. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein L is a bond, and R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, and —N(R.sup.6)C(O)NR.sup.10R.sup.11.

3. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein each of R.sup.2 and R.sup.3 is independently —H, halo, alkylthio, haloalkyl, or alkyl.

4. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein M is a bond, —O—, or —NR.sup.6—; and R.sup.4 is —H, -D, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)NR.sup.10R.sup.11, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, or —S(O).sub.2NR.sup.10R.sup.11, wherein the C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxy, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —CD.sub.3, —NR.sup.10R.sup.11, —NR.sup.10S(O).sub.2R.sup.9, and —NR.sup.10C(═O)R.sup.9.

5. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is a compound of Formula (V): ##STR00705##

6. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein L is a bond, and R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, and —N(R.sup.6)C(O)NR.sup.10R.sup.11.

7. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl.

8. The compound of claim 5 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-2-fluoro-N-(6-(5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-methoxy-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-amino-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-amino-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-bromo-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(methylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(dimethylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-bromo-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-cyano-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(hydroxymethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-ethyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(6-fluoro-5-vinyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1S,2S)-2-fluoro-N-(6-(5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-bromo-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-acetyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-amino-6-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-cyclopropyl-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-cyclopropyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(6-fluoro-5-isopropyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-ethyl-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(5-(difluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; N-(6-(6-fluoro-5-(hydroxymethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; N-(6-(6-fluoro-5-methoxy-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1S,2S)-N-(6-(5-(difluoromethyl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-bromo-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-(difluoromethyl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1S,2S)-N-(6-(5,7-dichloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7-dimethyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(dimethylphosphoryl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-chloro-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-bromo-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(6,7-difluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(5-methyl-7-vinyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylsulfonyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-bromo-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylsulfonyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-7-methoxy-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-methoxy-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-acrylamido-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-ethoxy-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-acrylamido-5-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(4-methylpiperazin-1-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 2-(hydroxymethyl)-N-(6-(5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-morpholino-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(ethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(diethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(pyrrolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(azetidin-1-yl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(6-amino-5-chloro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(7-methoxy-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(6-acrylamido-5-chloro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(6-acrylamido-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((2-hydroxyethyl)thio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(dimethylamino)-5-ethyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-7-(2-hydroxyethyl)thio)-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-ethyl-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-ethyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-hydroxy-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7-bis(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-ethyl-6,7-difluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylsulfinyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-acetamido-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylsulfonyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylsulfinyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(6,7-difluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; methyl 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-5-methyl-1H-indazole-7-carboxylate; (1S,2S)-N-(6-(5-chloro-7-(ethyl(methyl)amino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-acetamido-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; tert-butyl 2-(5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1H-indazol-7-yl)-1-methylhydrazine-1-carboxylate; (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(N-methylacetamido)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; 2-((6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-5-methyl-1 H-indazol-7-yl)thio)ethyl methylcarbamate; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-5-methyl-1 H-indazole-7-carboxylic acid; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazole-7-carboxylic acid; methyl 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazole-7-carboxylate; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(N-methylacetamido)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-methylhydrazineyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-5-ethyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-acetyl-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-acetyl-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6,7-difluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(5-ethyl-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; (1 S,2S)-N-(6-(5-ethoxy-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N,5-trimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(difluoromethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2R)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-oxopyrrolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-2-yl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,5-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(5-ethyl-6-fluoro-7-(trifluoromethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(7-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; 5-chloro-N-ethyl-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-7-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(difluoromethyl)-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyrimidin-2-yl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N-methyl-N-(2,2,2-trifluoroethyl)-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyrimidin-4-yl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-3-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-tetrazol-5-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-cyano-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(dimethylamino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-4-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N-dimethyl-1 H-indazole-5-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-ethoxy-6,7-difluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(3-methyl-2-oxoimidazolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(isopropyl(methyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyclopropyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(hydroxymethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(fluoromethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(3-methyl-1,2,4-oxadiazol-5-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1 H-pyrrol-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((cyanomethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyclopropylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(N-cyclopropyl-2,2,2-trifluoroacetamido)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(3-hydroxypropanamido)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(sec-butylamino)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1-cyanoethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-hydroxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methoxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-fluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1 H-pyrrol-3-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-pyrrol-3-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-pyrrol-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-pyrazol-5-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7((2H-tetrazol-2-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(azetidin-1-ylmethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(pyrrolidin-1-ylmethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(piperidin-1-ylmethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((2H-1,2,3-triazol-2-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((1 H-1,2,3-triazol-1-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((1 H-1,2,4-triazol-1-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((1-methyl-1 H-imidazol-2-yl)thio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 1-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-3-cyclopropylurea; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-methyl-1 H-pyrrol-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-hydroxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methoxymethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(ethoxymethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((1 H-tetrazol-1-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1-(dimethylamino)-1-oxopropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(1-(dimethylamino)ethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((2-(dimethylamino)-2-oxoethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-aminoethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazol-7-yl)-N,N-dimethyl-1 H-pyrrole-3-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-cyclopropoxy-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylamino)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(8-amino-6-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropoxy-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-cyclopentyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((R)-1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-hydroxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-hydroxycyclopentyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-ethanethioamido-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(N-methylacetamido)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((R)-1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-methoxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((tetrahydrofuran-3-yl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-acetamidoethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(1-ethoxy-2,2,2-trifluoroethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1,2,2,2-tetrafluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1-cyclopropylethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((cyclopropylmethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((R)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((S)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-propionamidoethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1,1-difluoropropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-formamidoethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(oxetan-3-ylamino)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(2,2,2-trifluoroacetamido)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide (1 S,2S)-N-(6-(5-chloro-7-(1-((1-cyanocyclopropyl)amino)ethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazol-7-yl)ethyl)cyclobutanecarboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1H-imidazol-5-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-((4,5-dihydro-1H-imidazol-2-yl)amino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylamino)-1-oxopropan-2-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((methylthio)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(1,3-dimethylureido)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylthio)ethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((methylsulfinyl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((methylsulfonyl)methyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(cyano(formamido)methyl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-((1S,2R)-1,2-dimethoxypropyl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(1-(2,2-difluoroacetamido)ethyl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-methyl-1H-imidazol-5-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylsulfinyl)ethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylsulfonyl)ethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1S,2S)-N-(6-(5-chloro-7-(1-(ethylamino)-1-oxopropan-2-yl)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

9. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-C.sub.3 alkyl, C.sub.1-C.sub.3 hydroxyalkyl and C.sub.1-C.sub.3 haloalkyl; R.sup.2 is —H, alkyl, alkylthio, haloalkyl, or halo; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, monoalkylamino, or dialkylamino; R.sup.5 is —H, alkyl, or halo.

10. The compound of claim 5 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(isopropylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

11. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, monoalkylamino, or dialkylamino; and R.sup.5 is —H, alkyl, or halo.

12. The compound of claim 5 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-bromo-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-methoxy-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-ethoxy-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(ethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-5-ethyl-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-ethyl-6-fluoro-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7-bis(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(6,7-difluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-5-ethyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N,5-trimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2R)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-oxopyrrolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-N-ethyl-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-3-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-4-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(3-methyl-2-oxoimidazolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyclopropyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((cyanomethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1-cyanoethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-hydroxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-fluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methoxymethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(ethoxymethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropoxy-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-hydroxycyclopentyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-acetamidoethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1,2,2,2-tetrafluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((R)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((S)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1,1-difluoropropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-formamidoethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(2,2,2-trifluoroacetamido)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazol-7-yl)ethyl)cyclobutanecarboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylamino)-1-oxopropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((methylthio)methyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylthio)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyano(formamido)methyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(1-(2,2-difluoroacetamido)ethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1 S,2S)-N-(6-(5-chloro-7-(1-(ethylamino)-1-oxopropan-2-yl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

13. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, alkylcarbonyl, dialkylaminocarbonyl, oxopyrrolidinyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, pyridinyl, monoalkylamino, or dialkylamino; and R.sup.5 is —H, alkyl, or halo.

14. The compound of claim 5 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-bromo-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-bromo-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-7-methoxy-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-methoxy-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-ethoxy-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(ethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(diethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2-hydroxyethyl)thio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-5-ethyl-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-ethyl-6-fluoro-7-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7-bis(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-ethyl-6,7-difluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(6,7-difluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-7-(ethyl(methyl)amino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(N-methylacetamido)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-ethoxy-5-ethyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-ethyl-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N,N,5-trimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(6-(7-(ethyl(methyl)amino)-6-fluoro-5-methyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(difluoromethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2R)-N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-oxopyrrolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-ethyl-6-fluoro-7-(trifluoromethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-N-ethyl-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyrimidin-2-yl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-3-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methyl(pyridin-4-ylmethyl)amino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(3-methyl-2-oxoimidazolidin-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyclopropyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(hydroxymethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(fluoromethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1 H-pyrrol-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((cyanomethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyclopropylamino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(sec-butylamino)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1-cyanoethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-hydroxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methoxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-fluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-pyrrol-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-methyl-1 H-pyrazol-5-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7((2H-tetrazol-2-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((2H-1,2,3-triazol-2-yl)methyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-methyl-1 H-pyrrol-1-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(methoxymethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(ethoxymethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-cyclopropoxy-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropoxy-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-isopropyl-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-cyclopentyl-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-hydroxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2-hydroxycyclopentyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-((S)-1-(1 H-tetrazol-1-yl)ethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-methoxyethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(7-(1-acetamidoethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1,2,2,2-tetrafluoroethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((cyclopropylmethyl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((R)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((S)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-propionamidoethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-((1,1-difluoropropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-formamidoethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(2,2,2-trifluoroacetamido)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)imidazo[1,2-a]pyridin-6-yl)-1 H-indazol-7-yl)ethyl)cyclobutanecarboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylamino)-1-oxopropan-2-yl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-((methylthio)methyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(methylthio)ethyl)-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(cyano(formamido)methyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(6-(5-chloro-7-(1-(2,2-difluoroacetamido)ethyl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1 S,2S)-N-(6-(5-chloro-7-(1-(ethylamino)-1-oxopropan-2-yl)-6-fluoro-1 H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

15. The compound of claim 1 or a pharmaceutically acceptable salt thereof, which is a compound of Formula (VI): ##STR00706##

16. A pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and the compound of claim 1 or a pharmaceutically acceptable salt thereof.

17. The compound of claim 15 or a pharmaceutically acceptable salt thereof, wherein L is a bond, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxy alkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkylamidoalkyl, haloalkylcarbonylaminoalkyl, alkylamidoalkyl, hydroxyhaloalkyl, haloalkenyl, cycloalkyl, cyano, cyanoalkyl, dimethylamino, dimethylaminoethyl, methylaminocarbonyl, dimethylaminocarbonyl, methylaminooxoethyl, am inocarbonylalkyl, acetamindoethyl, dialkylaminocycloalkyl, aminocycloalkyl, methylaminocycloalkyl, cycloalkylalkyl, cycloalkyl(hydroxy)alkyl, cycloalkylamidoalkyl, cycloalkylaminocarbonyl, hydroxycycloalkyl, methoxycycloalkyl, cycloalkyl(methoxy)methyl, alkoxycarbonyl, alkylcarbonyl, alkylamidoalkyl, alkoxyalkyl, alkenyl, methylsulfonamidoethyl, imidazolylethyl, dioxanyl, azetidinyl, azetidin ylmethyl, tetrahydrofuranyl, furanyl, pyrimidinyl, pyridinyl, pyrrolyl, halopyrrolidinyl, pyrrolidinyl, methylpyrrolyl, isoxazolyl, tetrazolylalkyl, triazinyl, methylpyrazolyl, or methylpyrazolylmethyl; and R.sup.5 is —H, alkyl, or halo.

18. The compound of claim 15 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-2-fluoro-N-(5-(5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-vinyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(5-methoxy-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-(dimethylamino)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(5-(trifluoromethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-ethyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-acetyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-(dimethylamino)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-bromo-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-cyano-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-cyclopropyl-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-cyclopropyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(5-(hydroxymethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-isopropyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-bromo-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-(difluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methoxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-(difluoromethyl)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(3-chloro-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-3,5-dimethyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-3-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(3-ethynyl-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(3-cyclopropyl-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-3-vinyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(3-ethyl-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5,7-dichloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5,7-dimethyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-7-(dimethylphosphoryl)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(7-chloro-6-fluoro-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(7-bromo-5-chloro-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(6,7-difluoro-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(trifluoromethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(5-methyl-7-vinyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylsulfonyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(7-bromo-6-fluoro-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylsulfonyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-methoxy-5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-methoxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-ethoxy-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(4-methylpiperazin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(diethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-morpholino-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(pyrrolidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(piperazin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(azetidin-1-yl)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((4-(dimethylamino)cyclohexyl)(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((4-hydroxycyclohexyl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl((1R,4R)-4-(methylamino)cyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl((1 S,4S)-4-(methylamino)cyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(7-methoxy-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((tetrahydrofuran-2-yl)methoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((4-(methylamino)cyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-amino-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((4-(dimethylamino)cyclohexyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide dihydrochloride; (1 S,2S)-N-(5-(7-((4-aminocyclohexyl)(methyl)amino)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((4-aminocyclohexyl)amino)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; tert-butyl (4-((5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido) pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazol-7-yl)amino)cyclohexyl)carbamate; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((4-hydroxycyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(diethylamino)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((2-hydroxyethyl)thio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-((2-(methylamino)-2-oxoethyl)thio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide bis(2,2,2-trifluoroacetate); (1 S,2S)-N-(5-(7-((2-(dimethylamino)-2-oxoethyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide bis(2,2,2-trifluoroacetate); (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2-hydroxyethyl)thio)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-7-(ethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 2-((5-ethyl-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1H-indazol-7-yl)thio)acetic acid; (1 S,2S)-N-(5-(7-((3-aminocyclopentyl)(methyl)amino)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-hydroxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5,7-bis(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6,7-difluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylsulfinyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-(2-hydroxyethoxy)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; 2-((6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazol-7-yl)oxy)ethyl carbamate; (1 S,2S)-N-(5-(5-chloro-6,7-difluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-acetamido-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylsulfinyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(2-(1-methylureido)ethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-acetamido-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; tert-butyl 2-(5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido) pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazol-7-yl)-1-methylhydrazine-1-carboxylate; (1 S,2S)-N-(5-(7-ethoxy-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(2-ureidoethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(2-(3-methylureido)ethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; 2-((6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazol-7-yl)thio)ethyl methylcarbamate; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(2-(2,2,2-trifluoroacetamido)ethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; methyl 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazole-7-carboxylate; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazole-7-carboxylic acid; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(N-methylacetamido)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazole-7-carboxylic acid; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(N-methylacetamido)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(2-methylhydrazineyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; methyl 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido) pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazole-7-carboxylate; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((3-hydroxycyclopentyl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2-hydroxyethyl)(methyl)amino)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((3-hydroxycyclopentyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((3-hydroxycyclobutyl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide; (1 S,2S)-N-(5-(7-(ethyl(methyl)amino)-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-acetyl-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1R,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N,5-trimethyl-1 H-indazole-7-carboxamide; (1R,2S)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2R)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1R,2R)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1R,2R)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-acetyl-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazole-7-carboxamide; (1 S,2S)-N-(5-(7-(ethyl(methyl)amino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethoxy-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 2-((6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazol-7-yl)(methyl)amino)ethyl methylcarbamate; (1 S,2S)-N-(5-(5-chloro-7-(difluoromethyl)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-cyano-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,5-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-(trifluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-cyano-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((cyanomethyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-(trifluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(difluoromethyl)-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(trifluoromethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-methyl-1 H-tetrazol-5-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(pyrimidin-2-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((cyanomethyl)thio)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2R)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(pyrimidin-2-ylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((1-cyanoethyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((2-cyanopropan-2-yl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; 6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N-dimethyl-1 H-indazole-5-carboxamide; (1 S,2S)-N-(5-(5-ethoxy-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((1-cyanocyclopropyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(pyridin-4-ylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-5-ethoxy-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethoxy-6,7-difluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-N-(cyanomethyl)-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N-methyl-1 H-indazole-7-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((5-fluoropyrimidin-2-yl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(pyridin-4-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(N-(cyanomethyl)acetamido)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(2-(pyridin-4-yl)ethyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(1,3,5-triazin-2-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(1,2,4-triazin-3-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(cyclobutyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethylthio)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(isopropyl(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-methyl-2-oxoimidazolidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-methoxyazetidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(cyclopropyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-formyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-(methoxymethyl)azetidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(1,1-dioxidothiomorpholino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(hydroxymethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-methylazetidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-thiomorpholino-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-fluoro-3-methylazetidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((E)-2-cyanovinyl)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(fluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-oxidothiomorpholino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((cyanomethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1 H-pyrrol-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((2-cyanopropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(prop-1-en-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-isopropyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((1-cyanoethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-fluoropyrrolidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; benzyl (5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazol-7-yl)(1-cyanoethyl)carbamate; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(2-methyl-1 H-pyrrol-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (3S,4R)-4-methyltetrahydrofuran-3-yl(5-(5-chloro-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)carbamate; (1 S,2R,3S)-N-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-methyl-3-(1-methyl-1 H-pyrazol-4-yl)cyclopropane-1-carboxamide; 1-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-3-cyclopropylurea; (1 S,2S,3S)-N-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-methyl-3-(1-methyl-1 H-pyrazol-4-yl)cyclopropane-1-carboxamide; 1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1H-indazol-7-yl)-N,N-dimethyl-1 H-pyrrole-3-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-isopropoxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-cyclopentyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-hydroxyethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((1-cyclopropylethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((cyclopropylmethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((R)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((S)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-7-((1,1-difluoropropan-2-yl)amino)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(4-hydroxytetrahydrofuran-2-yl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-formamidoethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-propionamidoethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1H-indazol-7-yl)ethyl)cyclobutanecarboxamide; (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-(2,2,2-trifluoroacetamido)ethyl)-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(7-(1-acetamidoethyl)-5-chloro-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-7-(1,3-dimethylureido)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-chloro-7-(1-(2,2-difluoroacetamido)ethyl)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1S,2S)-N-(5-(5-chloro-7-((1S,2R)-1,2-dimethoxypropyl)-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

19. The compound of claim 15 or a pharmaceutically acceptable salt thereof, which is selected from the group consisting of: (1S,2S)-N-(5-(5-bromo-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-N-(5-(5-ethyl-6-fluoro-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methoxy-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5,7-dichloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5,7-dimethyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-bromo-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-bromo-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-methoxy-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-methoxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-ethoxy-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(diethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((4-(dimethylamino)cyclohexyl)(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((4-hydroxycyclohexyl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl((1R,4R)-4-(methylamino)cyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl((1 S,4S)-4-(methylamino)cyclohexyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide dihydrochloride; (1 S,2S)-N-(5-(7-((4-aminocyclohexyl)(methyl)amino)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((2-hydroxyethyl)thio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-((2-(methylamino)-2-oxoethyl)thio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide bis(2,2,2-trifluoroacetate; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2-hydroxyethyl)thio)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-7-(ethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5,7-bis(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6,7-difluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-(2-hydroxyethoxy)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-ethoxy-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; methyl 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-5-methyl-1 H-indazole-7-carboxylate; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(N-methylacetamido)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(N-methylacetamido)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N-dimethyl-1 H-indazole-7-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2-hydroxyethyl)(methyl)amino)-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((3-hydroxycyclobutyl)(methyl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide; (1 S,2S)-N-(5-(7-(ethyl(methyl)amino)-6-fluoro-5-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,25)-N-(5-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide; 6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N,N,5-trimethyl-1 H-indazole-7-carboxamide; (1R,2S)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2R)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1R,2R)-2-fluoro-N-(5-(6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1R,2R)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(ethyl(methyl)amino)-6-fluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-methyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(difluoromethyl)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-ethyl-6-fluoro-7-(trifluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-cyano-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((cyanomethyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl-7-(trifluoromethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(pyrimidin-2-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((cyanomethyl)thio)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2R)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1R,2S)-N-(5-(6,7-difluoro-5-(methylthio)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-((1-cyanoethyl)thio)-5-ethyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(trifluoromethoxy)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; 5-chloro-N-(cyanomethyl)-6-fluoro-4-(2-((1S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-N-methyl-1H-indazole-7-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(N-(cyanomethyl)acetamido)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(1,3,5-triazin-2-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(methyl(1,2,4-triazin-3-yl)amino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(isopropylamino)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(ethylthio)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-methyl-2-oxoimidazolidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(cyclopropyl(methyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(hydroxymethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(fluoromethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((cyanomethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1 H-pyrrol-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((2-cyanopropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(prop-1-en-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-isopropyl-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((1-cyanoethyl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(3-fluoropyrrolidin-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(2-methyl-1 H-pyrrol-1-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2R,3S)-N-(5-(5-chloro-7-(dimethylamino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-methyl-3-(1-methyl-1 H-pyrazol-4-yl)cyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-isopropoxy-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-cyclopentyl-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(2,2,2-trifluoro-1-hydroxyethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((R)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-((S)-1-methoxypropan-2-yl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-((1,1-difluoropropan-2-yl)amino)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-formamidoethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-propionamidoethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; N-(1-(5-chloro-6-fluoro-4-(2-((1 S,2S)-2-fluorocyclopropane-1-carboxamido)pyrazolo[1,5-a]pyridin-5-yl)-1 H-indazol-7-yl)ethyl)cyclobutanecarboxamide; (1 S,2S)-N-(5-(5-chloro-6-fluoro-7-(1-(2,2,2-trifluoroacetamido)ethyl)-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(7-(1-acetamidoethyl)-5-chloro-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1 S,2S)-N-(5-(5-chloro-7-(1,3-dimethylureido)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1 S,2S)-N-(5-(5-chloro-7-(1-(2,2-difluoroacetamido)ethyl)-6-fluoro-1 H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

Description

DETAILED DESCRIPTION

(1) The following description is merely exemplary in nature and is not intended to limit the present disclosure, application, or uses.

Definitions

(2) The generic terms used in the present disclosure are herein defined for clarity.

(3) This specification uses the terms “substituent”, “radical”, “group”, “moiety”, and “fragment” interchangeably.

(4) As used herein, the term “alkenyl” refers to a straight or branched hydrocarbonyl group with at least one site of unsaturation, i.e., a carbon-carbon, sp2 double bond. In an embodiment, alkenyl has from 2 to 12 carbon atoms. In some embodiments, alkenyl is a C.sub.2-C.sub.10 alkenyl group or a C.sub.2-C.sub.6 alkenyl group. Examples of alkenyl group include, but are not limited to, ethylene or vinyl (—CH═CH.sub.2), allyl (—CH.sub.2CH═CH.sub.2), cyclopentenyl (—C.sub.5H.sub.7), and 5-hexenyl (—CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH═CH.sub.2).

(5) As used herein, the term “alkoxy” is RO— where R is alkyl. Non-limiting examples of alkoxy groups include methoxy, ethoxy and propoxy.

(6) As used herein, the term “alkoxyalkyl” refers to an alkyl moiety substituted with an alkoxy group. Examples of alkoxyalkyl groups include methoxymethyl, methoxyethyl, methoxypropyl and ethoxyethyl.

(7) As used herein, the term “alkoxycarbonyl” is ROC(O)—, where R is an alkyl group as defined herein. In various embodiments, R is a C.sub.1-C.sub.10 alkyl group or a C.sub.1-C.sub.6 alkyl group.

(8) As used herein, the term “alkyl” refers to a straight or branched chain hydrocarbonyl group. In an embodiment, alkyl has from 1 to 12 carbon atoms. In some embodiments, alkyl is a C.sub.1-C.sub.10 alkyl group or a C.sub.1-C.sub.6 alkyl group. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, hexyl, heptyl, octyl, nonyl and decyl. “lower alkyl” means alkyl having from 1 to 4 carbon atoms.

(9) As used herein, if the term “C.sub.1-C.sub.6” is used, it means the number of carbon atoms is from 1 to 6. For example, C.sub.1-C.sub.6 alkyl means an alkyl which carbon number is any integer of from 1 to 6.

(10) As used herein, the term “alkylamino” refers to an amino group substituted with one or more alkyl groups. “N-(alkyl)amino” is RNH— and “N,N-(alkyl).sub.2amino” is R.sub.2N—, where the R groups are alkyl as defined herein and are the same or different. In various embodiments, R is a C.sub.1-C.sub.10 alkyl group or a C.sub.1-C.sub.6 alkyl group. Examples of alkylamino groups include methylamino, ethylamino, propylamino, butylamino, dimethylamino, diethylamino, and methylethylamino.

(11) As used herein, the term “alkylaminoalkyl” refers to an alkyl moiety substituted with an alkylamino group, wherein alkylamino is as defined herein. Examples of alkylaminoakyl groups include methylaminomethyl and ethylaminomethyl.

(12) As used herein, the term “alkynyl” refers to a straight or branched carbon-chain group with at least one site of unsaturation, i.e., a carbon-carbon, sp triple bond. In an embodiment, alkynyl has from 2 to 12 carbon atoms. In some embodiments, alkynyl is a C.sub.2-C.sub.10 alkynyl group or a C.sub.2-C.sub.6alkynyl group. Examples of alkynyl groups include acetylenic (—C≡CH) and propargyl (—CH.sub.2CE CH).

(13) As used herein, the term “aryl” refers to any monocyclic or bicyclic carbon ring of up to 7 atoms in each ring, wherein at least one ring is aromatic, or an aromatic ring system of 5 to 14 carbon atoms which includes a carbocyclic aromatic group fused with a 5- or 6-membered cycloalkyl group. Representative examples of aryl groups include, but are not limited to, phenyl, tolyl, xylyl, naphthyl, tetrahydronaphthyl, anthracenyl, fluorenyl, indenyl, azulenyl and indanyl. A carbocyclic aromatic group can be unsubstituted or optionally substituted.

(14) As used herein, the term “cycloalkyl” is a hydrocarbyl group containing at least one saturated or partially unsaturated ring structure, and attached via a ring carbon. In various embodiments, it refers to a saturated or a partially unsaturated C.sub.3-C.sub.12cyclic moiety, examples of which include cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl and cyclooctyl. “Cycloalkyloxy” is RO—, where R is cycloalkyl.

(15) As used herein, the terms “halogen” and “halo” refers to chloro (—Cl), bromo (—Br), fluoro (—F) or iodo (—I). “Haloalkoxy” refers to an alkoxy group substituted with one or more halo groups and examples of haloalkoxy groups include, but are not limited to, —OCF.sub.3, —OCHF.sub.2 and —OCH.sub.2F. “Haloalkoxyalkyl” refers to an alkyl moiety substituted with a haloalkoxy group, wherein haloalkoxy is as defined herein. Examples of haloalkoxyalkyl groups include trifluoromethoxymethyl, trifluoroethoxymethyl and trifluoromethoxyethyl. “Haloalkyl” refers to an alkyl moiety substituted with one or more halo groups. Examples of haloalkyl groups include —CF.sub.3 and —CHF.sub.2.

(16) As used herein, the term “heteroalkyl” refers to a straight- or branched-chain alkyl group having from 2 to 14 carbons (in some embodiments, 2 to 10 carbons) in the chain, one or more of which has been replaced by a heteroatom selected from S, O, P and N. Exemplary heteroalkyls include alkyl ethers, secondary and tertiary alkyl amines, amides, alkyl sulfides, and the like.

(17) As used herein, the term “heterocyclyl” includes the heteroaryls defined below and refers to a saturated or partially unsaturated monocyclic, bicyclic or tricyclic group of 2 to 14 ring-carbon atoms and, in addition to ring-carbon atoms, 1 to 4 heteroatoms selected from P, N, O and S. In various embodiments the heterocyclic group is attached to another moiety through carbon or through a heteroatom, and is optionally substituted on carbon or a heteroatom. Examples of heterocyclyl include azetidinyl, benzoimidazolyl, benzofuranyl, benzofurazanyl, benzopyrazolyl, benzotriazolyl, benzothiophenyl, benzoxazolyl, carbazolyl, carbolinyl, cinnolinyl, furanyl, imidazolyl, indolinyl, indolyl, indolazinyl, indazolyl, isobenzofuranyl, isoindolyl, isoquinolyl, isothiazolyl, isoxazolyl, naphthpyridinyl, oxadiazolyl, oxazolyl, oxazoline, isoxazoline, oxetanyl, pyranyl, pyrazinyl, pyrazolyl, pyridazinyl, pyridopyridinyl, pyridazinyl, pyridyl, pyrimidyl, pyrrolyl, quinazolinyl, quinolyl, quinoxalinyl, tetrahydropyranyl, tetrahydrothiopyranyl, tetrahydroisoquinolinyl, tetrazolyl, tetrazolopyridyl, thiadiazolyl, thiazolyl, thienyl, triazolyl, azetidinyl, 1,4-dioxanyl, hexahydroazepinyl, piperazinyl, piperidinyl, pyridin-2-onyl, pyrrolidinyl, morpholinyl, thiomorpholinyl, dihydrobenzoimidazolyl, dihydrobenzofuranyl, dihydrobenzothiophenyl, dihydrobenzoxazolyl, dihydrofuranyl, dihydroimidazolyl, dihydroindolyl, dihydroisooxazolyl, dihydroisothiazolyl, dihydrooxadiazolyl, dihydrooxazolyl, dihydropyrazinyl, dihydropyrazolyl, dihydropyridinyl, dihydropyrimidinyl, dihydropyrrolyl, dihydroquinolinyl, dihydrotetrazolyl, dihydrothiadiazolyl, dihydrothiazolyl, dihydrothienyl, dihydrotriazolyl, dihydroazetidinyl, methylenedioxybenzoyl, tetrahydrofuranyl, and tetrahydrothienyl, and N-oxides thereof “Heterocyclyloxy” is RO—, where R is heterocyclyl. “Heterocyclylthio” is RS—, where R is heterocyclyl.

(18) As used herein, the term “3- or 4-membered heterocyclyl” refers to a monocyclic ring having 3 or 4 ring atoms wherein at least one ring atom is heteroatom selected from the group consisting of N, O and S. Non-limiting examples of 3- or 4-membered heterocyclyl include aziridinyl, 2H-azirinyl, oxiranyl, thiiranyl, azetidinyl, 2,3-dihyroazetyl, azetyl, 1,3-diazetidinyl, oxetanyl, 2H-oxetyl, thietanyl, and 2H-thietyl.

(19) As used herein, the term “heteroaryl” refers to a monocyclic, bicyclic or tricyclic ring having up to 7 atoms in each ring, wherein at least one ring is aromatic and contains from 1 to 4 heteroatoms in the ring selected from the group consisting of N, O and S. Non-limiting examples of heteroaryl include pyridyl, thienyl, furanyl, pyrimidyl, imidazolyl, pyranyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, oxazolyl, isoxazoyl, pyrrolyl, pyridazinyl, pyrazinyl, quinolinyl, isoquinolinyl, benzofuranyl, dibenzofuranyl, dibenzothiophenyl, benzothienyl, indolyl, benzothiazolyl, benzooxazolyl, benzimidazolyl, isoindolyl, benzotriazolyl, purinyl, thianaphthenyl and pyrazinyl. Attachment of heteroaryl can occur via an aromatic ring, or, if heteroaryl is bicyclic or tricyclic and one of the rings is not aromatic or contains no heteroatoms, through a non-aromatic ring or a ring containing no heteroatoms. “Heteroaryl” is also understood to include the N-oxide derivative of any nitrogen containing heteroaryl. “Heteroaryloxy” is RO—, where R is heteroaryl.

(20) As used herein, the term “hydroxyalkoxy” refers to an alkoxy group substituted with a hydroxyl group (—OH), wherein alkoxy is as defined herein. An example of hydroxyalkoxy is hydroxyethoxy.

(21) As used herein, the term “hydroxyalkyl” refers to a linear or branched monovalent C.sub.1-C.sub.10 hydrocarbon group substituted with at least one hydroxy group and examples of hydroxyalkyl groups include, but are not limited to, hydroxymethyl, hydroxyethyl, hydroxypropyl and hydroxybutyl.

(22) As used herein, the term “pharmaceutically acceptable” means suitable for use in pharmaceutical preparations, generally considered as safe for such use, officially approved by a regulatory agency of a national or state government for such use, or being listed in the U.S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, and more particularly in humans.

(23) As used herein, the term “pharmaceutically acceptable carrier” refers to a diluent, adjuvant, excipient, or carrier, or other ingredient which is pharmaceutically acceptable and with which a compound of the invention is administered.

(24) As used herein, the term “pharmaceutically acceptable salt” refers to a salt which may enhance desired pharmacological activity. Examples of pharmaceutically acceptable salts include acid addition salts formed with inorganic or organic acids, metal salts and amine salts. Examples of acid addition salts formed with inorganic acids include salts with hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid and phosphoric acid. Examples of acid addition salts formed with organic acids such as acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, o-(4-hydroxy-benzoyl)-benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethane-sulfonic acid, benzenesulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, 4-methyl-bicyclo[2.2.2]oct-2-ene1-carboxylic acid, gluco-heptonic acid, 4,4′-methylenebis(3-hydroxy-2-naphthoic) acid, 3-phenylpropionic acid, trimethyl-acetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxy-naphthoic acids, salicylic acid, stearic acid and muconic acid. Examples of metal salts include salts with sodium, potassium, calcium, magnesium, aluminum, iron, and zinc ions. Examples of amine salts include salts with ammonia and organic nitrogenous bases strong enough to form salts with carboxylic acids.

(25) As used herein, the term “substituted” means any of above groups (i.e., alkyl, aryl, heteroaryl, heterocycle or cycloalkyl) wherein at least one hydrogen atom of the moiety being substituted is replaced with a substituent. In one embodiment, each carbon atom of the group being substituted is substituted with no more than two substituents. In another embodiment, each carbon atom of the group being substituted is substituted with no more than one substituent. In the case of a keto substituent, two hydrogen atoms are replaced with an oxygen which is attached to the carbon via a double bond. Unless specifically defined, substituents include halo, hydroxyl, (lower) alkyl, haloalkyl, mono- or di-alkylamino, aryl, heterocycle, —NO.sub.2, B(OH).sub.2, BPin, —NR.sub.aR.sub.b, —NR.sub.aC(═O)R.sub.b, —NR.sub.aC(═O)NR.sub.aR.sub.b, —NR.sub.aC(═O)OR.sub.b, —NR.sub.aSO.sub.2R.sub.b, —OR.sub.a, —CN, —C(═O)R.sub.a, —C(═O)OR.sub.a, —C(═O)NR.sub.aR.sub.b, —OC(═O)R.sub.a, —OC(═O)OR.sub.a, —OC(═O)NR.sub.aR.sub.b, —NR.sub.aSO.sub.2R.sub.b, —PO.sub.3R.sub.a, —PO(OR.sub.a)(OR.sub.b), —SO.sub.2R.sub.a, —S(O)R.sub.a, —SO(N)R.sub.a (e.g., sulfoximine), —(R.sub.a)S═NR.sub.b (e.g., sulfilimine) and —SR.sub.a, wherein R.sub.a and R.sub.b are the same or different and independently —H, halo, amino, alkyl, haloalkyl, aryl or heterocycle, or wherein R.sub.a and R.sub.b taken together with the nitrogen atom to which they are attached form a heterocycle. R.sub.a and R.sub.b may be in the plural based on atoms which those are attached to.

(26) As used herein, the term “therapeutically effective amount” means when applied to a compound of the invention is intended to denote an amount of the compound that is sufficient to ameliorate, palliate, stabilize, reverse, slow or delay the progression of a disorder or disease state, or of a symptom of the disorder or disease. In an embodiment, the method of the present invention provides for administration of combinations of compounds. In such instances, the “therapeutically effective amount” is the amount of a compound of the present invention in the combination sufficient to cause the intended biological effect.

(27) As used herein, the term “treatment” or “treating” as used herein means ameliorating or reversing the progress or severity of a disease or disorder, or ameliorating or reversing one or more symptoms or side effects of such disease or disorder. “Treatment” or “treating”, as used herein, also means to inhibit or block, as in retard, arrest, restrain, impede or obstruct, the progress of a system, condition or state of a disease or disorder. For purposes of this invention, “treatment” or “treating” further means an approach for obtaining beneficial or desired clinical results, where “beneficial or desired clinical results” include, without limitation, alleviation of a symptom, diminishment of the extent of a disorder or disease, stabilized (i.e., not worsening) disease or disorder state, delay or slowing of a disease or disorder state, amelioration or palliation of a disease or disorder state, and remission of a disease or disorder, whether partial or total.

(28) Compounds

(29) The present disclosure provides a compound of Formula (I):

(30) ##STR00003##
or a pharmaceutically acceptable salt, hydrate, or solvate, thereof, wherein: X is O or S; L is a bond, —O—, —S—, or —NR.sup.6—; R.sup.1 is alkyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl, wherein R.sup.1 is optionally substituted with one or more substituents independently selected from R.sup.7; R.sup.6 is —H or C.sub.1-6 alkyl; R.sup.7 is C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, oxo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13; R.sup.9 is —H, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl; Each R.sup.10 and R.sup.11 is independently —H, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl, or R.sup.10 and R.sup.11 are taken together with the nitrogen atom to which they are attached to form a 4- to 12-membered heterocyclyl optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; Each R.sup.12 and R.sup.13 is independently C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.3-8 cycloalkyl, aryl, heteroaryl, heterocyclyl, or R.sup.12 and R.sup.13 are taken together with the phosphorus atom to which they are attached to form a 4- to 8-membered heterocyclyl optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; Het is selected from the group consisting of:

(31) ##STR00004## Each of R.sup.a, R.sup.b and R.sup.c is independently —H, -D, halo, CF.sub.3, CF.sub.2H, CH.sub.2F, CN, OR.sup.9 or NR.sup.10R.sup.11; R.sup.2 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, hydroxyl, —CD.sub.2OH, —CN, —NO.sub.2, haloalkyl, trimethylsilylethoxymethyl, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sub.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13 wherein the C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; R.sup.3 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —CH.sub.2OH, —CD.sub.2OH, —OH, —CN, —NO.sub.2, haloalkyl, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —SR.sup.9, —S(O)R.sup.9, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sub.10, —S(O).sub.2NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, —N(R.sup.6)C(O)NR.sup.10R.sup.11, —N(R.sup.6)S(O).sub.2R.sup.9, —N(R.sup.6)S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13; M is a bond, —O—, —S—, or —NR.sup.6—; R.sup.6 is —H or C.sub.1-6 alkyl; R.sup.4 is —H, -D, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, —S(O).sub.2NR.sup.10R.sup.11, or —P(O)R.sup.12R.sup.13, wherein C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxyl, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —CD.sub.3, —NO.sub.2, —NR.sup.10R.sup.11, —NR.sup.10C(═O)R.sup.9, —NR.sup.10C(═O)NR.sup.10R.sup.11, —NR.sup.10C(═O)OR.sup.9, —NR.sup.10S(O).sub.2R.sup.9, —OR.sup.9, —C(═O)R.sup.9, —C(═O)OR.sup.9, —C(═O)NR.sup.10R.sup.11, —OC(═O)R.sup.9, —OC(═O)OR.sup.9, and —OC(═O)NR.sup.10R.sup.11; and R.sup.5 is —H, -D, —CD.sub.3, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, hydroxyl, —CH.sub.2OH, —CD.sub.2OH, —CN or haloalkyl.

(32) In various embodiments, L is a bond, and R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, and —N(R.sup.6)C(O)NR.sup.10R.sup.11. In various embodiments, each of R.sup.2 and R.sup.3 is independently —H, halo, alkylthio, haloalkyl, or alkyl. In various embodiments, M is a bond, —O—, or —NR.sup.6—; and R.sup.4 is —H, -D, C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, heterocyclyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)NR.sup.10R.sup.11, —S(O).sub.2R.sup.9, —S(O)(═NH)R.sup.10, or —S(O).sub.2NR.sup.10R.sup.11, wherein the C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, aryl, heteroaryl, or heterocyclyl is optionally substituted with one or more groups selected from the group consisting of halo, hydroxy, alkyl, alkenyl, alkynyl, haloalkyl, hydroxyalkyl, —CN, —CD.sub.3, —NR.sup.10R.sup.11, —NR.sup.10S(O).sub.2R.sup.9, and —NR.sup.10C(═O)R.sup.9.

(33) In another embodiment, there is provided a compound represented by Formula (II):

(34) ##STR00005##

(35) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.a, R.sup.b, M, and L are as defined above for Formula (I).

(36) In various embodiments, L is a bond, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkylthio, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, cyanoalkyl, dimethylamino, dimethylaminoethyl, dimethylaminocarbonyl, methylaminooxoethyl, aminocarbonylalkyl, acetamindoethyl, propionamidoethyl, formamidoethyl, aminoalkyl, methylaminocarbonylmethyl, alkoxyalkyl, azetidinyl, or azetidinylmethyl; and R.sup.5 is —H, alkyl, or halo.

(37) Non-limiting exemplary compounds of Formula (II) include the compound of Examples 1-145 of Table 1. In particular embodiments, the compound is selected from the group consisting of: the compounds of Examples 58, 80, 82, 85, 87, 92, 94, 97, 98, 110, 111, 118, 123, 125, 129, and 134.

(38) In another embodiment, there is provided a compound represented by Formula (III):

(39) ##STR00006##

(40) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.a, R.sup.b, M, and L are as defined above for Formula (I).

(41) In some embodiments, L is a bond, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, dimethylamino, dimethylaminoethyl, dimethylaminocarbonyl, methylaminooxoethyl, aminocarbonylalkyl, acetamindoethyl, or alkoxyalkyl; and R.sup.5 is —H, alkyl, or halo.

(42) Non-limiting exemplary compounds of Formula (III) include the compound of Examples 146-218 of Table 1. In particular embodiments, the compound is selected from the group consisting of the compounds of Examples 149, 152, 156, 159, 161-163, 167, 169, 170, 172-175, 178, 184, 193, 194, 196, 199, and 218.

(43) In another embodiment, there is provided a compound represented by Formula (IV):

(44) ##STR00007##

(45) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.a, R.sup.b, M, and L are as defined above for Formula (I).

(46) In some embodiments, L is a bond, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, cyanoalkyl, dimethylamino, dimethylaminoethyl, dimethylaminocarbonyl, methylaminooxoethyl, aminocarbonylalkyl, acetamindoethyl, propionamidoethyl, formamidoethyl, cycloalkylalkyl, cycloalkyl(hydroxy)alkyl, hydroxycycloalkyl, methoxycycloalkyl, cycloalkyl(methoxy)methyl, alkoxyalkyl, alkenyl, methylsulfonamidoethyl, imidazolylethyl, dioxanyl, cyclobutanylcarbonylaminoethyl, difluoroacetamidoethyl, trifluoroacetamidoethyl, methylthiomethyl, methylthioethyl, azetidinyl, azetidinylmethyl, cyclopropylcarbonylamino(cyano)methyl, cyano(difluoroacetamido)methyl, propanyl-1,1,1,3,3,3-d6)amino, tetrahydrofuranyl, methylimidazolylethyl, furanyl, pyrrolyl, methylpyrrolyl, isoxazolyl, tetrazolylalkyl, methylpyrazolyl, or methylpyrazolylmethyl; and R.sup.5 is —H, alkyl, or halo.

(47) Non-limiting exemplary compounds of Formula (IV) include the compound of Examples 219 and 220 of Table 1.

(48) In another embodiment, there is provided a compound represented by Formula (V):

(49) ##STR00008##

(50) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.a, R.sup.b, M, and L are as defined above for Formula (I).

(51) In some embodiments, L is a bond, and R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of C.sub.1-6 alkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, cycloalkyl, halo, cyano, hydroxy, —C(O)R.sup.9, —C(O)OR.sup.9, —C(O)NR.sup.10R.sup.11, —OR.sup.9, —OC(O)R.sup.9, —OC(O)NR.sup.10R.sup.11, —NR.sup.10R.sup.11, —N(R.sup.6)NR.sup.10R.sup.11, —N(R.sup.6)OR.sup.9, —N(R.sup.6)C(O)R.sup.9, —N(R.sup.6)C(O)OR.sup.9, and —N(R.sup.6)C(O)NR.sup.10R.sup.11. In some other embodiments, R.sup.1 is cycloalkyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl.

(52) Non-limiting exemplary compounds of Formula (V) include the compound of Examples 221-445 of Table 1.

(53) In some embodiments, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-C.sub.3 alkyl, C.sub.1-C.sub.3 hydroxyalkyl and C.sub.1-C.sub.3 haloalkyl; R.sup.2 is —H, alkyl, alkylthio, haloalkyl, or halo; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, monoalkylamino, or dialkylamino; R.sup.5 is —H, alkyl, or halo. Non-limiting exemplary compounds include one selected from the group consisting of: (1S,2S)—N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)—N-(6-(7-(dimethylamino)-6-fluoro-5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)—N-(6-(7-(dimethylamino)-6-fluoro-5-(methylthio)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)—N-(6-(7-(dimethylamino)-6-fluoro-5-(trifluoromethyl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; (1S,2S)—N-(6-(5-chloro-6-fluoro-7-(isopropylamino)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide; and (1S,2S)—N-(6-(5-chloro-6-fluoro-7-isopropyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide.

(54) In some embodiments, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, monoalkylamino, or dialkylamino; and R.sup.5 is —H, alkyl, or halo. Non-limiting exemplary compounds include one selected from the group consisting of: the compounds of Examples 258, 261, 265, 266, 269, 272, 275, 280, 288, 291, 293, 296, 297, 300, 304, 306, 310, 318, 320, 324, 327, 329, 330, 332, 334, 336, 341, 345, 349, 353, 356, 358, 359, 361, 366, 371, 372, 374, 390, 391, 393, 404, 405, 408, 410, 414, 417, 419, 422, 423, 425, 426, 428, 430, 433, 434, 436, 439, 441, and 445.

(55) In some embodiments, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, alkylcarbonyl, dialkylaminocarbonyl, oxopyrrolidinyl, hydroxyalkyl, haloalkyl, haloalkenyl, cycloalkyl, pyridinyl, monoalkylamino, or dialkylamino; and R.sup.5 is —H, alkyl, or halo. Non-limiting exemplary compounds include one selected from the group consisting of the compounds of Examples 258, 261, 265, 266, 268, 269, 271-273 275, 280, 281, 288, 290, 291, 293, 296-298, 300, 304, 306, 307, 310, 316, 318, 320, 324, 326, 327, 329, 330-334, 336, 339, 341, 345, 346, 349, 353, 356, 358, 359, 361-363, 365-367, 370-374, 377-379, 383, 388, 390, 391, 393, 398, 401, 404-406, 408-410, 414, 415, 417, 419, 421-426, 428, 430, 433, 434, 436, 439, 441, and 445.

(56) In another embodiment, there is provided a compound represented by Formula (VI):

(57) ##STR00009##

(58) wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.a, R.sup.b, M, and L are as defined above for Formula (I).

(59) In some embodiments, L is a bond, R.sup.1 is cyclopropyl which is optionally substituted with one or more groups selected from the group consisting of halo, C.sub.1-3 alkyl, C.sub.1-3 hydroxyalkyl and C.sub.1-3 haloalkyl; R.sup.2 is —H, alkyl, halo, haloalkyl, or alkylthio; R.sup.3 is —H, alkyl, or halo; M is a bond, —O—, —S— or —NR.sup.6—; R.sup.4 is —H, halo, alkyl, hydroxyalkyl, haloalkyl, haloalkylamidoalkyl, haloalkylcarbonylaminoalkyl, alkylamidoalkyl, hydroxyhaloalkyl, haloalkenyl, cycloalkyl, cyano, cyanoalkyl, dimethylamino, dimethylaminoethyl, methylaminocarbonyl, dimethylaminocarbonyl, methylaminooxoethyl, aminocarbonylalkyl, acetamindoethyl, dialkylaminocycloalkyl, aminocycloalkyl, methylaminocycloalkyl, cycloalkylalkyl, cycloalkyl(hydroxy)alkyl, cycloalkylamidoalkyl, cycloalkylaminocarbonyl, hydroxycycloalkyl, methoxycycloalkyl, cycloalkyl(methoxy)methyl, alkoxycarbonyl, alkylcarbonyl, alkylamidoalkyl, alkoxyalkyl, alkenyl, methylsulfonamidoethyl, imidazolylethyl, dioxanyl, azetidinyl, azetidinylmethyl, tetrahydrofuranyl, furanyl, pyrimidinyl, pyridinyl, pyrrolyl, halopyrrolidinyl, pyrrolidinyl, methylpyrrolyl, isoxazolyl, tetrazolylalkyl, triazinyl, methylpyrazolyl, or methylpyrazolylmethyl; and R.sup.5 is —H, alkyl, or halo.

(60) Non-limiting exemplary compounds of Formula (VI) include the compound of Examples 446-666 of Table 1. In particular embodiments, the compound is selected from the group consisting of the compounds of Examples 464, 466, 467, 476, 477, 480, 484, 485, 487, 488, 490-494, 496, 497, 502-505, 509, 513, 514, 519-521, 523-525, 529-532, 534, 541, 543, 548, 550, 552, 556-558, 561-565, 568-574, 577, 579, 581, 585, 586, 588, 592, 596-600, 602, 607, 612, 615, 617-619, 621, 623, 625, 629, 634, 636-642, 644, 646, 650-652, 655-657, and 659-665.

(61) In an embodiment, there is provided a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and a compound of Formula (I) or a pharmaceutically acceptable salt thereof.

(62) Medical Uses and Methods of Treatment Using the Compounds

(63) The present disclosure provides a method of treating a subject with a disease or disorder associated with modulation of HPK1 comprising: administering to the subject in need thereof a therapeutically effective amount of the compound of Formula (I) or a pharmaceutically acceptable salt thereof. In some embodiments, the disease or disorder associated with modulation of HPK1 is a cancer, metastasis, inflammation, or immune disease including autoimmune disease.

(64) In some other embodiments, the disease is cancer, metastasis, inflammation or auto-immune disease. In particular embodiments, the cancer is selected from the group consisting of carcinomas, melanomas, blastomas, sarcomas, lymphomas and leukemias, including without limitation, bladder carcinoma, brain tumors, breast cancer, cervical cancer, colorectal cancer, esophageal cancer, endometrial cancer, hepatocellular carcinoma, laryngeal cancer, lung cancer, osteosarcoma, ovarian cancer, pancreatic cancer, prostate cancer, renal carcinoma and thyroid cancer, acute lymphocytic leukemia, acute myeloid leukemia, ependymoma, Ewing's sarcoma, glioblastoma, medulloblastoma, neuroblastoma, osteosarcoma, rhabdomyosarcoma, rhabdoid cancer, and nephroblastoma (Wilm's tumor).

(65) In some embodiments, the autoimmune disease is an inflammatory bowel disease, Addison's disease, alopecia areata, ankylosing spondylitis, antiphospholipid syndrome, hemolytic anemia, autoimmune hepatitis, Behcet's disease, Berger's disease, bullous pemphigoid, cardiomyopathy, celiac sprue, chronic fatigue immune dysfunction syndrome (CFIDS), chronic inflammatory demyelinating polyneuropathy, Churg-Strauss syndrome, cicatricial pemphigoid, cold agglutinin disease, type 1 diabetes, discoid lupus, essential mixed cryoglobulinemia, Graves' disease, Guillain-Barre syndrome, Hashimoto's thyroiditis, hypothyroidism, autoimmune lymphoproliferative syndrome (ALPS), idiopathic pulmonary fibrosis, idiopathic thrombocytopenia purpura (ITP), juvenile arthritis, lichen planus, lupus erythematosus, Meniere's disease, mixed connective tissue disease, multiple sclerosis, myasthenia gravis, pemphigus vulgaris, pernicious anemia, polychondritis, autoimmune polyglandular syndromes, polymyalgia rheumatica, polymyositis, dermatomyositis, primary agammaglobulinemia, primary biliary cirrhosis, psoriasis, psoriatic arthritis, Raynaud's phenomenon, Reiter's syndrome, rheumatic fever, rheumatoid arthritis, sarcoidosis, scleroderma, Sjogren's syndrome, stiff-man syndrome, Takayasu arteritis, giant cell arteritis, ulcerative colitis, uveitis, vasculitis, or granulomatosis with polyangiitis.

(66) In another embodiment, there is provided the use of a compound of Formula (I) or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for inhibiting HPK1 activity in a subject in need of inhibition of HPK1 activity. In some embodiments, the use includes treatment of cancer.

(67) Suitable subjects to be treated according to the present disclosure include mammalian subjects. Mammals according to the present disclosure include, but are not limited to, human, canine, feline, bovine, caprine, equine, ovine, porcine, rodents, lagomorphs, primates, and the like, and encompass mammals in utero. Subjects may be of either gender and at any stage of development. In one embodiment, the suitable subject to be treated according to the present disclosure is human.

(68) The compounds of the present disclosure are generally administered in a therapeutically effective amount. The compounds of the present disclosure can be administered by any suitable route in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended. An effective dosage is typically in the range of about 0.01 to about 1000 mg per kg body weight per day, preferably about 0.01 to about 500 mg/kg/day, in single or divided doses. Depending on age, species and disease or condition being treated, dosage levels below the lower limit of this range may be suitable. In other cases, still larger doses may be used without harmful side effects. Larger doses may also be divided into several smaller doses, for administration throughout the day. Methods for determining suitable doses are well known in the art to which the present disclosure pertains. For example, Remington: The Science and Practice of Pharmacy, Mack Publishing Co., 20.sup.th ed., 2000 can be used.

(69) Pharmaceutical Compositions, Dosage Forms and Administration Routes

(70) For the treatment of the diseases or conditions referred to above, the compounds described herein or pharmaceutically acceptable salts thereof can be administered as follows:

(71) Oral Administration

(72) The compounds of the present disclosure may be administered orally, including by swallowing, so that the compound enters the gastrointestinal tract, or absorbed into the blood stream directly from the mouth (e.g., buccal or sublingual administration). Suitable compositions for oral administration include solid, liquid, gel or powder formulations, and have a dosage form such as tablet, lozenge, capsule, granule or powder. Compositions for oral administration may be formulated as immediate or modified release, including delayed or sustained release, optionally with enteric coating. Liquid formulations can include solutions, syrups and suspensions, which can be used in soft or hard capsules. Such formulations may include a pharmaceutically acceptable carrier, for example, water, ethanol, polyethylene glycol, cellulose, or an oil. The formulation may also include one or more emulsifying agents and/or suspending agents.

(73) In a tablet dosage form the amount of drug present may be from about 0.05% to about 95% by weight, more typically from about 2% to about 50% by weight of the dosage form. In addition, tablets may contain a disintegrant, comprising from about 0.5% to about 35% by weight, more typically from about 2% to about 25% of the dosage form. Examples of disintegrants include, but are not limited to, lactose, starch, sodium starch glycolate, crospovidone, croscarmellose sodium, maltodextrin, or mixtures thereof.

(74) Suitable lubricants, for use in a tablet, may be present in amounts from about 0.1% to about 5% by weight, and include, but are not limited to, talc, silicon dioxide, stearic acid, calcium, zinc or magnesium stearate, sodium stearyl fumarate and the like.

(75) Suitable binders, for use in a tablet, include, but are not limited to, gelatin, polyethylene glycol, sugars, gums, starch, polyvinyl pyrrolidone, hydroxypropyl cellulose, hydroxypropylmethyl cellulose and the like. Suitable diluents, for use in a tablet, include, but are not limited to, mannitol, xylitol, lactose, dextrose, sucrose, sorbitol, microcrystalline cellulose and starch.

(76) Suitable solubilizers, for use in a tablet, may be present in amounts from about 0.1% to about 3% by weight, and include, but are not limited to, polysorbates, sodium lauryl sulfate, sodium dodecyl sulfate, propylene carbonate, diethyleneglycol monoethyl ether, dimethyl isosorbide, polyethylene glycol (natural or hydrogenated) castor oil, HCOR™ (Nikkol), oleyl ester, Gelucire™, caprylic/caprylic acid mono/diglyceride, sorbitan fatty acid esters, and Solutol HS™.

(77) Parenteral Administration

(78) Compounds of the present disclosure may be administered directly into the blood stream, muscle, or internal organs. Suitable means for parenteral administration include intravenous, intra-muscular, subcutaneous intraarterial, intraperitoneal, intrathecal, intracranial, and the like. Suitable devices for parenteral administration include injectors (including needle and needle-free injectors) and infusion methods.

(79) Compositions for parenteral administration may be formulated as immediate or modified release, including delayed or sustained release. Most parenteral formulations are aqueous solutions containing excipients, including salts, buffering agents and isotonic agents. Parenteral formulations may also be prepared in a dehydrated form (e.g., by lyophilization) or as sterile non-aqueous solutions. These formulations can be used with a suitable vehicle, such as sterile water. Solubility-enhancing agents may also be used in preparation of parenteral solutions.

(80) Transdermal Administration

(81) Compounds of the present disclosure may be administered topically to the skin or transdermally. Formulations for this topical administration can include lotions, solutions, creams, gels, hydrogels, ointments, foams, implants, patches and the like. Pharmaceutically acceptable carriers for topical administration formulations can include water, alcohol, mineral oil, glycerin, polyethylene glycol and the like. Topical or transdermal administration can also be performed by electroporation, iontophoresis, phonophoresis and the like. Compositions for topical administration may be formulated as immediate or modified release, including delayed or sustained release.

(82) Combination Therapy

(83) A pharmaceutical composition according to the present disclosure may contain one or more additional therapeutic agents, for example, to increase the efficacy or decrease the side effects. In some embodiments, accordingly, a pharmaceutical composition further contains one or more additional therapeutic agents selected from active ingredients useful to treat or inhibit diseases mediated directly or indirectly by HPK1. Examples of such active ingredients are, without limitation, agents to treat cancer, metastasis, inflammation, or auto-immune pathogenesis. In some embodiments, the compound of Formula (I) is administered with anti-PD-1 agent, anti-PD-L1 agent, or anti-CTLA4 agent.

(84) References for Preparing Pharmaceutical Compositions

(85) Methods for preparing pharmaceutical compositions for treating or preventing a disease or condition are well known in the art to which the present disclosure pertains. For example, based on Handbook of Pharmaceutical Excipients (7.sup.th ed.), Remington: The Science and Practice of Pharmacy (20.sup.th ed.), Encyclopedia of Pharmaceutical Technology (3.sup.rd ed.), or Sustained and Controlled Release Drug Delivery Systems (1978), pharmaceutically acceptable excipients, carriers, additives and so on can be selected and then mixed with the compounds of the present disclosure for making the pharmaceutical compositions.

(86) The present disclosure provides a compound having various pharmacological effects by inhibiting HPK1 activity, a pharmaceutical composition having the compound as an effective agent, a medical use, particularly for treating a disease or disorder modulated by HPK1, of the compound, and a method of treatment or prevention comprising administering the compound to a subject in need of such treatment or prevention. The compounds of the present disclosure and pharmaceutically acceptable salts thereof have good safety and high selectivity for HPK1, and thus exhibit superior property as a drug.

(87) Compound Preparation

(88) The following Preparative Examples illustrate the preparation of intermediate compounds that are useful for preparing compounds of formula (I). The novel intermediate compounds described herein, as well as the synthetic processes useful for preparing the intermediate compounds represent embodiments of the current invention.

Intermediate 1A. 1-(tetrahydro-2H-pyran-2-yl)-5-(thiophen-2-yl)-1H-indazol-4-yl trifluoromethanesulfonate

(89) ##STR00010##

Step 1) 3-bromo-4-chloro-5-fluoro-2-methylaniline

(90) To a solution of 3-bromo-5-fluoro-2-methylaniline (50 g, 245 mmol, 1 eq) in AcOH (100 mL) was added N-chlorosuccinimide (36 g, 270 mmol, 1.1 eq). The mixture was stirred at 25° C. for 16 hr. The mixture was concentrated under vacuum and the residue was extracted with Dichloromethane (200 mL*2). The combined organic layers were washed with sat. NaHCO.sub.3 200 mL, dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The crude product (66 g, crude) was obtained as a black oil.

Step 2) 4-bromo-5-chloro-6-fluoro-1H-indazole

(91) To a solution of 3-bromo-4-chloro-5-fluoro-2-methylaniline (25.8 g, 108 mmol, 1 eq) in AcOH (1.96 L, 0.05 M), H.sub.2O (0.065 L, 1.5 M) was added sodium nitrite (8.96 g, 130 mmol, 1.2 eq). The mixture was stirred at 25° C. for 16 hr. The mixture was concentrated under vacuum and the residue was extracted with Dichloromethane (1 L*2). The combined organic layers were washed with sat. NaHCO.sub.3 (1 L), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The crude product (23.6 g, crude) was obtained as a brown solid.

Step 3) 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(92) To a solution of 4-bromo-5-chloro-6-fluoro-1H-indazole (1.98 g, 7.97 mmol, 1 eq) in THP (40 mL) was added 3,4-dihydro-2H-pyran (2.18 ml, 23.9 mmol, 3 eq) and p-toluenesulfonic acid monohydrate (300 mg, 1.59 mmol, 0.2 eq). The reaction mixture was stirred 70° C. for 14 hours. The reaction mixture was extracted with Ethyl Acetate and dried over MgSO.sub.4. The organic residue was purified by column chromatography (silical gel, Hex:Ethyl acetate=1:0 to 4:1). 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (1.51 g, 4.54 mmol, 57% yield) was obtained.

(93) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.16 (s, 1H), 8.00 (dd, J=9.3, 1.1 Hz, 1H), 5.85 (dd, J=9.6, 2.5 Hz, 1H), 3.87 (d, J=12.6 Hz, 1H), 3.79-3.72 (m, 1H), 2.38-2.30 (m, 1H), 2.04-1.94 (m, 2H), 1.77-1.55 (m, 3H).

Intermediate 1B. 4-bromo-5-chloro-6-fluoro-7-iodo-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole

(94) ##STR00011##

Step 1) 4-bromo-5-chloro-6-fluoro-7-iodo-1H-indazole

(95) To a solution of 4-bromo-5-chloro-6-fluoro-1H-indazole (2 g, 8.02 mmol) in sulfuric acid (1.7 mL) was added N-iodosuccinimide (2.7 g, 12.03 mmol) portionwise. The mixture was stirred at 0° C. for 3 h. After the reaction completed, the mixture was poured into ice water and quenched by solid NaOH and then extracted with Dichloromethane. The combined organic residue was concentrated in vacuo. (2.99 g, crude).

(96) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.91 (s, 1H), 8.27 (d, J=1.6 Hz, 1H).

Step 2) 4-bromo-5-chloro-6-fluoro-7-iodo-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole

(97) To a solution of 4-bromo-5-chloro-6-fluoro-7-iodo-1H-indazole (2.99 g, 7.97 mmol, 1 eq) in THF (40 mL) was added 3,4-dihydro-2H-pyran (2.18 ml, 23.9 mmol, 3 eq) and p-toluenesulfonic acid monohydrate (300 mg, 1.59 mmol, 0.2 eq). The reaction mixture was stirred 60° C. for 16 hours. The reaction mixture was extracted with Ethyl Acetate and dried over MgSO.sub.4. The organic residue was purified by column chromatography (silical gel, Hex:Ethyl acetate=1:0 to 4:1). 4-bromo-5-chloro-6-fluoro-7-iodo-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole (1.64 g, 7.97 mmol, 60.7% yield) was obtained.

(98) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.84 (s, 1H), 5.80 (dd, J=9.9, 2.7 Hz, 1H), 5.66 (s, 1H), 4.02 (t, J=6.6 Hz, 1H), 3.85-3.70 (m, 1H), 2.33-2.21 (m, 1H), 2.08-1.91 (m, 2H), 1.79-1.45 (m, 4H).

Intermediate 1C. 4-bromo-5-chloro-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-7-amine

(99) ##STR00012##

Step 1) 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole

(100) To a mixture of HNO.sub.3 (12.63 g, 200.43 mmol, 9.02 mL, 5 eq) in H.sub.2SO.sub.4 (50 mL) stirred at 0° C. was added 4-bromo-5-chloro-6-fluoro-1H-indazole (10 g, 40.09 mmol, 1 eq) slowly. After the addition the mixture was stirred at 0° C. for 2 hr. TLC (Petroleum ether:Ethyl acetate=3:1) showed all the reactant was consumed and a main new point showed up. Poured the mixture into ice-water, extracted with ethyl acetate (50 mL*3), the combined organic phase was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated to obtain 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole (12 g, crude) as a yellow solid.

Step 2) 4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole

(101) To a solution of 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole (2.34 g, 7.97 mmol, 1 eq) in THF (40 mL) was added 3,4-dihydro-2H-pyran (2.18 ml, 23.9 mmol, 3 eq) and p-toluenesulfonic acid monohydrate (300 mg, 1.59 mmol, 0.2 eq). The reaction mixture was stirred 60° C. for 14 hours. The reaction mixture was extracted with Ethyl Acetate and dried over MgSO.sub.4. The organic residue was purified by column chromatography (silical gel, Hex:Ethyl acetate=1:0 to 4:1). 4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole (1.65 g, 4.35 mmol, 54.7% yield) was obtained.

Step 3) 4-bromo-5-chloro-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-7-amine

(102) To a solution of 4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole (600 mg, 1.58 mmol, 1 eq) in EtOH (5 mL) and H.sub.2O (5 mL) were added NH.sub.4Cl (508.66 mg, 9.51 mmol, 6 eq) and Fe (531.04 mg, 9.51 mmol, 6 eq), then the reaction mixture was stirred at 80° C. for 1 hour. The reaction mixture was filtered, and the filtrate was diluted with ethyl acetate (20 mL), and the mixture was washed with water (20 mL*2), after then the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-TLC (SiO.sub.2, Petroleum ether/Ethyl acetate=1:1). 4-bromo-5-chloro-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-7-amine (390 mg, 1.12 mmol, 70.59% yield) was obtained as a yellow oil.

(103) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.41 (s, 1H), 5.85 (br s, 2H), 5.71 (br d, J=8.0 Hz, 1H), 4.00 (br d, J=11.3 Hz, 1H), 3.77-3.59 (m, 1H), 2.29-2.17 (m, 1H), 2.10-1.91 (m, 2H), 1.78-1.54 (m, 3H).

Intermediate 1D. 4-bromo-5-chloro-6-fluoro-N,N-dimethyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-amine

(104) ##STR00013##

Step 1) 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole

(105) To a solution of Intermediate 1A (900 mg, 3.61 mmol, 1 eq) in H.sub.2SO.sub.4 (10 mL) (98% purity) was added HNO.sub.3 (419.69 mg, 4.33 mmol, 299.78 uL, 1.2 eq) (65% purity) dropwise at −15° C., then the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was slowly poured into ice water (20 mL), then the mixture's pH was adjusted to pH=7 by using saturated aqueous solution of NaOH, after then the mixture was extracted with ethyl acetate (30 mL*2), the combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole (900 mg, crude) was obtained as a yellow solid.

(106) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.36 (br s, 1H), 8.37 (br s, 1H).

Step 2) 4-bromo-5-chloro-6-fluoro-7-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(107) To a solution of 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole (900 mg, 3.06 mmol, 1 eq) (crude) in DCM (10 mL) were added TsOH.H.sub.2O (58.14 mg, 305.64 umol, 0.1 eq) and DHP (771.27 mg, 9.17 mmol, 838.34 uL, 3 eq), then the reaction mixture was stirred at 20° C. for 2 hours. The reaction mixture was diluted with dichloromethane (20 mL), and the mixture was washed with saturated aqueous solution of NaHCO.sub.3 (15 mL*2), the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=40/1 to 25:1, 4-bromo-5-chloro-6-fluoro-7-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole came out at Petroleum ether/Ethyl acetate=40/1, 4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole came out at Petroleum ether/Ethyl acetate=25/1). 4-bromo-5-chloro-6-fluoro-7-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (200 mg, 528.29 umol, 17.28% yield) was obtained as a brown solid. 4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole (600 mg, 1.58 mmol, 51.85% yield) was obtained as a yellow solid.

4-bromo-5-chloro-6-fluoro-7-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(108) .sup.1HNMR (400 MHz, DMSO-d.sub.6) δ 8.43 (s, 1H), 5.50 (dd, J=2.8, 7.8 Hz, 1H), 3.45-3.38 (m, 2H), 2.35-2.27 (m, 1H), 2.23-2.14 (m, 1H), 1.92 (td, J=4.6, 13.6 Hz, 1H), 1.68 (ddt, J=4.0, 10.1, 13.9 Hz, 1H), 1.59-1.36 (m, 2H).

4-bromo-5-chloro-6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-2H-indazole

(109) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.99 (s, 1H), 5.86 (dd, J=2.7, 9.7 Hz, 1H), 4.08-3.96 (m, 1H), 3.81-3.68 (m, 1H), 2.28-2.14 (m, 1H), 2.14-2.02 (m, 1H), 2.02-1.89 (m, 1H), 1.78-1.67 (m, 1H), 1.64-1.56 (m, 2H).

Step 3) 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-amine

(110) To a solution of 4-bromo-5-chloro-6-fluoro-7-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (200 mg, 528.29 umol, 1 eq) in EtOH (5 mL) and H.sub.2O (5 mL) were added NH.sub.4Cl (169.55 mg, 3.17 mmol, 6 eq) and Fe (177.03 mg, 3.17 mmol, 6 eq), then the reaction mixture was stirred at 80° C. for 2 hours. The reaction mixture was filtered, and the filtrate was concentrated to remove EtOH, then the mixture was diluted with ethyl acetate (20 mL), and the mixture was washed with water (20 mL*2), after then the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-amine (140 mg, crude) was obtained as a yellow solid.

Step 4) 4-bromo-5-chloro-6-fluoro-N,N-dimethyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-amine

(111) To a solution of 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-amine (120 mg, 344.24 umol, 1 eq) in THF (5 mL) was added NaH (34.42 mg, 860.59 umol, 60% purity, 2.5 eq) in portions at 0° C. under N.sub.2, then the mixture was stirred at 0° C. for 30 mins under N.sub.2, after then Mel (293.16 mg, 2.06 mmol, 128.58 uL, 6 eq) was added dropwise, and the reaction mixture was stirred at 20° C. for 12 hours under N.sub.2. The reaction mixture was poured into saturated aqueous solution of NH.sub.4Cl (20 mL), then the mixture was extracted with ethyl acetate (20 mL*2), the combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-TLC (SiO.sub.2, Petroleum ether/Ethyl acetate=5:1). Intermediate 1E (30 mg, 78.06 umol, 22.68% yield, 98% purity) was obtained as a yellow oil.

Intermediate 1E. 4-bromo-5-chloro-6-fluoro-N-isopropyl-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-7-amine

(112) ##STR00014##

(113) To a solution of Intermediate 1B (100 mg, 0.218 mmol, 1 eq) in 2-methyl-2-butanol (1.09 mL) was added Xantphos Pd G3 (21 mg, 21.8 μmol, 0.1 eq) and Cs.sub.2CO.sub.3 (142 mg, 0.436 mmol, 2.0 eq). The mixture was degassed and purged with N.sub.2 for 3 times, and then propan-2-amine (0.19 mL, 2.18 mmol, 10 eq) was added. The mixture was stirred at 90° C. for 3 hr in sealed tube. The reaction mixture was diluted with H.sub.2O (40 mL), and then the mixture was extracted with DCM (50 mL*3). The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuum to give a residue. The residue was purified by silica gel chromatography (product came out at Hexane/Ethyl acetate=10/1) to afford Intermediate 1E (47 mg, 0.120 mmol, 55% yield) as beige color solid.

(114) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.43 (s, 1H), 5.74 (dd, J=9.6, 2.5 Hz, 1H), 5.29 (dd, J=9.9, 3.3 Hz, 1H), 4.63-4.57 (m, 1H), 3.99 (d, J=11.0 Hz, 1H), 3.74-3.68 (m, 1H), 2.23-2.17 (m, 1H), 2.05-1.95 (m, 2H), 1.74-1.57 (m, 3H), 1.23-1.18 (m, 6H).

Intermediate 1F. 4-bromo-5-chloro-6-fluoro-N-isopropyl-N-methyl-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-7-amine

(115) ##STR00015##

(116) To a solution of Intermediate 1E (600 mg, 1.54 mmol, 1.0 eq) in Methanol (7.7 mL) was added formaldehyde (0.572 mL, 7.68 mmol, 5.0 eq) and acetic acid (88 μL, 1.54 mmol, 1.0 eq). The mixture was stirred at room temperature for 10 min. Sodium cyanoborohydride (290 mg, 4.61 mmol, 3.0 eq) was added and then the mixture was stirred room temperature for 16 hr. The reaction mixture was quenched by H.sub.2O and extracted with Ethyl acetate (150 mL*3). The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuum to give a residue. The residue was purified by silica gel chromatography (product came out at Hexane/Ethyl acetate=100/4) to afford Intermediate 1F (292 mg, 0.722 mmol, 47% yield) as brown color oil.

(117) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.51 (s, 1H), 5.75 (dd, J=9.3, 2.7 Hz, 1H), 4.14-4.05 (m, 1H), 4.00-3.93 (m, 1H), 3.78-3.67 (m, 1H), 2.92 (d, J=4.4 Hz, 3H), 2.23-2.20 (m, 1H), 2.05-1.95 (m, 2H), 1.75-1.60 (m, 3H), 1.17 (d, J=6.6 Hz, 6H).

Intermediate 1G. 4-bromo-5-chloro-N-ethyl-6-fluoro-N-methyl-1H-indazol-7-amine

(118) ##STR00016##

Step 1) 4-bromo-5-chloro-6-fluoro-1H-indazol-7-amine

(119) To a solution of 4-bromo-5-chloro-6-fluoro-7-nitro-1H-indazole (12 g, 40.75 mmol, 1 eq) in EtOH (100 mL) and H.sub.2O (40 mL) was added Fe (6.83 g, 122.26 mmol, 3 eq) and NH.sub.4Cl (6.54 g, 122.26 mmol, 3 eq). The reaction mixture was heated to 80° C. and reacted for 2 hr. The reaction mixture was filtered through a celite cake, the filtrate was concentrated to give the crude product. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=20/1 to 3/1). 4-bromo-5-chloro-6-fluoro-1H-indazol-7-amine (5 g, 18.90 mmol, 46.39% yield) was obtained as a yellow solid.

Step 2) N-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)acetamide

(120) To a solution 4-bromo-5-chloro-6-fluoro-1H-indazol-7-amine (3 g, 11.34 mmol, 1 eq) in AcOH (30 mL) was added Ac.sub.2O (1.39 g, 13.61 mmol, 1.27 mL, 1.2 eq), the reaction mixture was heated to 80° C. and reacted for 3 hr. The solvent was removed under vacuum. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=50/1 to 4/1) to obtain N-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)acetamide (3 g, 9.79 mmol, 86.29% yield) as a yellow solid.

Step 3) 4-bromo-5-chloro-N-ethyl-6-fluoro-1H-indazol-7-amine

(121) To a solution of LAH (520.00 mg, 13.70 mmol, 1.5 eq) in THF (50 mL) was added a solution of N-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)acetamide (2.8 g, 9.13 mmol, 1 eq) in THF (100 mL) drop-wise under N.sub.2 at 0° C., after the addition, the reaction mixture was allowed to warm to 25° C., and reacted for 16 hr. The mixture was poured into water (500 mL), extracted with ethyl acetate (100 mL*2), the combined organic phase was dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated to give the crude. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=50/1 to 2/1) to obtain 4-bromo-5-chloro-N-ethyl-6-fluoro-1H-indazol-7-amine (1 g, 3.42 mmol, 37.42% yield) as a yellow solid.

Step 4) 4-bromo-5-chloro-N-ethyl-6-fluoro-N-methyl-1H-indazol-7-amine

(122) To a solution of 4-bromo-5-chloro-N-ethyl-6-fluoro-1H-indazol-7-amine (1.4 g, 4.79 mmol, 1 eq) and HCHO (718.48 mg, 23.93 mmol, 659.16 uL, 5 eq) in MeOH (50 mL) was added NaBH3CN (902.21 mg, 14.36 mmol, 3 eq) and AcOH (287.38 mg, 4.79 mmol, 273.70 uL, 1 eq). The reaction mixture was stirred at 25° C. for 16 hr. The solvent was removed under vacuum. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=50/1 to 5/1) to obtain 4-bromo-5-chloro-N-ethyl-6-fluoro-N-methyl-1H-indazol-7-amine (1.4 g, 4.57 mmol, 95.42% yield) as a white solid.

Intermediate 1H. 4-bromo-5-chloro-6-fluoro-7-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(123) ##STR00017##

(124) To a solution of 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.5 g, 1.50 mmol, 1 eq) in THF (10 mL) was added dropwise LDA (2 M, 1.87 mL, 2.5 eq) at −78° C. After addition, the mixture was stirred at this temperature for 2.5 hr, and then Mel (319.12 mg, 2.25 mmol, 139.97 uL, 1.5 eq) was added dropwise at −78° C. The resulting mixture was stirred at 20° C. for 16 hr. The mixture was poured into saturated NH.sub.4Cl and extracted with EA 20 mL. The organic layer was concentrated. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=20/1 to 10/1). We got the desired product 4-bromo-5-chloro-6-fluoro-7-methyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.38 g, 1.09 mmol, 72.93% yield) was obtained as white solid.

Intermediate 1I. 4-bromo-6-fluoro-N,N-dimethyl-5-(methylthio)-1H-indazol-7-amine

(125) ##STR00018##

Step 1) 4-bromo-6-fluoro-7-nitro-1H-indazole

(126) To a solution of 4-bromo-6-fluoro-1H-indazole (10 g, 46.51 mmol, 1 eq) in H.sub.2SO.sub.4 (80 mL) (98% purity) was added KNO.sub.3 (4.70 g, 46.51 mmol, 1 eq) at 0° C. in portions, then the mixture was stirred at 0° C. for 1 h. The reaction mixture was then poured into ice water (200 mL), and the mixture was extracted with ethyl acetate (100 mL*2), the combined organic layers were washed with saturated aqueous solution of NaHCO.sub.3 (100 mL*2) and brine (100 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica gel chromatography (200-300 mesh silica gel, Petroleum ether/Ethyl acetate=15/1 to 1/1, product 4-bromo-6-fluoro-7-nitro-1H-indazole came out at Petroleum ether/Ethyl acetate=8/1) to afford 4-bromo-6-fluoro-7-nitro-1H-indazole (2.7 g, 10.38 mmol, 22.32% yield) as yellow solid and crude product. The cured product was purified by MPLC (Petroleum ether/Ethyl acetate) to afford 4-bromo-6-fluoro-7-nitro-1H-indazole (3.57 g, 13.73 mmol, 29.52% yield) as yellow solid.

Step 2) 4-bromo-6-fluoro-5-iodo-7-nitro-1H-indazole

(127) To a solution of 4-bromo-6-fluoro-7-nitro-1H-indazole (2.7 g, 10.38 mmol, 1 eq) in H.sub.2SO.sub.4 (30 mL) was added NIS (7.01 g, 31.15 mmol, 3 eq) at 25° C. The reaction mixture was stirred at 50° C. for 16 h. The reaction mixture was quenched by ice water (50 mL). Then the mixture was extracted with ethyl acetate (50 mL*3). The combined organic layers were washed with Na.sub.2SO.sub.3 aqueous solution (20 mL*2), NaHCO.sub.3 aqueous solution (20 mL*2) and brine (20 mL), dried over sodium sulfate, filtered and the filtrate was concentrated in vacuum to give 4-bromo-6-fluoro-5-iodo-7-nitro-1H-indazole (3.4 g, 8.81 mmol, 84.85% yield) as yellow solid.

(128) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.28 (br s, 1H), 8.30 (s, 1H).

Step 3) 4-bromo-6-fluoro-5-iodo-1H-indazol-7-amine

(129) To a solution of 4-bromo-6-fluoro-5-iodo-7-nitro-1H-indazole (3.4 g, 8.81 mmol, 1 eq) in EtOH (50 mL) and H.sub.2O (25 mL) was added NH.sub.4Cl (2.83 g, 52.86 mmol, 6 eq), then Fe (2.95 g, 52.86 mmol, 6 eq) was added in portions at 60° C. The mixture was stirred at 80° C. for 1 h. The reaction mixture was filtered through celite while it was still hot. Then the filtrate was concentrated in vacuum to remove EtOH. The resulting aqueous phase was extracted with ethyl acetate (50 mL*2). The combined organic layers were washed with brine (50 mL), dried over sodium sulfate, filtered and the filtrate was concentrated in vacuum to give a residue. The residue was purified by silica gel chromatography (MPLC, Petroleum ether/Ethyl acetate=5/1 to 2/1, product came out at Petroleum ether/Ethyl acetate=2/1) to afford 4-bromo-6-fluoro-5-iodo-1H-indazol-7-amine (2.2 g, 6.18 mmol, 70.16% yield) as gray solid.

(130) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.09 (br s, 1H), 7.86 (d, J=1.7 Hz, 1H), 5.62 (s, 2H).

Step 4) 4-bromo-6-fluoro-5-iodo-N,N-dimethyl-1H-indazol-7-amine

(131) To a solution of 4-bromo-6-fluoro-5-iodo-1H-indazol-7-amine (2.2 g, 6.18 mmol, 1 eq) in MeOH (50 mL) was added AcOH (1.11 g, 18.54 mmol, 1.06 mL, 3 eq), HCHO (5.02 g, 61.81 mmol, 4.60 mL, 10 eq), then NaBH.sub.3CN (3.88 g, 61.81 mmol, 10 eq) was added in portions under 40° C. Gas released and the temperature rise. The suspension was stirred at 25° C. for 16 h. The reaction mixture was poured into water (50 mL), then the mixture was concentrated to remove MeOH, after then the mixture was extracted with ethyl acetate (50 mL*2), and the combined organic layers were washed with brine (50 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure to give a residue. The residue was purified by silica gel chromatography (200-300 mesh silica gel, Petroleum ether/Ethyl acetate=15/1 to 8/1, product came out at Petroleum ether/Ethyl acetate=8/1) to afford 4-bromo-6-fluoro-5-iodo-N,N-dimethyl-1H-indazol-7-amine (2.05 g, 5.34 mmol, 86.37% yield) as off-white solid.

Step 5) 4-bromo-6-fluoro-N,N-dimethyl-5-(methylthio)-1H-indazol-7-amine

(132) To a 100 mL bottle equipped with a magnetic stir bar was added 4-bromo-6-fluoro-5-iodo-N,N-dimethyl-1H-indazol-7-amine (1.2 g, 3.13 mmol, 1 eq), NaSMe (328.56 mg, 4.69 mmol, 1.5 eq), Xantphos (361.65 mg, 625.02 umol, 0.2 eq), K.sub.2CO.sub.3 (1.30 g, 9.38 mmol, 3 eq), dioxane (20 mL) and Pd.sub.2(dba).sub.3 (286.17 mg, 312.51 umol, 0.1 eq) sequentially. The bottle was evacuated and backfilled with nitrogen. Then the mixture was stirred at 90° C. for 16 h under nitrogen atmosphere. The residue was purified by silica gel chromatography (200-300 mesh silica gel, Petroleum ether/Ethyl acetate=20/1 to 8/1, product came out at Petroleum ether/Ethyl acetate=10/1) to afford 4-bromo-6-fluoro-N,N-dimethyl-5-(methylthio)-1H-indazol-7-amine (540 mg, 1.78 mmol, 56.81% yield) as orange solid.

(133) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.59 (br s, 1H), 8.00 (d, J=1.6 Hz, 1H), 2.91 (d, J=2.4 Hz, 6H), 2.39 (s, 3H).

Intermediate 1J. 4-bromo-6-fluoro-N,N-dimethyl-5-(trifluoromethyl)-1H-indazol-7-amine

(134) ##STR00019##

(135) To a solution of 4-bromo-6-fluoro-5-iodo-N,N-dimethyl-1H-indazol-7-amine (1.0 g, 2.61 mmol, 1 eq) and methyl 2,2-difluoro-2-(fluorosulfonyl)acetate (1.00 g, 5.22 mmol, 664.45 uL, 2 eq) in DMF (10 mL) was added CuI (994.63 mg, 5.22 mmol, 2 eq). The mixture was stirred at 100° C. for 6 hr under N.sub.2 atmosphere. The reaction mixture was filtered and the filtrate was diluted with water 50 mL and extracted with Ethyl acetate (50 mL*2). The combined organic layers were washed with brine (50 mL*3), dried over anhydrous Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by silical gel column chromatography (Petroleum ether:Ethyl acetate=1:0 to 10:1). 4-bromo-6-fluoro-N,N-dimethyl-5-(trifluoromethyl)-1H-indazol-7-amine (502 mg, 1.54 mmol, 58.91% yield) was obtained as a yellow solid.

Intermediate 1K. 4-bromo-5-ethyl-6-fluoro-1H-indazole

(136) ##STR00020##

Step 1) 4-bromo-5-ethyl-6-fluoro-2-trityl-2H-indazole

(137) To a solution of diisopropylamine (132.75 mg, 1.31 mmol, 185.41 uL, 1.2 eq) in THF (5 mL) was added slowly n-BuLi (2.5 M, 481.04 uL, 1.1 eq) at −78° C. for 0.5 hr under N.sub.2 atmosphere. Then a solution of 4-bromo-6-fluoro-2-trityl-2H-indazole (500 mg, 1.09 mmol, 1 eq) in THF (2 mL) was added dropwise to the solution. After the mixture was stirred at −78° C. for 0.5 hr, a solution of EtI (204.62 mg, 1.31 mmol, 104.93 uL, 1.2 eq) in THF (2 mL) was added to the mixture and the solution were warmed to 15° C. and stirred for 2 hr under N.sub.2 atmosphere. The reaction mixture was quenched by addition with saturated NH.sub.4Cl aqueous 3 mL at 15° C., was diluted with water 20 mL and extracted with Ethyl acetate (30 mL*2). The combined organic layers were washed with brine (30 mL*2), dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a residue. 4-bromo-5-ethyl-6-fluoro-2-trityl-2H-indazole (500 mg, crude) was obtained as a yellow solid.

Step 2) 4-bromo-5-ethyl-6-fluoro-1H-indazole

(138) To a solution of 4-bromo-5-ethyl-6-fluoro-2-trityl-2H-indazole (500 mg, 1.03 mmol, 1 eq) in DCM (6 mL) was added TFA (3.08 g, 27.01 mmol, 2.00 mL, 26.22 eq). The mixture was stirred at 15° C. for 4 hr. The reaction mixture pH was adjusted to 7 with saturated NaHCO.sub.3 aqueous, and the mixture was extracted with Dichloromethane (30 mL*2). The combined organic layers were washed with brine (30 mL*2), dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex luna C18 150*40 mm*15 um; mobile phase: [water (0.1% TFA)-ACN]; B %: 40%-70%, 10 min). The fraction was concentrated under reduced pressure to remove ACN, the aqueous pH was adjusted to 7 with saturated NaHCO.sub.3 aqueous. The aqueous was extracted with Ethyl acetate (10 mL*2). The combined organic layers were washed with brine (10 mL*2), dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a product. 4-bromo-5-ethyl-6-fluoro-1H-indazole (70 mg, 287.98 umol, 27.96% yield) was obtained as a yellow solid.

(139) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.39 (br s, 1H), 8.01-7.98 (m, 1H), 7.41 (d, J=9.9 Hz, 1H), 2.83 (dq, J=2.4, 7.5 Hz, 2H), 1.14 (t, J=7.5 Hz, 3H).

Intermediate 1L. 4-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine

(140) ##STR00021##

Step 1) 6-fluoro-5-nitro-1H-indazole

(141) To a solution of 6-fluoro-1H-indazole (4.4 g, 32.32 mmol, 1 eq) in H.sub.2SO.sub.4 (30 mL) was added HNO.sub.3 (2.44 g, 38.79 mmol, 1.75 mL, 1.2 eq) dropwise at −15° C., the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was slowly poured into ice water (100 mL), then the mixture was extracted with ethyl acetate (100 mL*2), the combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give 6-fluoro-5-nitro-1H-indazole (5.4 g, crude) was obtained as a yellow solid.

Step 2) 6-fluoro-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(142) To a mixture of 6-fluoro-5-nitro-1H-indazole (4.9 g, 27.05 mmol, 1 eq) (crude) in DCM (50 mL) were added DHP (6.83 g, 81.16 mmol, 7.42 mL, 3 eq) and TsOH.H.sub.2O (514.60 mg, 2.71 mmol, 0.1 eq), and the reaction mixture was stirred at 15° C. for 1 hour. The reaction mixture was poured into saturated solution of NaHCO.sub.3 (100 mL), then the mixture was extracted with dichloromethane (50 mL*2), the combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=20/1 to 15:16-fluoro-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (3 g, 11.31 mmol, 41.81% yield) was obtained as a yellow solid.

(143) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.78 (d, J=7.3 Hz, 1H), 8.41 (s, 1H), 7.97 (d, J=12.1 Hz, 1H), 5.90 (dd, J=2.1, 9.7 Hz, 1H), 3.94-3.85 (m, 1H), 3.82-3.72 (m, 1H), 2.43-2.28 (m, 1H), 2.10-1.93 (m, 2H), 1.82-1.34 (m, 3H).

Step 3) 6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine

(144) To a solution of 6-fluoro-5-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (2.9 g, 10.93 mmol, 1 eq) in MeOH (30 mL) was added wet Pd/C (300 mg, 10% purity) under N.sub.2 atmosphere. The suspension was degassed and purged with H.sub.2 for 3 times. The mixture was stirred under H.sub.2 (15 Psi) at 15° C. for 4 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=15/1 to 8:1). 6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine (1.5 g, 5.87 mmol, 53.65% yield, 92% purity) was obtained as a brick-red solid.

(145) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.82 (s, 1H), 7.43 (d, J=11.6 Hz, 1H), 6.98 (d, J=8.6 Hz, 1H), 5.66 (dd, J=2.3, 9.7 Hz, 1H), 4.91 (s, 2H), 3.85 (br d, J=12.1 Hz, 1H), 3.77-3.62 (m, 1H), 2.42-2.27 (m, 1H), 2.07-1.96 (m, 1H), 1.95-1.86 (m, 1H), 1.76-1.63 (m, 1H), 1.59-1.51 (m, 2H); LCMS (electrospray) m/z 236.1 (M+H)+.

Step 4) 4-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine

(146) To a solution of 6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine (1.45 g, 5.67 mmol, 1 eq) in MeCN (10 mL) was added NBS (1.21 g, 6.80 mmol, 1.2 eq) in portions at 0° C. The mixture was stirred at 0° C. for 2 hours. The reaction mixture was concentrated to give a residue. Then the residue was dissolved in ethyl acetate (30 mL), and the mixture was washed with brine (15 mL*2), the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=20/1). 4-bromo-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-5-amine (1.3 g, 4.14 mmol, 72.98% yield) was obtained as a brown solid.

(147) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.80 (s, 1H), 7.60 (d, J=10.6 Hz, 1H), 5.71 (dd, J=2.5, 9.6 Hz, 1H), 5.15 (s, 2H), 3.88-3.82 (m, 1H), 3.76-3.68 (m, 1H), 2.36-2.27 (m, 1H), 2.02 (br dd, J=4.6, 8.5 Hz, 1H), 1.96-1.90 (m, 1H), 1.76-1.65 (m, 1H), 1.60-1.52 (m, 2H).

Intermediate 1M. 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentan-1-ol

(148) ##STR00022##

Step 1) 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-7-carbaldehyde

(149) To a mixture of Intermediate 1A (3 g, 8.99 mmol, 1 eq) in THF (60 mL) was added LDA (2 M, 17.99 mL, 4 eq) dropwise at −78° C. under N.sub.2. The mixture was stirred at −78° C. for 1 h. After then, HCO.sub.2Et (3.17 g, 35.97 mmol, 3.52 mL, 4 eq) in THF (8 mL) was added dropwise at −78° C., then the mixture was stirred at −78° C. for 2 h. The reaction mixture was quenched by addition of saturated NH.sub.4Cl solution (20 mL) at −78° C., and then extracted with EA (30 mL*3). The combined organic layers were washed with brine (30 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=30/1 to 20/1). 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-7-carbaldehyde (2.78 g, 7.69 mmol, 85.49% yield) was obtained as an off-white solid.

(150) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.40 (s, 1H), 8.35 (s, 1H), 6.09 (dd, J=2.6, 8.9 Hz, 1H), 3.71-3.63 (m, 1H), 3.63-3.52 (m, 1H), 2.42-2.30 (m, 1H), 2.21-2.10 (m, 1H), 2.07-1.95 (m, 1H), 1.77-1.63 (m, 2H), 1.60-1.40 (m, 2H); LCMS (electrospray) m/z 278.9 (M+H)+.

Step 2) 1-(4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-yl)but-3-en-1-ol

(151) To a mixture of 4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-7-carbaldehyde (2.2 g, 6.08 mmol, 1 eq) in THF (60 mL) was added allyl magnesium bromide (1 M, 9.13 mL, 1.5 eq) dropwise at 0° C. under N.sub.2. The mixture was stirred at 0° C. for 2 h. The reaction mixture was quenched by addition of saturated NH.sub.4Cl solution (20 mL) at 0° C., and then extracted with EA (30 mL*3). The combined organic layers were washed with brine (30 mL*2), dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=10/1 to 5/1). 1-(4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-yl)but-3-en-1-ol (2 g, 4.95 mmol, 81.43% yield) was obtained as a colorless oil.

(152) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.25-8.21 (m, 1H), 8.20-8.18 (m, 1H), 6.61 (br d, J=9.0 Hz, 1H), 6.23 (d, J=4.0 Hz, 1H), 6.18 (br d, J=8.3 Hz, 1H), 5.95 (d, J=5.0 Hz, 1H), 5.90-5.75 (m, 2H), 5.36 (dt, J=4.3, 7.5 Hz, 1H), 5.30 (td, J=5.9, 7.9 Hz, 1H), 5.10-4.97 (m, 4H), 3.97 (br d, J=11.5 Hz, 1H), 3.89 (br d, J=11.3 Hz, 1H), 3.69-3.55 (m, 2H), 2.87-2.74 (m, 2H), 2.70-2.55 (m, 4H), 2.06 (br d, J=10.8 Hz, 3H), 1.96-1.87 (m, 1H), 0.90-0.78 (m, 1H); LCMS (electrospray) m/z 302.9 (M+H)+.

Step 3) 4-bromo-7-(3-bromocyclopentyl)-5-chloro-6-fluoro-1H-indazole

(153) To a mixture of 1-(4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-yl)but-3-en-1-ol (2 g, 4.95 mmol, 1 eq) in DCM (20 mL) was added Br.sub.2 (1.19 g, 7.43 mmol, 383.11 uL, 1.5 eq) in DCM (2 mL) dropwise at −20° C. under N.sub.2. The mixture was stirred at −10° C. for 3 h. The mixture was quenched by addition of Na.sub.2SO.sub.3 solution (30 mL), and then diluted with DCM (30 mL). The organic layer was washed with Na.sub.2SO.sub.3 solution (30 mL*2), dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated to obtain a residue. The residue was dissolved in MeOH (15 mL), and then K.sub.2CO.sub.3 (2.05 g, 14.86 mmol, 3 eq) was added and the resulting mixture was stirred at 20° C. for 16 h. The reaction was quenched by addition of water (20 mL), and extracted with EA (30 mL*3), dried by Na.sub.2SO.sub.4, filtered and concentrated to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=10/1 to 3:1). The crude product was purified by reversed-phase HPLC (0.1% FA condition). 4-bromo-7-(3-bromocyclopentyl)-5-chloro-6-fluoro-1H-indazole (300 mg, 752.91 umol, 15.20% yield) was obtained as a white solid.

(154) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44-13.37 (m, 2H), 8.14-8.11 (m, 2H), 5.71-5.67 (m, 1H), 5.44 (dt, J=1.2, 7.5 Hz, 1H), 4.97 (s, 1H), 4.83-4.76 (m, 2H), 4.47 (dd, J=3.7, 10.1 Hz, 1H), 4.22 (dd, J=5.5, 10.1 Hz, 1H), 4.15 (dd, J=2.3, 10.6 Hz, 1H), 3.20-3.13 (m, 1H), 2.69-2.64 (m, 1H), 2.34-2.27 (m, 2H); LCMS (electrospray) m/z 398.8 (M+H)+.

Step 4) 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentyl acetate

(155) To a mixture of 4-bromo-7-(3-bromocyclopentyl)-5-chloro-6-fluoro-1H-indazole (100 mg, 250.97 umol, 1 eq) in DMSO (2 mL) was added KOAc (73.89 mg, 752.91 umol, 3 eq) in one portion at 20° C. under N.sub.2. The mixture was then heated to 70° C. and stirred for 3 h. The reaction was quenched by addition of water (15 mL), and then extracted with EA (20 mL*3), the combined organic layers were washed with brine (20 mL*2), dried by Na.sub.2SO.sub.4, filtered and concentrated to give a residue. 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentyl acetate (100 mg, crude, brown oil) was used directly in the next step without further purification.

(156) LCMS (electrospray) m/z 378.8 (M+H)+.

Step 5) 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentan-1-ol

(157) To a mixture of 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentyl acetate (80 mg, 211.87 umol, 1 eq) in MeOH (4 mL) and H.sub.2O (0.8 mL) was added K.sub.2CO.sub.3 (442.15 mg, 3.20 mmol, 15.1 eq) in one portion at 20° C. under N.sub.2. The mixture was stirred at 20° C. for 2 h. The reaction mixture was quenched by addition of water (15 mL) at 20° C., and then extracted with ethyl acetate (20 mL*3). The combined organic layers were washed with brine (20 mL*1), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=3/1 to 1/2). 3-(4-bromo-5-chloro-6-fluoro-1H-indazol-7-yl)cyclopentan-1-ol (50 mg, 149.01 umol, 70.33% yield) was obtained as a white solid.

(158) LCMS (electrospray) m/z 336.9 (M+H)+.

Intermediate 1N. 4-bromo-6-fluoro-N-isopropyl-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine

(159) ##STR00023##

Step 1) 5-fluoro-2-iodo-4-(trifluoromethyl)aniline

(160) To a solution of 3-fluoro-4-(trifluoromethyl)aniline (4 g, 22.33 mmol, 1 eq) in MeCN (40 mL) was added NIS (5.53 g, 24.57 mmol, 1.1 eq) at 15° C., then reaction mixture was stirred at 15° C. for 15 h. The reaction mixture was diluted with H.sub.2O (100 mL) and extracted with EtOAc (100 mL*3). The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 5-fluoro-2-iodo-4-(trifluoromethyl)aniline (5.6 g, crude) was obtained as a brown oil.

(161) LCMS (electrospray) m/z 305.9 (M+H)+.

Step 2) 5-fluoro-2-methyl-4-(trifluoromethyl)aniline

(162) To a solution of 5-fluoro-2-iodo-4-(trifluoromethyl)aniline (6.0 g, 19.67 mmol, 1 eq) and 2,4,6-trimethyl-1,3,5,2,4,6-trioxatriborinane (8.82 g, 29.51 mmol, 9.82 mL, 42% purity, 1.5 eq) in DME (60 mL) were added Pd(PPh.sub.3).sub.4 (1.14 g, 983.57 umol, 0.05 eq) and K.sub.2CO.sub.3 (8.16 g, 59.01 mmol, 3 eq) at 15° C., then reaction mixture was stirred at 100° C. for 60 h. The reaction mixture was concentrated under reduced pressure to afford the residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=5/1 to 3/1, Petroleum ether/Ethyl acetate=2:1, Rf=0.3). 5-fluoro-2-methyl-4-(trifluoromethyl)aniline (1.6 g, 4.06 mmol, 20.64% yield, 49% purity) was obtained as a yellow oil.

(163) LCMS (electrospray) m/z 194.1.9 (M+H)+.

Step 3) 6-fluoro-5-(trifluoromethyl)-1H-indazole

(164) To a solution of 5-fluoro-2-methyl-4-(trifluoromethyl)aniline (1 g, 5.18 mmol, 1 eq) in AcOH (15 mL) were added NaNO.sub.2 (357.25 mg, 5.18 mmol, 1 eq) and H.sub.2O (3 mL) at 0° C., then the reaction mixture was stirred at 15° C. for 2 h. The reaction was quenched by addition of H.sub.2O (60 mL) at 20° C. and the resulting mixture was extracted with EtOAc (50 mL*3). The combined organic layers were washed with H.sub.2O (50 mL*3), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. Residue was purified by column (SiO2, Petroleum ether/Ethyl acetate=10/1 to 5/1, Petroleum ether/Ethyl acetate=3:1, Rf=0.5). 6-fluoro-5-(trifluoromethyl)-1H-indazole (500 mg, 2.45 mmol, 47.31% yield) was obtained as a yellow solid.

(165) LCMS (electrospray) m/z 205.2 (M+H)+.

Step 4) 6-fluoro-7-nitro-5-(trifluoromethyl)-1H-indazole

(166) To a solution of 6-fluoro-5-(trifluoromethyl)-1H-indazole (500 mg, 2.45 mmol, 1 eq) in H.sub.2SO.sub.4 (5 mL, 95% purity) was added KNO.sub.3 (249 mg, 2.46 mmol, 1.01 eq) at 0° C., then the reaction mixture was stirred at 15° C. for 15 hr. The reaction mixture was diluted with water (100 mL) and extracted with Ethyl acetate (50 mL*2). The combined organic layers were treated with saturated sodium bicarbonate solution until pH=7, dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 6-fluoro-7-nitro-5-(trifluoromethyl)-1H-indazole (500 mg) was obtained as a yellow solid.

(167) LCMS (electrospray) m/z 250.2 (M+H)+.

Step 5) 6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazole

(168) To a solution of 6-fluoro-7-nitro-5-(trifluoromethyl)-1H-indazole (500 mg, 2.01 mmol, 1 eq) in THF (10 mL) was added PPTS (50.44 mg, 200.71 umol, 0.1 eq) and DHP (844.13 mg, 10.04 mmol, 917.53 uL, 5 eq) at 0° C., then the reaction mixture was stirred at 60° C. for 15 hr. The reaction mixture was diluted with solvent H.sub.2O (50 mL) and extracted with EtOAc (50 mL*3). The combined organic layers were washed with H.sub.2O (50 mL*3), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazole (1 g, crude) was obtained as yellow oil.

Step 6) 6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine

(169) To a solution of 6-fluoro-7-nitro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazole (800 mg, 2.40 mmol, 1 eq) and H.sub.2O (2 mL) in EtOH (10 mL) was added NH.sub.4Cl (642.08 mg, 12.00 mmol, 5 eq) and Fe (268.13 mg, 4.80 mmol, 2 eq) at 0° C., then the reaction mixture was stirred at 60° C. for 1 hr. The reaction mixture was diluted with H.sub.2O (20 mL) and extracted with EtOAc (20 mL*3). The combined organic layers were washed with H.sub.2O (30 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=10/1 to 5/1, Petroleum ether:Ethyl acetate=3:1, Rf=0.3). 6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine (500 mg, 1.65 mmol, 68.68% yield) was obtained as a yellow solid

(170) LCMS (electrospray) m/z 220.2 (M+H)+.

Step 7) 4-bromo-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine

(171) To a solution of 6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine (200 mg, 659.51 umol, 1 eq) in DMF (1 mL) was added NBS (129.12 mg, 725.46 umol, 1.1 eq) at 20° C., then the reaction mixture was stirred at 20° C. for 2 hr. The reaction mixture was diluted with H.sub.2O (10 mL) and extracted with EtOAc (10 mL*3). The combined organic layers were washed with H.sub.2O (10 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 4-bromo-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine (120 mg, crude) was obtained as a yellow solid.

(172) LCMS (electrospray) m/z 297.9 (M+H)+.

Step 8) 4-bromo-6-fluoro-N-isopropyl-5-(trifluoromethyl)-1H-indazol-7-amine

(173) To a solution of 4-bromo-6-fluoro-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine (100 mg, 335.53 umol, 1 eq) in MeOH (1 mL) were added AcOH (40.30 mg, 671.06 umol, 38.38 uL, 2 eq) and acetone (97.44 mg, 1.68 mmol, 123.34 uL, 5 eq) at 20° C., NaBH.sub.3CN (105.42 mg, 1.68 mmol, 5 eq) was then added and the reaction mixture was stirred at 20° C. for 2 hr. After then, acetone (97.44 mg, 1.68 mmol, 123.34 uL, 5 eq), NaBH.sub.3CN (105.43 mg, 1.68 mmol, 5 eq) and AcOH (60.45 mg, 1.01 mmol, 57.57 uL, 3 eq) were added to the mixture and the reaction mixture was stirred at 20° C. for 20 hr. The reaction mixture was diluted with H.sub.2O (10 mL) and extracted with EtOAc (10 mL*3). The combined organic layers were washed with H.sub.2O (10 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-TLC (Petroleum ether:Ethyl acetate=3:1, Rf=0.4). 4-bromo-6-fluoro-N-isopropyl-5-(trifluoromethyl)-1H-indazol-7-amine (60 mg, 165.83 umol, 49.42% yield, 94% purity) was obtained as a white solid.

(174) LCMS (electrospray) m/z 340.1 (M+H)+.

Step 9) 4-bromo-6-fluoro-N-isopropyl-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine

(175) To a solution of 4-bromo-6-fluoro-N-isopropyl-5-(trifluoromethyl)-1H-indazol-7-amine (50 mg, 147.01 umol, 1 eq) in THF (1 mL) were added PPTS (3.69 mg, 14.70 umol, 0.1 eq) and DHP (61.83 mg, 735.05 umol, 67.21 uL, 5 eq) at 0° C., then the reaction mixture was stirred at 60° C. for 2 hr. The reaction mixture was diluted with H.sub.2O (50 mL) and extracted with EtOAc (50 mL*3). The combined organic layers were washed with H.sub.2O (50 mL*3), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. Residue was purified by prep-TLC (Petroleum ether:Ethyl acetate=5:1, Rf=0.6). 4-bromo-6-fluoro-N-isopropyl-2-(tetrahydro-2H-pyran-2-yl)-5-(trifluoromethyl)-2H-indazol-7-amine (50 mg, 117.86 umol, 80.17% yield) was obtained as a yellow oil.

(176) LCMS (electrospray) m/z 424.1 (M+H)+.

Intermediate IO. 4-bromo-5-cyclopropyl-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(177) ##STR00024##

Step 1) 3-bromo-5-fluoro-2-methylaniline

(178) To a mixture of 1-bromo-5-fluoro-2-methyl-3-nitrobenzene (23 g, 98.28 mmol, 1 eq) in EtOH (80 mL) and H.sub.2O (80 mL) was added Fe (27.44 g, 491.41 mmol, 5 eq) and NH.sub.4Cl (26.29 g, 491.41 mmol, 5 eq). The mixture was stirred at 100° C. for 3 h. The mixture was filtered and the filtrate was concentrated at reduced pressure to remove EtOH. The resulting mixture was extracted with DCM (50 mL*3). The combined organic phase was washed with brine (50 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure to give a residue to give 3-bromo-5-fluoro-2-methylaniline (20.6 g, crude) as yellow liquid.

(179) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 6.59 (br d, J=8.4 Hz, 1H), 6.42 (br d, J=11.2 Hz, 1H), 5.51 (br s, 2H), 2.09 (s, 3H).

Step 2) 3-bromo-5-fluoro-4-iodo-2-methylaniline

(180) To a mixture of 3-bromo-5-fluoro-2-methylaniline (18 g, 88.22 mmol, 1 eq) (crude) in CH.sub.3CN (150 mL) was added NIS (19.85 g, 88.22 mmol, 1 eq) in portions at 0° C. The mixture was stirred at 30° C. for 3 h. After 3 h, LCMS showed compound 2 was remained and desired mass was detected, too. Then the mixture was stirred at 30° C. for another 12 h. LCMS showed there was no compound 2 remained and one main peak with desired mass was detected. The mixture was quenched with saturated Na.sub.2SO.sub.3 (200 mL) and the resulting mixture was extracted with EtOAc (50 mL*3). The combined organic phase was washed with brine (50 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=50/1, 30/1; TLC (Petroleum ether:Ethyl acetate=10:1; Rf=0.28)) to give 3-bromo-5-fluoro-4-iodo-2-methylaniline (22 g, 66.68 mmol, 75.58% yield) as brown solid.

(181) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 6.55 (d, J=10.5 Hz, 1H), 5.67 (s, 2H), 2.25 (d, J=0.8 Hz, 3H).

Step 3) 4-bromo-6-fluoro-5-iodo-1H-indazole

(182) To a mixture of 3-bromo-5-fluoro-4-iodo-2-methylaniline (22 g, 66.68 mmol, 1 eq) in CH.sub.3COOH (200 mL) was added NaNO.sub.2 (5.52 g, 80.02 mmol, 1.2 eq) which was dissolved water (40 mL) at 0° C. The mixture was stirred at 30° C. for 16 h. The mixture was poured into saturated NaHCO.sub.3 (1000 mL) and the resulting mixture was extracted with EtOAc (200 mL*3). The combined organic phase was washed with brine (100 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=15/1, 5/1) to give 4-bromo-6-fluoro-5-iodo-1H-indazole (7.5 g, 22.00 mmol, 32.99% yield) as brown solid.

(183) .sup.1HNMR (400 MHz, DMSO-d.sub.6) δ 13.58 (br s, 1H), 8.00 (s, 1H), 7.51 (d, J=8.1 Hz, 1H), 3.32 (s, 1H).

Step 4) 4-bromo-6-fluoro-5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(184) To a mixture of 4-bromo-6-fluoro-5-iodo-1H-indazole (7.5 g, 22.00 mmol, 1 eq) and 4-methylbenzenesulfonic acid; hydrate (418.47 mg, 2.20 mmol, 0.1 eq) in DCM (100 mL) was added DHP (5.55 g, 66.00 mmol, 6.03 mL, 3 eq) slowly. The mixture was stirred at 30° C. for 1 h. The mixture was washed with saturated NaHCO.sub.3 (30 mL*3) and brine (30 mL*3). The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=100/1, 50/1) to give 4-bromo-6-fluoro-5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (7.4 g, 17.41 mmol, 79.14% yield) as yellow solid.

(185) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.06 (s, 1H), 7.80 (dd, J=0.7, 8.4 Hz, 1H), 5.83 (dd, J=2.4, 9.6 Hz, 1H), 3.88-3.85 (m, 1H), 3.80-3.70 (m, 2H), 2.40-2.27 (m, 1H), 2.07-1.94 (m, 2H), 1.81-1.63 (m, 2H), 1.62-1.53 (m, 2H).

Step 5) 4-bromo-5-cyclopropyl-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(186) To a mixture of 4-bromo-6-fluoro-5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (1.5 g, 3.53 mmol, 1 eq) and cyclopropylboronic acid (303.14 mg, 3.53 mmol, 1 eq) in dioxane (10 mL) and H.sub.2O (2.5 mL) was added Na.sub.2CO.sub.3 (748.10 mg, 7.06 mmol, 2 eq) and Pd(dppf)Cl.sub.2 (258.23 mg, 352.91 umol, 0.1 eq) under N.sub.2. The mixture was stirred at 80° C. for 16 h. The mixture was concentrated at reduced pressure to give a residue. The residue was purified by prep-TLC (Petroleum ether:Ethyl acetate=20:1) to give 4-bromo-5-cyclopropyl-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.21 g, 619.10 umol, 17.54% yield) as colorless oil.

(187) .sup.1H NMR (400 MHz, CDCl.sub.3) δ 7.98 (d, J=0.6 Hz, 1H), 7.20 (d, J=10.4 Hz, 1H), 5.61 (dd, J=2.8, 9.1 Hz, 1H), 4.03-3.94 (m, 1H), 3.76-3.69 (m, 1H), 2.55-2.42 (m, 1H), 2.19-2.06 (m, 2H), 1.91-1.86 (m, 1H), 1.81-1.64 (m, 3H), 1.12-1.05 (m, 2H), 0.87-0.81 (m, 2H).

Intermediate 1P. 4-bromo-6-fluoro-5-isopropyl-1H-indazole

(188) ##STR00025##

Step 1) 4-bromo-6-fluoro-5-(prop-1-en-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(189) To a mixture of 4-bromo-6-fluoro-5-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (1.5 g, 3.53 mmol, 1 eq) and potassium; trifluoro(isopropenyl)boranuide (626.67 mg, 4.23 mmol, 1.2 eq) in dioxane (10 mL) and H.sub.2O (2 mL) was added Pd(dppf)Cl.sub.2 (258.23 mg, 352.91 umol, 0.1 eq) and Na.sub.2CO.sub.3 (748.10 mg, 7.06 mmol, 2 eq) under N.sub.2. The mixture was stirred at 80° C. for 16 h. The mixture was concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=100/1, 50/1; TLC (Petroleum ether:Ethyl acetate=10:1; Rf=0.61)) to give 0.9 g of yellow oil. This oil was purified by prep-TLC (Petroleum ether:Ethyl acetate=20:1) to give 4-bromo-6-fluoro-5-(prop-1-en-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.55 g, 1.62 mmol, 45.94% yield) as yellow oil.

(190) .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.00 (d, J=0.6 Hz, 1H), 7.28 (d, J=0.9 Hz, 0.5H), 7.26 (d, J=0.7 Hz, 0.5H), 5.64 (dd, J=2.8, 9.0 Hz, 1H), 5.46 (t, J=1.6 Hz, 1H), 5.01 (s, 1H), 4.05-3.97 (m, 1H), 3.80-3.69 (m, 1H), 2.57-2.42 (m, 1H), 2.19-2.09 (m, 2H), 2.07 (s, 3H), 1.81-1.66 (m, 4H).

Step 2) 4-bromo-6-fluoro-5-isopropyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(191) To a solution of 4-bromo-6-fluoro-5-(prop-1-en-2-yl)-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.4 g, 1.18 mmol, 1 eq) in MeOH (10 mL) was added PtO.sub.2 under N.sub.2. The suspension was degassed under vacuum and purged with H.sub.2 several times. The mixture was stirred under H.sub.2 (15 Psi) at 30° C. for 2.5 h. The mixture was filtered and the filtrate was concentrated at reduced pressure to give a residue The residue was purified by silica gel chromatography (300-400 mesh silica gel, Petroleum ether/Ethyl acetate=50/1) to give 4-bromo-6-fluoro-5-isopropyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.3 g, 879.20 umol, 74.56% yield) as colorless oil.

Step 3) 4-bromo-6-fluoro-5-isopropyl-1H-indazole

(192) To a solution of 4-bromo-6-fluoro-5-isopropyl-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole (0.3 g, 879.20 umol, 1 eq) in DCM (1 mL) was added TFA (2.30 g, 20.14 mmol, 1.49 mL, 22.91 eq). The mixture was stirred at 30° C. for 0.5 h. The mixture was concentrated at reduced pressure to give a residue. The residue was diluted with DCM (10 mL) and the resulting mixture was adjusted pH to about 8 with TEA. The mixture was concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (300-400 mesh silica gel, Petroleum ether/Ethyl acetate=30/1, 5/1) to give 4-bromo-6-fluoro-5-isopropyl-1H-indazole (0.2 g, 777.90 umol, 88.48% yield) as colorless oil.

(193) .sup.1H NMR (400 MHz, CDCl.sub.3) δ 8.04 (s, 1H), 7.11 (d, J=11.2 Hz, 1H), 3.75-3.63 (m, 1H), 1.38 (dd, J=1.7, 7.1 Hz, 6H).

Intermediate 1Q. 4-bromo-6-fluoro-5-methoxy-1H-indazole

(194) ##STR00026##

Step 1) 2-bromo-4-fluoro-3-methoxy-1-methylbenzene

(195) To a solution of 2-bromo-6-fluoro-3-methylphenol (4.8 g, 23.41 mmol, 1 eq) in acetone (50 mL) were added K.sub.2CO.sub.3 (6.47 g, 46.82 mmol, 2 eq) and iodomethane (9.97 g, 70.24 mmol, 4.37 mL, 3 eq), and the mixture was stirred at 25° C. for 1 hour. The reaction mixture was concentrated to give a residue. The residue was dissolved in ethyl acetate (50 mL), and the mixture was filtered, and the filtrate was concentrated to give a residue (4.6 g, 21.00 mmol, 89.70% yield) as a yellow oil.

(196) .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 7.05-6.85 (m, 2H), 3.95 (d, J=1.2 Hz, 3H), 2.38 (s, 3H).

Step 2) 3-bromo-1-fluoro-2-methoxy-4-methyl-5-nitrobenzene

(197) To a solution of 2-bromo-4-fluoro-3-methoxy-1-methylbenzene (4.4 g, 20.09 mmol, 1 eq) in H.sub.2SO.sub.4 (40 mL) (98%) was added KNO.sub.3 (2.23 g, 22.10 mmol, 1.1 eq) in portions at 0° C., and the mixture was stirred at 25° C. for 1 hour. The reaction mixture was poured slowly into ice water (200 mL), then the mixture was extracted with ethyl acetate (200 mL*2), the combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 3-bromo-1-fluoro-2-methoxy-4-methyl-5-nitrobenzene (4.6 g, crude) was obtained as a brown oil.

(198) .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 7.70 (d, J=10.9 Hz, 1H), 4.08 (d, J=2.7 Hz, 3H), 2.61 (d, J=1.1 Hz, 3H).

Step 3) 3-bromo-5-fluoro-4-methoxy-2-methylaniline

(199) To a solution of 3-bromo-1-fluoro-2-methoxy-4-methyl-5-nitrobenzene (4.6 g, 17.42 mmol, 1 eq) in EtOH (30 mL) and H.sub.2O (30 mL) were added Fe (5.84 g, 104.53 mmol, 6 eq) and NH.sub.4Cl (5.59 g, 104.53 mmol, 6 eq), and the mixture was stirred at 80° C. for 2 hours. The reaction mixture was filtered, and the filtrate was concentrated to remove EtOH, then the mixture was diluted with EA (50 mL), and the mixture was washed with water (20 mL*2), after then the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. 3-bromo-5-fluoro-4-methoxy-2-methylaniline (3.5 g, crude) was obtained as a brown oil.

(200) .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 6.44 (d, J=11.9 Hz, 1H), 3.83 (s, 3H), 3.76-3.48 (m, 2H), 2.24 (d, J=1.0 Hz, 3H).

Step 4) 4-bromo-6-fluoro-5-methoxy-1H-indazole

(201) To a mixture of 3-bromo-5-fluoro-4-methoxy-2-methylaniline (3.5 g, 14.95 mmol, 1 eq) (crude) in AcOH (20 mL) was added a solution of NaNO.sub.2 (1.24 g, 17.94 mmol, 1.2 eq) in H.sub.2O (4 mL) dropwise at 0° C., then the mixture was stirred at 25° C. for 12 hr. The reaction mixture was diluted with ice water (100 mL), and the mixture was adjusted to pH 7 by using KOH, then the mixture was extracted with EA (100 mL*2), the combined organic layers were washed with brine (50 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/Ethyl acetate=20/1 to 15:1). 4-bromo-6-fluoro-5-methoxy-1H-indazole (600 mg, 2.45 mmol, 16.37% yield) was obtained as a brown solid.

(202) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 8.00 (s, 1H), 7.52 (br d, J=10.4 Hz, 1H), 3.84 (s, 3H).

(203) Synthesis of Formula (I) Compounds

(204) Synthetic methods A to J were used to prepare the compounds of the following. Below, the illustrating synthetic examples of some compounds of the present disclosure are described, and other compounds can be prepared by the similar method to the one described below with different starting or reacting materials.

Synthetic Method A

Example 2. (1S,2S)-2-fluoro-N-(6-(5-methyl-1H-indazol-4-yl)benzo[d]thiazol-2-yl)cyclopropane-1-carboxamide

(205) ##STR00027##

(206) To a solution of Compound 1 (0.2 g, 0.462 mmol, 1 eq) (5-methyl-1H-indazol-4-yl)boronic acid (0.081 g, 0.462 mmol, 1 eq) in dioxane (4 mL) and H.sub.2O (1 mL) was added Na.sub.2CO.sub.3 (0.146 g, 1.38 mmol, 3 eq) and Pd(dppf)Cl.sub.2 (33 mg, 0.046 mmol, 0.1 eq). The mixture was stirred at 110° C. for 16 hr. The reaction mixture was diluted with water (10 mL) and extracted with ethyl acetate (10 mL×2). The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by column chromatography to get Example 2 (135 mg, 0.369 mmol, 80% yield) was obtained as a yellow solid.

(207) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04 (s, NH), 12.76 (s, CONH), 8.05 (s, 1H), 7.86 (d, J=8.0 Hz, 1H), 7.63 (s, 2H), 7.49-7.44 (m, 2H), 7.31 (d, J=8.4 Hz, 1H), 5.05 (td, J12=3.3 Hz, J13=65.7 Hz, 1H), 2.24 (s, 3H), 2.23-2.24 (m, 1H), 1.78-1.73 (m, 1H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 367.1 (M+H)+.

Synthetic Method B

Example 58. (1S,2S)—N-(6-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA

(208) ##STR00028##

Step 1) (1S,2S)—N-(6-(5-chloro-6-fluoro-7-(methylthio)-2-(tetrahydro-2H-pyran-2-yl)-2H-indazol-4-yl)benzo[d]thiazol-2-yl)-2-fluorocyclopropane-1l-carboxamide

(209) To a solution of Compound 3 (4.4 g, 11.59 mmol, 1 eq) in dioxane (100 mL) and H.sub.2O (20 mL) was added Compound 2 (4.20 g, 11.59 mmol, 1 eq), Pd(dppf)Cl.sub.2 (847.97 mg, 1.16 mmol, 0.1 eq) and Na.sub.2CO.sub.3 (2.46 g, 23.18 mmol, 2 eq) under N.sub.2. The reaction mixture was stirred at 90° C. for 12 hr. Water (100 mL) was added and the aqueous phase was extracted with EA (200 mL*2). The combined organic phase was washed with saturated brine (200 mL*2), and concentrated in vacuum. The mixture was purified by column chromatography on silica gel (Petroleum ether:Ethyl acetate=10:1 to 1:1) to give product. Compound 4 (3.9 g, 7.29 mmol, 62.90% yield) as a light yellow solid.

(210) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.00-7.95 (m, 2H), 7.92-7.85 (m, 1H), 7.59 (dd, J=1.8, 8.4 Hz, 1H), 5.70 (dd, J=2.5, 9.5 Hz, 1H), 5.07-4.79 (m, 1H), 3.82-3.63 (m, 1H), 2.72 (d, J=0.9 Hz, 3H), 2.35-2.23 (m, 1H), 2.04-1.94 (m, 2H), 1.81-1.48 (m, 4H), 1.46-1.33 (m, 2H).

Step 2) (1S,2S)—N-(6-(5-chloro-6-fluoro-7-(methylthio)-1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA salt

(211) To a solution of Compound 4 (3.80 g, 7.10 mmol, 1 eq) in DCM (100 mL) was added TFA (9.86 g, 86.51 mmol, 6.41 mL, 12.18 eq) under N.sub.2. The reaction mixture was stirred at 20° C. for 4 hr. DCM (10 ml) was added, Then the MeOH (200 ml) was slowly added. The reaction mixture was stirred at 20° C. for 0.5 hr. The reaction mixture was filtered and the filter cake was concentrated to give product. The filtrate was concentrated in vacuum to give product. Then the crude product was lyophilized to afford Example 58 (3.1 g, 4.26 mmol, 59.98% yield, 2 TFA) as a light yellow solid.

(212) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (br s, 1H), 12.82 (br s, 1H), 8.19 (d, J=1.7 Hz, 1H), 7.96-7.82 (m, 2H), 7.59 (dd, J=1.8, 8.4 Hz, 1H), 5.26-4.85 (m, 1H), 2.57 (s, 3H), 2.30-2.19 (m, 1H), 1.84-1.69 (m, 1H), 1.33 (tdd, J=6.4, 9.0, 12.9 Hz, 1H); LCMS (electrospray) m/z 450.8 (M+H)+.

Synthetic Method C

Example 149. (1S,2S)—N-(5-(5-chloro-7-ethoxy-6-fluoro-1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA

(213) ##STR00029##

Step 1) (1S,2S)-2-fluoro-N-(5-(tributylstannyl)thiazolo[5,4-b]pyridin-2-yl)cyclopropane-1-carboxamide

(214) To a solution of Compound 5 (2.5 g, 7.91 mmol, 1 eq) in dioxane (30 mL) was added (SnBu.sub.3).sub.2 (6.88 g, 11.86 mmol, 5.93 mL, 1.5 eq), Pd(PPh.sub.3).sub.4 (913.78 mg, 790.77 umol, 0.1 eq) and LiCl (1.01 g, 23.72 mmol, 485.85 uL, 3 eq). The mixture was stirred at 110° C. for 16 hr under N.sub.2 atmosphere. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by column chromatography (Silical gel, Petroleum ether:Ethyl acetate=10:1 to 3:1). Compound 6 (1.3 g, 2.47 mmol, 31.24% yield) was obtained as a yellow oil.

Step 2) (1S,2S)—N-(5-(5-chloro-7-ethoxy-6-fluoro-1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA

(215) To a solution of 4-bromo-5-chloro-7-ethoxy-6-fluoro-1H-indazole (100 mg, 264.81 umol, 1 eq) in dioxane (2 mL) were added Compound 6 (167.24 mg, 317.77 umol, 1.2 eq), Pd(PPh.sub.3).sub.4 (30.60 mg, 26.48 umol, 0.1 eq) and LiCl (33.68 mg, 794.42 umol, 16.27 uL, 3 eq). The mixture was stirred at 140° C. for 2 hr under microwave. After then, the reaction mixture was added with saturated K.sub.2CO.sub.3 aqueous 10 mL and stirred at 20° C. for 15 min. The mixture was diluted with water 10 mL and extracted with Ethyl acetate (20 mL*2). The combined organic layers were washed with brine (20 mL*2), dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by prep-TLC (Silical gel plate, Petroleum ether:Ethyl acetate=1:2) to give a crude product. The crude product was purified by prep-HPLC (column: Phenomenex luna C18 150*25 mm*10 um; mobile phase: [water (0.1% TFA)-ACN]; B %: 55%-85%, 10 min). Example 149 (60 mg, 112.36 umol, 42.43% yield) was obtained as a yellow oil.

(216) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.97 (s, 1H), 8.28 (d, J=8.4 Hz, 1H), 7.95 (s, 1H), 7.81 (d, J=8.4 Hz, 1H), 6.12-6.06 (m, 1H), 5.20-4.96 (m, 1H), 4.46-4.34 (q, J=7.0 Hz, 2H), 3.97 (m, 1H), 3.73-3.61 (m, 1H), 2.47-2.40 (m, 1H), 2.32-2.22 (m, 1H), 2.04 (m, 2H), 1.83-1.69 (m, 2H), 1.57 (m, 2H), 1.49 (t, J=7.0 Hz, 3H), 1.41-1.28 (m, 1H).

Synthetic Method D

Example 152. (1S,2S)—N-(5-(5-ethyl-6-fluoro-1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(217) ##STR00030##

(218) To a solution of Intermediate 1K (45 mg, 185.13 umol, 1 eq) in EtOH (2 mL) were added Compound 6 (116.92 mg, 222.15 umol, 1.2 eq) and Ad.sub.2nBuP-Pd-G3 (13.48 mg, 18.51 umol, 0.1 eq). The mixture was stirred at 80° C. for 16 hr under N.sub.2 atmosphere. The reaction mixture was diluted with water 20 mL and extracted with Ethyl acetate (20 mL*2). The combined organic layers were washed with brine (20 mL*2), dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex luna C18 150*25 mm*10 um; mobile phase: [water (0.1% TFA)-ACN]; B %: 33%-63%, 10 min) to give a crude product. The crude product was purified by prep-TLC (Silical gel plate, Petroleum ether:Ethyl acetate=1:1). Example 152 (9.7 mg, 24.29 umol, 13.12% yield, 100% purity) was obtained as a white solid.

(219) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (br s, 1H), 12.94 (br s, 1H), 8.26 (d, J=8.2 Hz, 1H), 7.72 (s, 1H), 7.68 (d, J=8.3 Hz, 1H), 7.42 (d, J=10.1 Hz, 1H), 5.20-4.95 (m, 1H), 2.65 (dq, J=2.4, 7.2 Hz, 2H), 2.27 (m, 1H), 1.85-1.69 (m, 1H), 1.34 (m, 1H), 1.11 (t, J=7.0 Hz, 3H); LCMS (electrospray) m/z 400.4 (M+H)+.

Synthetic Method E

Example 221. (1S,2S)-2-fluoro-N-(6-(5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

(220) ##STR00031##

Step 1) (1S,2S)-2-fluoro-N-(6-iodoimidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

(221) A mixture of Compound 7 (5.890 g, 22.737 mmol), (1S,2S)-2-fluorocyclopropane-1-carboxylic acid (3.076 g, 29.558 mmol) and 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (EDC-HCl, 6.538 g, 34.105 mmol) in dichloromethane (100 mL) was treated at the room temperature with N,N-diisopropylethylamine (2.376 mL, 13.642 mmol), stirred at the same temperature for 40 hr. The precipitates were collected by filtration, washed by dichloromethane, and dried to give Compound 8 as beige solid (3.870 g, 49.3%).

(222) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.99 (s, 1H), 8.87 (s, 1H), 8.02 (s, 1H), 7.36˜7.23 (m, 2H), 4.97˜4.77 (m, 1H), 2.09˜2.07 (m, 1H), 1.65˜1.57 (m, 1H), 1.16˜1.09 (m, 1H).

Step 2) (1S,2S)-2-fluoro-N-(6-(5-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide

(223) Compound 8 (0.750 g, 2.173 mmol), (5-methyl-1H-indazol-4-yl)boronic acid (0.459 g, 2.608 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl.sub.2, 0.159 g, 0.217 mmol) and cesium carbonate (1.416 g, 4.346 mmol) in tetrahydrofuran (15 mL)/water (4 mL) was mixed at the room temperature and then heated at 120° C. under the microwaves for 1 hr, cooled down to the room temperature, filtered through a celite pad to remove solids, and partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried (anhydrous MgSO4), filtered, and concentrated in vacuo. The residue was chromatographed (SiO.sub.2, 30 g cartridge; ethyl acetate/hexane=100%) to give the crude product which was crystallized at the room temperature using diethylether (5 mL). The resulting precipitates were filtered, washed by diethylether, and dried to give Example 221 as light yellow solid (0.550 g, 72.4%).

(224) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.77 (s, 1H), 9.70 (s, 1H), 9.00 (s, 1H), 8.66 (d, J=9.2 Hz, 1H), 8.59 (s, 1H), 8.55 (d, J=9.2 Hz, 1H), 8.33 (d, J=8.0 Hz, 1H), 8.14 (d, J=8.8 Hz, 1H), 5.91˜5.71 (m, 1H), 3.11 (s, 3H), 3.05˜3.00 (m, 1H), 2.54˜2.48 (m, 1H), 2.07˜2.03 (m, 1H); LCMS (electrospray) m/z 350.0 (M+H)+.

Synthetic Method F

Example 223. N-(6-(5-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide. dihydrochloride

(225) ##STR00032##

Step 1) (2-amino-6-iodoimidazo[1,2-a]pyridin-3-yl)(cyclopropyl)methanone

(226) To a solution of cyclopropanecarboxylic acid (3.17 g, 36.78 mmol, 2.91 mL, 1.3 eq) in DCM (50 mL) was added EDCI (6.51 g, 33.95 mmol, 1.2 eq), HOBt (4.59 g, 33.95 mmol, 1.2 eq) and TEA (8.59 g, 84.89 mmol, 11.82 mL, 3 eq). The mixture was stirred at 20° C. for 1 hr. then added Compound 7 (6 g, 28.30 mmol, 1 eq). The final mixture was stirred at 20° C. for 18 hr. The mixture was poured into H.sub.2O (200 mL) and extracted with Ethyl acetate (300 mL*3), the organic phase was washed with brine (500 mL*2) and dried with anhydrous sodium sulfate (Na.sub.2SO.sub.4), filtered and concentrated in vacuum. The residue was purified by trituration with Ethyl acetate (50 mL), filtered and the filter cake was concentrated. Compound 9 (1.9 g, 6.78 mmol, 23.96% yield) was obtained as yellow solid.

(227) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 9.70 (d, J=1.2 Hz, 1H), 7.60 (dd, J=2.1, 9.3 Hz, 1H), 7.32 (d, J=9.3 Hz, 1H), 6.62 (s, 2H), 2.46-2.37 (m, 1H), 1.02-0.90 (m, 4H).

Step 2) (1S,2S)-2-fluoro-N-(6-(5-methyl-1H-indol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropane-1-carboxamide dihydrochloride

(228) To a solution of Compound 9 (10.22 g, 31.27 mmol, 1 eq) and 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (11.12 g, 43.78 mmol, 1.4 eq) in dioxane (100 mL) was added KOAc (9.21 g, 93.82 mmol, 3 eq) and Pd(dppf)Cl.sub.2 (1.14 g, 1.56 mmol, 0.05 eq). The mixture was heated to 90° C. for 3 hr. The residue was poured into water (200 mL). The aqueous phase was extracted with ethyl acetate (200 mL*2). The combined organic phase was washed with brine (300 mL), dried with anhydrous Na.sub.2SO.sub.4, filtered and concentrated in vacuum. TLC (Petroleum ether/Ethyl acetate=0:1) showed a main spot. The residue was purified by silica gel chromatography eluted with Petroleum ether/Ethyl acetate=0:1. Compound 10 (11 g, crude) was obtained as yellow solid. The crude was purified by triturated with Petroleum ether (20 mL) and Ethyl acetate (4 mL), filtered and the filter cake was concentrated. Compound 10 (6.3 g, 19.26 mmol, 48.46% yield) was obtained as white solid.

Step 3) N-(6-(5-chloro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide. Dihydrochloride

(229) To a solution of Compound 10 (100 mg, 305.64 umol, 1 eq) and 4-bromo-5-chloro-1H-indazole (84.90 mg, 366.76 umol, 1.2 eq) in dioxane (3 mL) and H.sub.2O (1 mL) was added Na.sub.2CO.sub.3 (97.18 mg, 916.91 umol, 3 eq) and Pd(dppf)Cl.sub.2 (11.18 mg, 15.28 umol, 0.05 eq). The mixture was stirred at 90° C. for 10 hr. The mixture was poured into Petroleum ether (10 mL), filtered with silica gel and the filtrate was concentrated in vacuum. The residue was purified by prep-HPLC (column: Phenomenex Synergi C18 150*25*10 um; mobile phase: [water (0.05% HCl)-ACN]; B %: 14%-34%, 9 min), followed by lyophilization. Example 223 (36.8 mg, 85.95 umol, 28.12% yield, 99.2% purity, 2 HCl) was obtained as white solid.

(230) .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.92 (s, 1H), 8.13 (s, 1H), 7.99-7.91 (m, 3H), 7.68 (dd, J=1.0, 8.9 Hz, 1H), 7.58 (d, J=8.9 Hz, 1H), 1.95-1.87 (m, 1H), 1.12-1.07 (m, 2H), 1.05-0.98 (m, 2H); LCMS (electrospray) m/z 352.0 (M+H)+.

Synthetic Method G

Example 231. N-(6-(5-bromo-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide. 2 TFA salt

(231) ##STR00033##

(232) A mixture of CuBr (137.29 mg, 957.04 umol, 29.15 uL, 1 eq) and t-BuONO (98.69 mg, 957.04 umol, 113.83 uL, 1 eq) in MeCN (5 mL) was stirred at 0° C. for 30 mins, after then a solution of Example 227 (662 mg, 957.04 umol, 1 eq) in MeCN (1 mL) was added, and the mixture was stirred at 20° C. for 2 hours, after then CuBr (137.29 mg, 957.04 umol, 29.15 uL, 1 eq) and t-BuONO (98.69 mg, 957.04 umol, 113.83 uL, 1 eq) were added, and the mixture was stirred at 20° C. for another 12 hours. The reaction mixture was concentrated to give a residue, then the residue was dissolved in ethyl acetate (50 mL), after then the mixture was washed with diluted ammonium hydroxide (3%, 20 mL*2), the organic layer was washed with brine (20 mL), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex Synergi C18 150*25*10 um; mobile phase: [water (0.1% TFA)-ACN]; B %: 20%-50%, 9 min). Example 231 (14 mg, 22.01 umol, 2.3% yield, 2TFA) was obtained as a yellow solid.

(233) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.05 (s, 1H), 8.78 (s, 1H), 8.14 (s, 1H), 7.92 (s, 1H), 7.64 (d, J=8.7 Hz, 1H), 7.57 (d, J=9.2 Hz, 1H), 7.32 (dd, J=1.7, 9.2 Hz, 1H), 2.05-1.86 (m, 1H), 0.85-0.79 (m, 4H); LCMS (electrospray) m/z 414.1 (M+H)+.

Synthetic Method H

Example 258. (1S,2S)—N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(234) ##STR00034##

Step 1) (1S,2S)—N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(235) To a solution of Intermediate 1D (30 mg, 78.06 umol, 1 eq) and Compound 11 (32.33 mg, 93.67 umol, 1.2 eq) in dioxane (1 mL) and H.sub.2O (0.2 mL) were added Pd(dppf)Cl.sub.2 (5.71 mg, 7.81 umol, 0.1 eq) and Na.sub.2CO.sub.3 (24.82 mg, 234.17 umol, 3 eq), then the mixture was stirred at 80° C. for 12 hours under N.sub.2. The reaction mixture was concentrated to give a residue. The residue was purified by prep-TLC (SiO.sub.2, Dichloromethane:Methanol=10:1). Compound 12 (34 mg, 57.44 umol, 73.59% yield, 87% purity) was obtained as a yellow oil.

Step 2) (1S,2S)—N-(6-(5-chloro-7-(dimethylamino)-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(236) To a solution of Compound 12 (34 mg, 57.44 umol, 1 eq) in dioxane (1 mL) was added HCl/dioxane (4 M, 1 mL, 69.64 eq), then the mixture was stirred at 20° C. for 2 hours under N.sub.2. The reaction mixture was diluted with ethyl acetate (20 mL), and the mixture was washed with saturated aqueous solution of NaHCO.sub.3 (15 mL*2), the organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to give a residue. The residue was purified by prep-HPLC (column: Phenomenex luna C.sub.18 150*25 10u; mobile phase: [water (0.1% TFA)-ACN]; B %: 23%-53%, 10 min). Example 258 (8.7 mg, 13.05 umol, 22.72% yield, 2 TFA) was obtained as a white solid.

(237) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (br s, 1H), 11.21 (s, 1H), 8.80 (s, 1H), 8.17 (s, 1H), 7.95 (s, 1H), 7.62 (d, J=9.2 Hz, 1H), 7.43 (d, J=9.2 Hz, 1H), 5.08-4.77 (m, 1H), 3.01 (s, 3H), 3.00 (s, 3H), 2.16 (td, J=7.0, 13.8 Hz, 1H), 1.76-1.57 (m, 1H), 1.27-1.11 (m, 1H); LCMS (electrospray) m/z 431.2 (M+H)+.

Synthetic Method I

Example 393. (1S,2S)—N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(238) ##STR00035##

Step 1) 1-(4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-yl)ethan-1-one

(239) To a solution of Intermediate 1A (3.29 g, 9.86 mmol, 1 eq) in THF (49 mL) was cooled to −78° C. then, LDA (7.39 mL, 14.7 mmol, 1.5 eq) was added slowly to reaction mixture, stirred at the same temperature for 30 min. Then acetic anhydride (1.11 mL, 11.8 mmol, 1.2 eq) was added dropwise and the reaction mixture was stirred at rt for 2 hrs. After the Intermediate 1A was consumed, quenched with water and extracted with DCM, separated, dried over anhydrous MgSO.sub.4, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (product came out at Hexane/Ethyl acetate=10/1) to afford Compound 13 (1.86 g, 4.95 mmol, 50.2% yield) as an orange solid.

Step 2) 1-(4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-7-yl)ethan-1-ol

(240) To a solution of Compound 13 (1.86 mg, 4.95 mmol, 1 eq) in MeOH (24 mL) were cooled to 0° C. then sodium borohydride (375 mg, 9.90 mmol, 2 eq) was added portionwise. The reaction mixture was stirred at rt for 2 hrs. After the Compound 13 was consumed, the reaction mixture was concentrated and extracted with DCM, washed with water, separated, dried over anhydrous MgSO.sub.4, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography (product came out at Hexane/Ethyl acetate=7/3) to afford Compound 14 (615 mg, 1.62 mmol, 32% yield) as an ivory solid.

Step 3) 7-(1-(2H-tetrazol-2-yl)ethyl)-4-bromo-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole

(241) To a solution of Compound 14 (100 mg, 0.265 mmol, 1.0 eq) in THF (1.33 mL) was added 1H-tetrazole (0.89 mL, 0.398 mmol, 1.5 eq) and PPh.sub.3 (104 mg, 0.398 mmol, 1.5 eq). The mixture was cooled to 0° C. and DEAD (0.181 mL, 0.398 mmol, 1.5 eq) was added slowly at 0° C. The mixture was stirred at room temperature for 1 hr. The reaction mixture was extracted with DCM (30 mL*3). The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuum. The crude product was purified by silica gel chromatography (product came out Hexane/Ethyl acetate=10/2) to afford Compound 15 (62 mg, 0.144 mmol, 54% yield) as a white color solid.

Step 4) (1S,2S)—N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1-(tetrahydro-2H-pyran-2-yl)-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(242) To a solution of Compound 15 (62 mg, 0.144 mmol, 1 eq) in 1,4-Dioxane (0.577 mL)/H.sub.2O (0.144 mL) were added Compound 11 (54 mg, 0.159 mmol, 1.1 eq), Pd(dppf)Cl.sub.2 (5 mg, 0.007 mmol, 0.05 eq), Na.sub.2CO.sub.3 (30 mg, 0.289 mmol, 2 eq). The mixture was degassed and purged with N.sub.2 for 3 times. The mixture was stirred at 120° C. for 30 min in microwave reactor. The reaction mixture was filtered through celite and filtrate was extracted with DCM. The combined organic layers were dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuum to give a residue. The residue was purified by silica gel chromatography (product came out at Hexane/Ethyl acetate=2/8) to afford Compound 16 (68 mg, 0.120 mmol, 83%) as a yellow solid.

Step 5) (1S,2S)—N-(6-(7-(1-(2H-tetrazol-2-yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(243) To a solution of Compound 16 (66 mg, 0.116 mmol, 1 eq) in Ethyl acetate (0.6 mL) was added 1 N HCl in EA solution (1.16 mL, 1.16 mmol, 10 eq). The mixture was stirred at room temperature for 1 hr. The reaction mixture was quenched by saturated NaHCO.sub.3 and extracted with EA, dried over Na.sub.2SO.sub.4, filtered and the filtrate was concentrated in vacuum. The crude product was purified by silica gel chromatography (product came out at DCM/MeOH=10/1) to afford Example 393 (4 mg, 0.008 mmol, 7%) as an ivory solid.

(244) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.77 (s, 1H), 11.07 (s, 1H), 8.99 (s, 1H), 8.80 (s, 1H), 8.14-8.04 (m, 2H), 7.58-7.54 (m, 1H), 7.35 (dd, J=9.3, 1.6 Hz, 1H), 6.74 (q, J=7.1 Hz, 1H), 5.00-4.79 (m, 1H), 2.23 (d, J=7.2 Hz, 3H), 2.16-2.09 (m, 1H), 1.68-1.57 (m, 1H), 1.18-1.09 (m, 1H)); LCMS (electrospray) m/z 485.10 (M+H)+.

Synthetic Method J

Example 446. (1S,2S)-2-fluoro-N-(5-(5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide

(245) ##STR00036##

Step 1) (1S,2S)—N-(5-bromopyrazolo[1,5-a]pyridin-2-yl)-2-fluorocyclopropane-1-carboxamide

(246) To a mixture of Compound 17 (3.1 g, 14.62 mmol, 1 eq) and (1S,2S)-2-fluorocyclopropanecarboxylic acid (1.67 g, 16.08 mmol, 1.1 eq) in CH.sub.3CN (40 mL) was added MsCl (3.35 g, 29.24 mmol, 2.26 mL, 2 eq) and 3-methylpyridine (6.81 g, 73.10 mmol, 7.12 mL, 5 eq) slowly at 0° C. under N.sub.2. The mixture was stirred at 30° C. for 3 h. The mixture was concentrated at reduced pressure. The residue was dissolved with ethyl acetate (200 mL) and the resulting mixture was washed with 10% citric acid (30 mL*2), saturated Na.sub.2CO.sub.3 (30 mL*2), brine (30 mL*2), dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=5/1, 3/1) to give Compound 18 (2.3 g, 7.72 mmol, 52.81% yield) as white solid.

Step 2) (1S,2S)-2-fluoro-N-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropane-1-carboxamide

(247) Compound 18 (0.345 g, 1.159 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane, 0.588 g, 2.318 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (Pd(dppf)Cl.sub.2, 0.084 g, 0.115 mmol) and potassium acetate (0.398 g, 4.056 mmol) were mixed at the room temperature in DMSO (10 mL) and then stirred at 90° C. for 18 h, cooled down to the room temperature, filtered through a celite pad to remove solids, and partitioned between ethyl acetate and water. The organic layer was washed with aqueous saturated sodium chloride solution, separated, dried with anhydrous MgSO.sub.4, filtered, and concentrated in vacuo. The residue was chromatographed (SiO.sub.2, 12 g cartridge; ethyl acetate/hexane=0% to 100%) to give Compound 19 as brown solid (0.289 g, 72.3%).

Step 3) (1S,2S)-2-fluoro-N-(5-(5-methyl-1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)cyclopropanecarboxamide

(248) To a mixture of Compound 19 (6 g*, 17.34 mmol, 1 eq) and 4-bromo-5-methyl-1H-indazole (3.6 g, 17.34 mmol, 1 eq) in dioxane (120 mL) and H.sub.2O (24 mL) was added Na.sub.2CO.sub.3 (3.67 g, 34.68 mmol, 2 eq) and Pd(dppf)Cl.sub.2 (1.28 g, 1.73 mmol, 0.1 eq) under N.sub.2. The mixture was stirred at 90° C. for 4 h. The mixture was concentrated at reduced pressure to give a residue. The residue was purified by silica gel chromatography (1000 mesh silica gel, Petroleum ether/Ethyl acetate=5/1, 1/1; TLC (Petroleum ether:Ethyl acetate=1:1; Rf=0.08) to give 2.5 g of yellow solid. This solid was triturated with CH.sub.3CN (10 mL) for two times. The mixture was filtered and the filtered cake was collected. The cake was dispersed with H.sub.2O/CH.sub.3CN (5:1; 10 mL) and the resulting mixture was lyophilizated for third times to give Example 446 (1.53 g, 4.37 mmol, 25.20% yield, 96.98% purity) as pale solid.

(249) .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.09 (s, 1H), 11.13 (s, 1H), 8.61 (d, J=7.1 Hz, 1H), 7.74 (s, 1H), 7.63 (d, J=0.9 Hz, 1H), 7.49 (d, J=8.6 Hz, 1H), 7.32 (d, J=8.6 Hz, 1H), 6.91 (s, 1H), 6.86 (dd, J=1.9, 7.0 Hz, 1H), 5.06-4.98 (m, 1H), 4.88-4.84 (m, 1H), 2.34 (s, 3H), 2.15 (td, J=6.9, 13.8 Hz, 1H), 1.74-1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 350.1 (M+H)+.

(250) Table 1 below shows the compounds of Examples along with general synthetic methods used to make the compound and characterization data.

(251) TABLE-US-00001 TABLE 1 Compounds of Examples Meth- Ex # Structure/Name .sup.1H NMR/MS (M + 1) od 1 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04 (s, NH), 12.69 (s, CONH), 8.03 (s, 1H), 7.84 (d, J = 8.4 Hz, 1H), 7.63 (s, 1H), 7.48-7.44 (m, 1H), 7.31 (d, J = 8.4 Hz, 1H), 2.30 (s, 3H), 2.02 (t, J = 5.6 Hz, 1H), 0.97 (t, J = 4.0 Hz, 4H); LCMS (electrospray) m/z 349.0 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 2 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04 (s, NH), 12.76 (s, CONH), 8.05 (s, 1H), 7.86 (d, J = 8.0 Hz, 1H), 7.63 (s, 2H), 7.49-7.44 (m, 2H), 7.31 (d, J = 8.4 Hz, 1H), 5.05 (td, J12 = 3.3 Hz, J13 = 65.7 Hz, 1H), 2.24 (s, 3H), 2.23-2.24 (m, 1H), 1.78-1.73 (m, 1H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 367.1 (M + H)+. A (1S,2S)-2-fluoro-N-(6-(5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 3 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.03 (s, 1H), 11.80 (s, 1H), 7.99 (s, 1H), 7.78 (d, 8.4 Hz, 1H), 7.63 (s, 1H), 7.46-7.42 (m, 2H), 7.31 (d, 8.4 Hz, 1H), 2.30 (s, 3H), 1.52 (s, 9H); LCMS (electrospray) m/z 381.1 (M + H)+. A tert-butyl (6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)carbamate 4 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.02 (br s, 1H), 12.28 (br s, 1H), 8.04 (d, J = 1.3 Hz, 1H), 7.83 (d, J = 8.3 Hz, 1H), 7.63 (s, 1H), 7.50-7.43 (m, 2H), 7.31 (d, J = 8.4 Hz, 1H), 3.44 (quin, J = 8.5 Hz, 1H), 2.32-2.13 (m, 7H), 2.06-1.92 (m, 1H), 1.90-1.78 (m, 1H); LCMS (electrospray) m/z 363.2 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclobutanecarboxamide. 2 TFA 5 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.21-12.83 (m, 2H), 8.08 (d, J = 1.2 Hz, 1H), 7.89 (d, J = 8.3 Hz, 1H), 7.64 (s, 1H), 7.52-7.43 (m, 2H), 7.32 (d, J = 8.6 Hz, 1H), 3.02 (td, J = 9.5, 13.0 Hz, 1H), 2.30 (s, 3H), 2.23-2.11 (m, 2H); LCMS (electrospray) m/z 385.0 (M + H)+. A 2,2-difluoro-N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 2 TFA salt 6 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.05 (br s, 1H), 12.50 (s, 1H), 8.06 (d, J = 1.3 Hz, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.63 (s, 1H), 7.50-7.44 (m, 2H), 7.32 (d, J = 8.6 Hz, 1H), 5.19-4.95 (m, 1H), 2.97- 2.85 (m, 1H), 2.66-2.57 (m, 2H), 2.45-2.35 (m, 2H), 2.30 (s, 3H); LCMS (electrospray) m/z 381.1 (M + H)+. A (1S,3S)-3-fluoro-N-(6-(5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2- yl)cyclobutane-1-carboxamide. 2 TFA 7 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.03 (br s, 1H), 12.48 (s, 1H), 8.06 (d, J = 1.3 Hz, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.63 (s, 1H), 7.50-7.43 (m, 2H), 7.32 (d, J = 8.6 Hz, 1H), 5.37-5.15 (m, 1H), 3.45 (br d, J = 3.1 Hz, 1H), 2.65-2.55 (m, 2H), 2.45-2.35 (m, 2H), 2.30 (s, 3H); LCMS (electrospray) m/z 381.1 (M + H)+. A (1R,3R)-3-fluoro-N-(6-(5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2- yl)cyclobutane-1-carboxamide. 2 TFA 8 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04(s, 1H), 12.93(s, 1H), 8.16(dd, J = 8.4 Hz, J = 2.0 Hz, 2H), 8.10(s, 1H), 7.91(d, J = 7.6 Hz, 1H), 7.70-7.65(m, 2H), 7.60-7.57(m, 2H), 7.53(dd, J = 8.4 Hz, 2.0 Hz, 1H), 7.47(d, J = 8.4 Hz, 1H), 7.32(d, J = 8.8 Hz, 1H), 2.32(s, 3H); LCMS (electrospray) m/z 385.1 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)benzamide 9 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.99 (s, NH), 12.31 (s, NH), 7.99 (s, 1H), 7.80 (d, J = 8.0 Hz, 1H), 7.58 (s, 1H), 7.44-7.40 (m, 2H), 7.27 (d, J = 8.0 Hz, 1H), 2.26 (s, 3H), 1.59 (m, 2H), 1.31-1.29 (m, 2H), 0.89-0.85 (m, 3H); LCMS (electrospray) m/z 365.1 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)pentanamide 10 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.98 (s, NH), 12.32 (s, NH), 7.99 (s, 1H), 7.80 (d, J = 8.0 Hz, 1H), 7.58 (s, 1H), 7.44-7.40 (m, 2H), 7.27 (d, J = 8.0 Hz, 1H), 2.96 (m, 1H), 2.26 (s, 3H), 1.89 (m, 2H), 1.79-1.49 (m, 4H), 1.24-1.20 (m, 1H), 0.83- 0.80 (m, 1H); LCMS (electrospray) m/z 377.1 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopentanecarboxamide 11 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.08 (br s, 1H), 12.60 (br s, 1H), 8.07 (d, J = 1.3 Hz, 1H), 7.86 (d, J = 8.2 Hz, 1H), 7.64 (s, 1H), 7.51-7.43 (m, 2H), 7.32 (d, J = 8.6 Hz, 1H), 3.38-3.25 (m, 1H), 2.98- 2.81 (m, 4H), 2.30 (s, 3H); LCMS (electrospray) m/z 377.1 (M + H)+. A 3,3-difluoro-N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclobutane-1- carboxamide. 2 TFA 12 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) d 13.00 (s, 1H), 12.17 (s, 1H), 8.82 (d, J = 4.4 Hz, 1H), 8.24 (d, J = 8.0 Hz, 1H), 8.16-8.12 (m, 2H), 7.93 (d, J = 8.8 Hz, 1H), 7.76 (dd, J = 7.2, 4.8 Hz, 1H), 7.64 (s, 1H), 7.52 (dd, J = 8.4, 1.6 Hz, 1H), 7.47 (d, J = 8.4 Hz, 1H), 7.32 (d, J = 8.4 Hz, 1H), 2.32 (s, 3H); LCMS (electrospray) m/z 386.1 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)picolinamide 13 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31(s, 1H), 12.74(brs, 1H), 8.43(s, 1H), 7.93(d, J = 1.6 Hz, 1H), 7.73(d, J = 2.4 Hz, 1H), 7.71(s, 1H), 7.60(d, J = 3.2 Hz, 2H), 7.36-7.34(m, 1H), 7.31(dd, J = 8.4 Hz, J = 1.2 Hz, 1H), 6.92-6.89(m, 1H), 6.86-6.85(m, 1H), 2.03-1.98(m, 1H), 0.99-0.95(m, 4H); LCMS (electrospray) m/z 417.0 (M + H)+. B N-(6-(5-(thiophen-2-yl)-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 14 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.07(s, 1H), 12.62(s, 1H), 8.25(s, 1H), 8.08(s, 1H), 8.03(s, 1H), 7.77-7.67(m, 3H), 7.59(d, J = 8.0 Hz, 1H), 2.00- 1.96(m, 1H), 0.96-0.92(m, 4H); LCMS (electrospray) m/z 335.1 (M + H)+. A N-(6-(1H-indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 15 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27(s, 1H), 12.69(s, 1H), 8.21(s, 1H), 8.00(s, 1H), 7.84(d, J = 8.4 Hz, 1H), 7.65(dd, J = 8.4 Hz, J = 1.6 Hz, 1H), 7.54(dd, J = 10.8 Hz, J = 9.2 Hz, 1H), 2.02-1.96(m 1H), 0.95-0.93(m, 4H); LCMS (electrospray) m/z 353.1 (M + H)+. B N-(6-(5-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 16 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38(s, 1H), 12.74(s, 1H), 8.09(d, J = 1.6 Hz, 1H), 7.83(d, J = 8.8 Hz, 1H), 7.72(s, 1H), 7.55(d, J = 8.8 Hz, 1H), 7.51(dd, J = 8.4 Hz, J = 1.6 Hz, 1H), 7.46(d, J = 8.8 Hz, 1H), 2.02-1.97(m, 1H), 0.97-0.93(m, 4H); LCMS (electrospray) m/z 369.0 (M + H)+. B N-(6-(5-chloro-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 17 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.58(s, 1H), 12.74(s, 1H), 8.03(d, J = 1.6 Hz, 1H), 7.84(d, J = 8.0 Hz, 1H), 7.75(s, 2H), 7.71(s, 1H), 7.44(dd, J = 8.8 Hz, 1.6 Hz, 1H), 20.4-2.00(m, 1H), 0.99-0.96(m, 4H); LCMS (electrospray) m/z 403.0 (M + H)+. B N-(6-(5-(trifluoromethyl)-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 18 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.19(s, 1H), 12.64(s, 1H), 7.84(s, 1H), 7.75(s, 1H), 7.65(d, J = 8.0 Hz, 1H), 7.55(d, J = 8.0 Hz, 1H), 7.48(d, J = 8.0 Hz, 1H), 7.29-7.20(m, 3H), 6.63(d, J = 4.0 Hz, 1H), 3.66-3.62(m, 1H), 2.01-1.92(m, 1H), 0.98-0.85(m, 4H); LCMS (electrospray) m/z 417.1 (M + H)+. B N-(6-(5-(thiophen-3-yl)-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 19 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.75(s, 1H), 12.71(s, 1H), 8.35(s, 2H), 7.86(d, J = 6.8 Hz, 1H), 7.79(s, 1H), 7.53(d, J = 6.8 Hz, 1H), 7.28(d, J = 6.0 Hz, 1H), 2.05-1.95(m, 1H), 1.10-0.90(m, 4H); LCMS (electrospray) m/z 369.0 (M + H)+. B N-(6-(7-chloro-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 20 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36(s, 1H), 12.73(s, 1H), 8.39(s, 1H), 8.27(s, 1H), 7.88- 7.81(m, 2H), 7.62(s, 1H), 7.31(s, 1H), 2.04- 1.99(m, 1H), 0.99-0.97(m, 4H); LCMS (electrospray) m/z 369.0 (M + H)+. B N-(6-(6-chloro-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 21 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, NH), 12.70(s, NH), 7.95 (s, 1H), 7.84-7.82 (m, 2H), 7.75 (d, J = 8.4 Hz, 1H), 7.60(d, J = 9.6 Hz, 1H), 7.44(d, J = 10.0 Hz, 1H), 2.02-1.98(m, 1H), 1.08 (s, 9 H), 0.98-0.96 (m, 4H); LCMS (electrospray) m/z 435.1 (M + H)+. B tert-butyl 4-(2- (cyclopropanecarboxamido)benzo[d]thiazol- 6-yl)-1H-indazole-5-carboxylate 22 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.28(s, 1H), 12.74(s, 1H), 8.43(s, 1H), 8.23(s, 1H), 7.88- 7.87(m, 2H), 7.72-7.71(m, 2H), 7.61-7.59(m, 2H), 7.19(dd, J = 5.2 Hz, J = 3.2 Hz, 1H), 2.07-2.00(m, 1H), 1.01-0.97(m, 4H); LCMS (electrospray) m/z 417.0 (M + H)+. B N-(6-(6-(thiophen-2-yl)-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 23 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31 (s, NH), 12.71 (s, NH), 8.45-8.42 (m, 1H), 8.02 (s, 1H), 7.90 (s, 1H), 7.72-7.70 (d, J = 8.0 Hz, 1H), 7.48- 7.50 (d, J = 8.4 Hz, 1H), 7.46 (m, 4H), 6.76 (m, 1H), 4.24 (d, J = 5.2 Hz, 1H), 2.03-2.01 (m, 1H), 0.99-0.97 (m, 4H); LCMS (electrospray) m/z 474.1 (M + H)+. B 4-(2- (cyclopropanecarboxamido)benzo[d]thiazol- 6-yl)-N-(thiophen-3-ylmethyl)-1H- indazole-5-carboxamide 24 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.03(s, 1H), 12.67(s, 1H), 8.11(d, J = 3.2 Hz, 1H), 7.82-7.80(m, 2H), 7.60(dd, J = 8.4 Hz, J = 1.6 Hz, 1H), 7.53(d, J = 9.2 Hz, 1H), 7.34(d, J = 8.4 Hz, 1H), 3.75(s, 3H), 2.05-1.98(m, 1H), 0.98-0.96(m, 4H); LCMS (electrospray) m/z 365.1 (M + H)+. B N-(6-(5-methoxy-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 25 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.13(s, 1H), 12.72(s, 1H), 8.07(d, J = 1.6 Hz, 1H), 7.84(d, J = 8.0 Hz, 1H), 7.71(s, 1H), 7.58-7.53(m, 3H), 5.15- 5.08(m, 1H), 4.45(d, J = 5.2 Hz, 2H), 2.04-1.99(m, 1H), 1.02-0.96(m, 4H); LCMS (electrospray) m/z 365.0 (M + H)+. B N-(6-(5-(hydroxymethyl)-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 26 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.03 (s, NH), 12.77 (s, NH), 7.97 (s, 1H), 7.86 (d, J = 8.4 Hz, 1H), 7.49-7.38 (m, 3H), 4.20 (br, NH2), 2.10 (m, 1H), 1.99 (s, 3H), 0.99-0.96 (m, 4H); LCMS (electrospray) m/z 364.1 (M + H)+. B N-(6-(3-amino-5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide. 3 HCl 27 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.85 (s, 1H), 12.61 (s, 1H), 9.02 (s, 1H), 8.11 (s, 1H), 7.77-7.75 (m, 2H), 7.65 (d, J = 9.2 Hz, 1H), 7.34 (d, J = 8.6 Hz, 1H), 7.07 (d, J = 8.6 Hz, 1H), 1.97 (quin, J = 6.2 Hz, 1H), 0.94 (d, J = 6.0 Hz, 4H); LCMS (electrospray) m/z 351.40 (M + H)+. B N-(6-(5-hydroxy-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 28 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04(s, 1H), 12.69(s, 1H), 7.99(d, J = 1.2 Hz, 1H), 7.84(d, J = 8.4 Hz, 1H), 7.55(s, 1H), 7.50(d, J = 8.4 Hz, 1H), 7.42(dd, J = 7.6 Hz, 1.6 Hz, 1H), 7.35(d, J = 9.2 Hz, 1H), 2.0(q, J = 7.6 Hz, 2H), 2.05-1.99(m, 1H), 1.08(t, J = 7.6 Hz, 3H), 0.98-0.96(m, 4H); LCMS (electrospray) m/z 363.1 (M + H)+. B N-(6-(5-ethyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 29 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68(s, 1H), 12.76(s, 1H), 8.28(d, J = 1.6 Hz, 1H), 8.07(s, 1H), 7.89(d, J = 8.4 Hz, 1H), 7.75(d, J = 9.2 Hz, 1H), 7.69(dd, J = 8.4 Hz, J = 1.6 Hz, 2H), 2.03-1.96(m, 1H), 0.96-0.94(m, 4H); LCMS: m/z = 403.0 (M + H+)LCMS (electrospray) m/z 360.1 (M + H)+. B N-(6-(5-cyano-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide 30 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) 13.37(s, 1H), 12.76(s, 1H), 8.15(d, J = 1.6 Hz, 1H), 7.88(d, J = 8.4 Hz, 1H), 7.77(brs, 1H), 7.60-7.55(m, 2H), 7.50(d, J = 9.2 Hz, 1H), 5.16-4.95(m, 1H), 2.28-2.21(m, 1H), 1.81-1.71(m, 1H), 1.38-1.28(m, 1H); LCMS (electrospray) m/z 387.0 (M + H)+. B (1S,2S)-N-(6-(5-chloro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 31 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) 12.85(s, 1H), 12.76(s, 1H), 8.19 (s, 1H), 7.81-7.78 (m, 2H), 7.68 (d, J = 9.2 Hz, 1H), 7.56 (d, J = 8.6 Hz, 1H), 7.34 (d, J = 8.6 Hz, 1H), 5.16-4.95 (m, 1H), 4.26 (t, J = 4.4 Hz, 2H), 3.32 (t, J = 4.4 Hz, 2H), 2.45 (s, 6H), 2.28- 2.21(m, 1H), 1.78-1.68 (m, 1H), 1.38-1.28(m, 1H); LCMS (electrospray) m/z 440.10 (M + H)+. B (1S,2S)-N-(6-(5-(2- (dimethylamino)ethoxy)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 HCl 32 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.14 (s, NH), 13.08 (s, NH), 8.12 (s, 1H), 7.94-7.92 (m, 1H), 7.65 (s, 1H), 7.55 (dd, J12 = 1.6 Hz, J13 = 8.4 Hz, 1H), 7.47 (d, J = 8.4 Hz, 1H), 7.32 (d, J = 8.8 Hz, 1H), 2.75 (m, 1H), 2.31 (s, 3H), 1.21-1.17 (m, 4H); LCMS (electrospray) m/z 365.0 (M + H)+. A N-(6-(5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarbothioamide 33 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50(s, 1H), 12.85(s, 1H), 8.11(s, 1H), 7.91(d, J = 8.4 Hz, 2H), 7.85(s, 1H), 7.72(d, J = 4.0 Hz, 2H), 7.50(d, J = 8.8 Hz, 1H), 6.82(t, J = 55.2 Hz, 1H), 5.14-4.98(m, 1H), 2.25-2.22(m, 1H), 1.82-1.72(m, 1H), 1.37-1.30(m, 1H); 19F NMR (400 MHz, DMSO-d6) δ −102.50(d, J = 56.8 Hz, 1H), −103.08(d, J = 56.8 Hz, 1H), 219.66-219.92(m, 1H); LCMS (electrospray) m/z = 403.0 (M + H+) B (1S,2S)-N-(6-(5-(difluoromethyl)-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 34 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) 12.85(s, 1H), 12.77(s, 1H), 8.21 (s, 1H), 7.86 (s, 1H), 7.83 (d, J = 8.4 Hz, 1H), 7.68 (d, J = 8.4 Hz, 1H), 7.52 (d, J = 9.2 Hz, 1H), 7.32 (d, J = 9.2 Hz, 1H), 5.13-4.96 (m, 1H), 4.08 (t, J = 4.6 Hz, 2H), 3.53 (t, J = 4.4 Hz, 2H), 3.21 (s, 3H), 2.29-2.22(m, 1H), 1.80-1.70 (m, 1H), 1.36-1.27(m, 1H); LCMS (electrospray) m/z 427.10 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(5-(2- methoxyethoxy)-1H-indazol-4-yl) benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 2 HCl 35 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.22(s, 1H), 12.78(s, 1H), 8.02(d, J = 1.6 Hz, 1H), 7.86(d, J = 8.0 Hz, 1H), 7.77(d, J = 8.8 Hz, 1H), 7.70(s, 1H), 7.55(d, J = 8.8 Hz, 1H), 7.43(dd, J = 8.4 Hz, J = 2.0 Hz, 1H), 6.69(dd, J = 17.6 Hz, J = 10.8 Hz, 1H), 5.76(d, J = 16.4 Hz, 1H), 5.16(d, J = 12.0 hz, 1H), 5.13-4.94(m, 1H), 2.24-2.20(m, 1H), 1.72-1.71(m, 1H), 1.35-1.28(m, 1H); LCMS (electrospray) m/z = 379.1 (M + H+) B (1S,2S)-2-fluoro-N-(6-(5-vinyl-1H- indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 36 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.77(s, 1H), 8.13(dd, J = 4.4 Hz, 1.6 Hz, 1H), 7.92(dd, J = 8.4 Hz, 6.4 Hz, 1H), 7.88(d, J = 7.6 Hz, 1H), 7.64-7.54(m, 3H), 5.10-4.92(m, 1H), 5.39-5.27(m, 1H), 4.73- 4.60(m, 1H), 2.22-2.21(m, 1H), 1.69-1.68(m, 1H), 1.30-1.25(m, 1H); LCMS (electrospray) m/z = 383.1. (M + H+) B (1S,2S)-2-fluoro-N-(6-(5-(fluoromethyl)- 1H-indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide. 2 HCl 37 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.01(s, 1H), 12.74(s, 1H), 8.07(s, 1H), 7.83(dd, J = 8.4 Hz, 1H), 7.58(s, 1H), 7.51(d, J = 8.0 Hz, 1H), 7.41(d, J = 8.8 Hz, 1H), 6.95(dd, J = 8.4 Hz, 1.2 Hz, 1H), 5.10- 4.92(m, 1H), 2.21-2.17(m, 1H), 1.94-1.90(m, 1H), 1.74-1.69(m, 1H), 1.30-1.11(m, 1H), 0.82-0.75(m, 1H), 0.60-0.59(m, 1H); LCMS (electrospray) m/z = 393.1 (M + H+) B (1S,2S)-N-(6-(5-cyclopropyl-1H-indazol- 4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 38 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.79(s, 1H), 8.06(d, J = 2.0 Hz, 1H), 7.84(d, J = 8.0 Hz, 1H), 7.67(s, 1H), 7.55-7.53(m, 2H), 7.48(d, J = 8.8 Hz, 1H), 7.39(d, J = 1.2 Hz, 1H), 7.16(d, J = 8.8 Hz, 1H), 6.18-6.17(m, 1H), 5.29(s, 2H), 5.10-4.93(m, 1H), 2.23-2.20(m, 1H), 1.76-1.68(m, 1H), 1.31-1.27(m, 1H); LCMS (electrospray) m/z = 433.1 (M + H+) B (1S,2S)-N-(6-(5-((1H-pyrazol-1- yl)methyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 39 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35(s, 1H), 12.77(s, 1H), 8.20(d, J = 2.0 Hz, 1H), 7.87(s, 1H), 7.83(d, J = 8.4 Hz, 1H), 7.66(dd, J = 8.4 Hz, 1.6 Hz, 1H), 7.51(d, J = 3.2 Hz, 1H), 5.12-4.91(m, 1H), 3.91(s, 1H), 2.21-2.18(m, 1H), 1.75-1.68(m, 1H), 1.29-1.23(m, 1H); LCMS (electrospray) m/z = 377.1 (M + H+) B (1S,2S)-N-(6-(5-ethynyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 40 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, NH), 12.80 (s, NH), 8.09 (s, 1H), 7.88 (d, J = 8.0 Hz, 1H), 7.67 (s, 1H), 7.50 (d, J = 8.0 Hz, 1H), 7.35 (d, J = 9.6 Hz, 1H), 4.96-5.15 (m, 1H), 2.25-2.22 (m, 1H), 2.18 (s, 3H), 1.79-1.72 (m, 1H), 1.33-1.31 (m, 1H); LCMS (electrospray) m/z 385.1 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 41 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, NH), 12.80 (s, NH), 8.09 (s, 1H), 7.88 (d, J = 8.0 Hz, 1H), 7.67 (s, 1H), 7.50 (d, J = 8.0 Hz, 1H), 7.35 (d, J = 9.6 Hz, 1H), 4.96-5.15 (m, 1H), 2.25-2.22 (m, 1H), 2.18 (s, 3H), 1.79-1.72 (m, 1H), 1.33-1.31 (m, 1H); LCMS (electrospray) m/z 385.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 42 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.46 (s, NH), 12.83 (s, NH), 8.19 (s, 1H), 7.90 (d, J = 8.4 Hz, 1H), 7.80 (s, 1H), 7.64 (d, J = 8.8 Hz, 1H), 5.16- 4.95 (m, 1H), 2.28-2.21 (m, 1H), 1.79-1.72 (m, 1H), 1.35-1.28 (m, 1H); LCMS (electrospray) m/z = 405.0 (M + H+) B (1S,2S)-N-(6-(5-bromo-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 43 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.59 (s, NH), 12.79 (s, NH), 8.05 (s, 1H), 7.87 (d, J = 8.0 Hz, 1H), 7.71 s, 1H), 7.46-7.40 (m, 2H), 6.48 (dd, J12 = 11.8 Hz, J13 = 17.8 Hz, 1H), 5.35 (dd, J12 = 2.6 Hz, J13 = 14.2 Hz, 1H), 5.16-4.95 (m, 1H), 2.26-2.21 (m, 1H), 1.79-1.72 (m, 1H), 1.35-1.29 (m, 1H); LCMS (electrospray) m/z 449.0 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-vinyl- 1H-indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 44 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.34 (s, 1H), 12.77 (d, J = 3.2 Hz, 1H), 7.88 (d, J = 1.6 Hz, 1H), 7.80 (d, J = 8.4 Hz, 1H), 7.38 (d, J = 9.6 Hz, 1H), 7.30 (dd, J = 2.0, 6.4 Hz, 1H), 5.10 (m, 0.5H), 4.93 (m, 0.5H), 2.20 (m, 1H), 2.00 (m, 3H), 1.71 (m, 1H), 1.28 (m, 1H), LCMS (electrospray) m/z 419.05 (M + H)+. B (1S,2S)-N-(6-(3-chloro-6-fluoro-5-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 45 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (s, 1H), 12.79 (d, J = 3.6 Hz, 1H), 7.87 (d, J = 2.0 Hz, 1H), 7.86 (d, J = 7.6 Hz, 1H), 7.41 (d, J = 10.0 Hz, 1H), 7.28 (dd, J = 1.6 Hz, 1H), 5.14 (m, 0.5H), 4.97 (m, 0.5H), 2.23 (m, 1H), 2.00 (m, 3H), 1.76 (m, 1H), 1.31 (m, 1H), LCMS (electrospray) m/z 511.00 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-3-iodo-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide 46 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, NH), 12.80 (s, NH), 8.04 (s, 1H), 7.87 (d, J = 8.0 Hz, 1H), 7.56 (s, 1H), 7.44 (d, J = 8.4 Hz, 1H), 5.15-4.96 (m, 1H), 2.58-2.54 (m, 2H), 2.25-2.22 (m, 1H), 1.78- 1.72 (m, 1H), 1.33-1.30 (m, 1H), 1.06 (t, 3H); LCMS (electrospray) m/z 399.1 (M + H)+. B (1S,2S)-N-(6-(5-ethyl-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 47 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41(s, 1H), 12.78(s, 1H), 8.23(d, J = 1.6 Hz, 1H), 7.89(s, 1H), 7.84(d, J = 8.4 Hz, 1H), 7.67(d, J = 8.4 Hz, 1H), 7.46(d, J = 9.6 Hz, 1H), 5.11-4.92(m, 1H), 4.19(s, 1H), 2.21-2.18(m, 1H), 1.77-1.67(m, 1H), 1.33- 1.25(m, 1H); LCMS (electrospray) m/z 395.1 (M + H+) B (1S,2S)-N-(6-(5-ethynyl-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 48 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.34(s, 1H), 12.77(s, 1H), 8.01(d, J = 2.0 Hz, 1H), 7.84(d, J = 8.4 Hz, 1H), 7.60(s, 1H), 7.45(d, J = 8.4 Hz, 1H), 7.41(dd, J = 8.4 Hz, J = 1.2 Hz, 1H), 5.12-4.92(m, 1H), 2.21-2.19(m, 1H), 1.76-1.69(m, 1H), 1.31- 1.26(m, 1H); LCMS (electrospray) m/z 497.0 (M + H+) B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-iodo- 1H-indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 49 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (s, 1H), 12.78 (d, J = 3.6 Hz, 1H), 7.89 (d, J = 1.6 Hz, 1H), 7.84 (d, J = 8.4 Hz, 1H), 7.43 (d, J = 10 Hz, 1H), 7.31 (dd, J = 1.6, 6.8 Hz, 1H), 5.14 (m, 0.5H), 4.95 (m, 0.5H), 2.24 (m, 1H), 2.02 (t, J = 2.4 Hz, 3H), 1.75 (m, 1H), 1.31 (m, 1H); LCMS (electrospray) m/z 464.00 (M + H)+. B (1S,2S)-N-(6-(3-bromo-6-fluoro-5-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 50 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67(s, 1H), 12.82(s, 1H), 8.03(s, 1H), 7.82(d, J = 8.4 Hz, 1H), 7.66-7.64(m, 1H), 7.41(d, J = 8.4 Hz, 1H), 5.15- 4.95(m, 1H), 2.26-2.23(m, 1H), 1.79-1.72(m, 1H), 1.34-1.28(m, 1H); LCMS (electrospray) LCMS: m/z 439.1 (M + H+) B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5- (trifluoromethyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide 51 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.75 (s, 1H), 12.82 (s, 1H), 8.09 (d, J = 1.6 Hz, 1H), 7.88 (d, J = 8.4 Hz, 1H), 7.79 (brs, 1H), 7.50 (dd, J = 1.6, 6.4 Hz, 1H), 5.14 (m, 0.5H), 4.97 (m, 0.5H), 2.23 (m, 4H), 1.76 (m, 1H), 1.32 (m, 1H); LCMS (electrospray) m/z 419.00 (M + H)+. B (1S,2S)-N-(6-(7-chloro-6-fluoro-5-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 52 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 12.81 (s, 1H), 7.91 (d, J = 1.6 Hz, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.33 (m, 2H), 5.73 (m, 1H), 5.59 (m, 1H), 5.14 (m, 0.5H), 4.97 (m, 0.5H), 4.84 (m, 1H), 2.25 (m, 1H), 2.01 (t, J = 2.4 Hz, 3H) 1.76 (m, 1H), 1.32 (m, 1H); LCMS (electrospray) m/z 411.10 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 3-vinyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide 53 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.00(s, 1H), 12.80(s, 1H), 7.92(d, J = 1.2 Hz, 1H), 7.84(d, J = 8.4 Hz, 1H), 7.34(dd, J = 8.4 Hz, J = 1.6 Hz, 1H), 5.15- 4.97(m, 1H), 2.26-2.24(m, 1H), 2.08(s, 3H), 1.79- 1.76(m, 1H), 1.32-1.27(m, 1H); LCMS (electrospray) m/z 454.0 (M + H+) B (1S,2S)-N-(6-(3,7-dichloro-6-fluoro-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)-2-fluorocyclopropane-1-carboxamide 54 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.03(s, 1H), 13.21(s, 1H), 7.94(d, J = 1.6 Hz, 1H), 7.50(d, J = 1.6 Hz, 1H), 5.14-4.95(m, 1H), 2.25-2.22(m, 1H), 2.09(s, 3H), 1.80-1.70(m, 1H), 1.36-1.29(m, 1H); LCMS (electrospray) m/z 487.0 (M + H+) B (1S,2S)-N-(4-chloro-6-(3,7-dichloro-6- fluoro-5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 55 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.33(s, 1H), 12.80(s, 1H), 8.06(s, 1H), 7.84(d, J = 8.0 Hz, 1H), 7.43-7.41(m, 1H), 5.13-4.97(m, 1H), 2.23-2.20(m, 1H), 2.16(s, 3H), 1.77-1.72(m, 1H), 1.44-1.41(m, 1H); LCMS (electrospray): m/z 421.0 (M + H+) B (1S,2S)-2-fluoro-N-(6-(3,6,7-trifluoro-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide 56 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.78 (s, 1H), 12.60 (s, 1H), 8.09 (s, 1H), 8.06 (s, 1H), 7.84 (d, J = 8.0 Hz, 1H), 7.43-7.41 (m, 1H), 5.13-4.97 (m, 1H), 2.23-2.20 (m, 1H), 2.16 (s, 3H), 1.77-1.72 (m, 1H), 1.44-1.41 (m, 1H); LCMS (electrospray): m/z 403.0 (M + H)+. B (1S,2S)-N-(6-(6,7-difluoro-5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 57 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.59 (s, 1H), 12.81 (s, 1H), 8.15 (s, 1H), 7.88 (d, J = 8.0 Hz, 1H), 7.82 (s, 1H), 7.34 (dd, J = 8.4 Hz, J = 1.6 Hz, 1H), 5.18-5.12 (m, 0.5H), 5.01-4.96 (m, 0.5H), 2.50 (t, J = 1.6 Hz, 3H), 2.29-2.21 (m, 1H), 1.85-1.72 (m, 1H), 1.38-1.29 (m, 1H); LCMS (electrospray) m/z 419.0 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 58 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (br s, 1H), 12.82 (br s, 1H), 8.19 (d, J = 1.7 Hz, 1H), 7.96-7.82 (m, 2H), 7.59 (dd, J = 1.8, 8.4 Hz, 1H), 5.26-4.85 (m, 1H), 2.57 (s, 3H), 2.30-2.19 (m, 1H), 1.84- 1.69 (m, 1H), 1.33 (tdd, J = 6.4, 9.0, 12.9 Hz, 1H); LCMS (electrospray) m/z 450.8 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 59 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (s, 1H), 12.77 (br s, 1H), 8.04 (s, 1H), 7.87 (dd, J12 = 4.8 Hz, J13 = 8.4 Hz, 1H), 7.66 (s, 1H), 7.45 (d, J = 7,6 Hz, 1H), 5.14-4.95 (m, 1H), 2.49 (d, J = 1.7 Hz, 3H), 2.21 (d, J = 2.8 Hz, 3H), 2.18-2.10 (m, 1H), 1.75-1.61 (m, 1H), 1.27-1.10 (m, 1H); LCMS (electrospray) m/z 399.1 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7- dimethyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide. 2 TFA 60 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.87 (s, 1H), 12.85 (s, 1H), 8.22 (s, 1H), 7.88 (m, 2H), 7.60 (dd, J12 = 1.8 Hz, J13 = 8.2 Hz, 1H), 5.13-4.97 (m, 1H), 2.28-2.21 (m, 1H), 1.95 (s, 3H), 1.92 (s, 3H), 1.81- 1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS (electrospray) m/z 481.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7- (dimethylphosphoryl)-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 61 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70 (s, 1H), 12.82 (s, 1H), 8.19 (d, J = 2.0 Hz, 1H), 7.90 (d, J = 8.4 Hz, 2H), 7.59 (dd, J = 6.8 Hz, J = 2.0 Hz, 1H), 7.10 (q, J = 12.4 Hz, 1H), 6.22 (brs, 1H), 5.81 (d, J = 11.6 Hz, 1H), 5.16-5.12 (m, 0.5H), 4.99-4.96 (m, 0.5H), 2.28-2.21 (m, 1H), 1.81-1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS (electrospray) m/z 431.0 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-vinyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 62 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.37 (s, 1H), 12.79 (s, 1H), 8.08 (s, 1H), 7.88 (d, J = 8.4 Hz, 1H), 7.49 (d, J = 8.0 Hz, 1H), 7.11-7.09 (m, 1H), 6.16 (d, J = 18.4 Hz, 1H), 5.70 (d, J = 12.0 Hz, 1H), 5.14-4.97 (m, 1H), 2.28-2.21 (m, 1H), 2.20 (s, 3H), 1.81-1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS (electrospray) m/z 411.1 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-vinyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide 63 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.85 (s, 1H), 8.22 (s, 1H), 7.96-7.89 (m, 2H), 7.49 (d, J = 8.0 Hz, 1H), 7.11-7.09 (m, 1H), 7.60 (d, J = 8.0 Hz, 1H), 5.14-4.97 (m, 1H), 3.19 (s, 3H), 2.28-2.21 (m, 1H), 1.79-1.73 (m, 1H), 1.37-1.28 (m, 1H); LCMS (electrospray) m/z 467.0 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylsulfinyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl salt 64 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.79 (br s, 1H), 8.08 (s, 1H), 7.87 (d, J = 8.0 Hz, 1H), 7.73 (s, 1H), 7.49 (d, J = 9.6 Hz, 1H), 5.14-4.96 (m, 1H), 3.17 (s, 3H), 2.54 (s, 3H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 431.0 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide 65 01embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.44- 8.32 (m, 2H), 7.84-7.76 (m, 1H), 7.42-7.25 (m, 5H), 5.07-5.01 (m, 1H), 3.27-2.97 (m, 5H), 2.24- 2.15 (m, 1H), 2.06 (br d, J = 2.2 Hz, 3H), 1.96- 1.81 (m, 1H), 1.38-1.28 (m, 1H); LCMS (electrospray) m/z 490.2 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 1H-indazol-4-yl)-7-(2-(pyridin-4- yl)ethyl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide. 3 TFA 66 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (br s, 1H), 12.81 (s, 1H), 8.12 (s, 1H), 7.90 (d, J = 8.4 Hz, 1H), 7.51 (d, J = 8.4 Hz, 1H), 5.14-4.96 (m, 1H), 3.13 (s, 3H), 2.32 (s, 3H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 447.1 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylsulfinyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 2 HCl 67 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 12.79 (s, 1H), 8.08 (s, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.83 (br s, 1H), 7.48 (dd, J = 1.6, 6.8 Hz, 1H), 5.14- 4.96 (m, 1H), 2.26-2.18 (m, 4H), 1.82-1.71 (m, 1H), 1.36-1.28 (m, 1H); LCMS (electrospray) m/z 511.00 (M + H)+. B (1S,2S)-2-fluoro-N-(6-(6-fluoro-7-iodo-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropane-1-carboxamide 68 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.94 (s, 1H), 12.76 (s, 1H), 8.08 (d, J = 1.6 Hz, 1H), 7.84 (d, J = 8.4 Hz, 1H), 7.71 (s, 1H), 7.52 (dd, J = 2.4, 6.4 Hz, 1H), 5.69 (s, 2H), 5.16-4.94 (m, 1H), 2.27- 2.20 (m, 1H), 1.81-1.70 (m, 1H), 1.36-1.27 (m, 1H); LCMS (electrospray) m/z 420.00 (M + H)+. B (1S,2S)-N-(6-(7-amino-5-chloro-6-fluoro- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 69 05embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (s, 1H), 12.79 (s, 1H), 8.13 (d, J = 1.6 Hz, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.76 (s, 1H), 7.55 (dd, J = 1.6, 6.8 Hz, 1H), 5.16-4.95 (m, 1H), 2.99 (s, 6H), 2.28- 2.21 (m, 1H), 1.81-1.71 (m, 1H), 1.36-1.28 (m, 1H); LCMS (electrospray) m/z 448.10 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 70 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70 (br s, 1H), 12.81 (s, 1H), 8.15 (s, 1H), 7.96 (br s, 2H), 7.90- 7.86 (m, 2H), 7.55 (d, J = 8.4 Hz, 1H), 5.11-4.92 (m, 1H), 3.14 (m, 2H), 2.88 (m, 2H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25- 1.11 (m, 1H); LCMS (electrospray) m/z 480.1 (M + H)+. B (1S,2S)-N-(6-(7-((2-aminoethyl)thio)-5- chloro-6-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 HCl 71 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (s, 1H), 12.82 (s, 1H), 8.17 (d, J = 0.8 Hz, 1H), 7.88 (s, 1H), 7.86 (d, J = 8.4 Hz, 1H), 7.58 (dd, J = 1.6, 6.8 Hz, 1H), 5.14-4.94 (m, 1H), 3.50 (t, J = 6.0 Hz, 2H), 3.20 (s, 3H), 3.17 (t, J = 6.4 Hz, 2H), 2.26-2.19 (m, 1H), 1.80-1.70 (m, 1H), 1.35-1.26 (m, 1H); LCMS (electrospray) m/z 495.10 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2- methoxyethyl)thio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 72 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.29 (s, 1H), 10.42 (s, 1H), 7.80 (s, 1H), 7.75 (d, J = 1.6 Hz, 1H), 7.49 (d, J = 8.4 Hz, 1H), 7.31 (dd, J = 1.6, 6.8 Hz, 1H), 6.58 (q, J = 10 Hz, 1H), 6.32 (dd, J = 1.6, 15.2 HZ, 1H), 5.83 (d, J = 10 Hz, 1H), 4.86-4.65 (m, 1H), 1.95 (d, J = 14 Hz, 1H), 1.85 (m, 1H), 1.69- 1.55 (m, 1H), 0.95-0.87 (m, 1H); LCMS (electrospray) m/z 474.00 (M + H)+. B (1S,2S)-N-(6-(7-acrylamido-5-chloro-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide 73 09embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.78 (br s, 1H), 12.81 (s, 1H), 8.18 (s, 1H), 7.99 (t, J = 5.2 Hz, 1H), 7.89-7.87 (m, 2H), 7.59 (d, J = 8.4 Hz, 1H), 5.13- 4.96 (m, 1H), 3.29 (m, 2H), 3.00 (m, 2H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.75 (s, 3H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 522.1 (M + H)+. B (1S,2S)-N-(6-(7-((2-acetamidoethyl)thio)- 5-chloro-6-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 74 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (br s, 1H), 12.82 (s, 1H), 8.14 (s, 1H), 7.88 (d, J = 8.4 Hz, 1H), 7.81 (s, 1H), 7.55 (d, J = 8.4 Hz, 1H), 5.14-4.76 (m, 1H), 3.83 (m, 4H), 3.28 (m, 4H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 490.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- morpholino-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl 75 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.60 (s, 1H), 12.82 (s, 1H), 8.13 (s, 1H), 7.88 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.54 (d, J = 8.4 Hz, 1H), 5.16-4.97 (m, 1H), 3.55 (br s, 6H), 3.39 (br s, 2H), 2.90 (d, J = 8.0 Hz, 3H), 2.19-2.10 (m, 1H), 1.73-1.60 (m, 1H), 1.35-1.28 (m, 1H); LCMS (electrospray) m/z 503.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(4- methylpiperazin-1-yl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 HCl 76 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56 (s, 1H), 12.82 (s, 1H), 8.71 (br s, 1H), 8.13 (s, 1H), 7.89 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.54 (d, J = 8.4 Hz, 1H), 5.13-4.98 (m, 1H), 3.38 (br s, 4H), 2.66 (br s, 4H), 2.19-2.10 (m, 1H), 1.79-1.73 (m, 1H), 1.35-1.28 (m, 1H); LCMS (electrospray) m/z 489.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (piperazin-1-yl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 TFA 77 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (s, 1H), 12.78 (s, 1H), 8.08 (s, 1H), 7.84 (d, J = 8.4 Hz, 1H), 7.73 (s, 1H), 7.51 (d, J = 8.4 Hz, 1H), 5.12-4.96 (m, 1H), 3.65 (br s, 4H), 2.19-2.10 (m, 1H), 1.95 (br s, 4H), 1.77-1.73 (m, 1H), 1.35-1.28 (m, 1H); LCMS (electrospray) m/z 473.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (pyrrolidin-1-yl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 78 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.17 (s, 1H), 12.79 (s, 1H), 8.09 (s, 1H), 7.85 (d, J = 8.4 Hz, 1H), 7.75 (s, 1H), 7.83 (d, J = 6.4, Hz, 1H), 5.14-4.97 (m, 2H), 4.41 (s, 1H), 3.97 (s, 2H), 3.73-3.35 (m, 2H), 2.29-2.18 (m, 1H), 2.10-1.98 (m, 1H), 1.94- 1.85 (m, 1H), 1.82-1.70 (m, 1H), 1.38-1.27 (m, 1H); LCMS (electrospray) m/z 490.10 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(3- hydroxypyrrolidin-1-yl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 79 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.75 (s, 1H), 12.84 (s, 1H), 8.20 (s, 1H), 7.94-7.82 (m, 2H), 7.60 (d, J = 8.4 Hz, 1H), 7.83 (d, J = 6.4, Hz, 1H), 5.18-4.87 (m, 2H), 3.52 (q, J = 5.2 Hz, 2H), 3.06 (t, J = 5.6 Hz, 2H), 2.29-2.18 (m, 1H), 1.83-1.69 (m, 1H), 1.39-1.27 (m, 1H); LCMS (electrospray) m/z 481.05 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2- hydroxyethyl)thio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 80 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.78 (br s, 1H), 12.81 (s, 1H), 8.14 (d, J = 1.4 Hz, 1H), 7.88 (d, J = 8.4 Hz, 1H), 7.86-7.79 (m, 1H), 7.55 (dd, J = 1.8, 8.4 Hz, 1H), 5.25-4.85 (m, 1H), 4.15 (s, 3H), 2.30- 2.18 (m, 1H), 1.85-1.68 (m, 1H), 1.33 (tdd, J = 6.4, 9.0, 12.7 Hz, 1H); LCMS (electrospray) m/z 435.3 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- methoxy-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 81 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.77 (s, 1H), 12.82 (s, 1H), 8.16 (d, J = 1.5 Hz, 1H), 7.92-7.87 (m, 1H), 7.84-7.80 (m, 1H), 7.62-7.53 (m, 1H), 5.27-4.92 (m, 1H), 4.38 (q, J = 7.0 Hz, 2H), 2.30- 2.20 (m, 1H), 1.88-1.71 (m, 1H), 1.42 (t, J = 7.0 Hz, 3H), 1.38-1.29 (m, 1H); LCMS (electrospray) m/z 449.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7-ethoxy-6-fluoro- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 82 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.91 (s, 1H), 7.74 (s, 1H), 7.66 (d, J = 8.4 Hz, 1H), 7.40 (dd, J = 1.6, 6.8, Hz, 1H), 5.02-4.78 (m, 1H), 3.23 (t, J = 5.6 Hz, 2H), 2.99 (d, J = 4 Hz, 3H), 2.80 (t, J = 6.0 2H), 2.09-1.99 (m, 1H), 1.74-1.62 (m, 1H), 1.16-1.07 (m, 1H); LCMS (electrospray) m/z 477.10 (M + H)+. B (1S,2S)-N-(6-(7-((2- aminoethyl)(methyl)amino)-5-chloro-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide 83 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.07 (d, J = 1.6 Hz, 1H), 7.82 (d, J = 8.0 Hz, 1H), 7.78 (s, 1H), 7.51 (dd, J = 2.0, 6.4 Hz, 1H), 5.14-4.91 (m, 1H), 3.48 (m, 2H), 3.16 (t, J = 12 Hz 2H), 2.87-2.78(m, 1H), 2.24-2.15 (m, 1H), 1.85 (d, J = 10.4 Hz, 2H), 1.80- 1.68 (m, 1H), 1.66-1.54 (m, 2H), 1.33-1.24 (m, 1H); LCMS (electrospray) m/z 503.10 (M + H)+. B (1S,2S)-N-(6-(7-(4-aminopiperidin-1-yl)- 5-chloro-6-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 84 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.10 (d, J = 1.6 Hz, 1H), 7.85 (d, J = 8.4 Hz, 1H), 7.79 (s, 1H), 7.53 (dd, J = 1.6, 8.0 Hz, 1H), 5.15-4.93 (m, 1H), 3.26- 3.17 (m, 2H), 3.12-2.96 (m, 2H), 2.89-2.81 (m, 1H), 2.26-2.17 (m, 1H), 1.91-1.68 (m, 4H), 1.35- 1.23 (m, 2H); LCMS (electrospray) m/z 503.1 (M + H)+. B (1S,2S)-N-(6-(7-(3-aminopiperidin-1-yl)- 5-chloro-6-fluoro-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 85 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94 (s, 1H), 12.83 (s, 1H), 8.15 (s, 1H), 7.89 (d, J = 8.0 Hz, 1H), 7.82 (s, 1H), 7.56 (d, J = 8.0 Hz, 1H), 5.14-4.97 (m, 1H), 3.61 (s, 3H), 3.41-3.38 (m, 2H), 2.87- 2.84 (m, 2H), 2.78 (s, 6H), 2.26-2.23 (m, 1H), 1.73- 1.65 (m, 1H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 505.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7-((2- (dimethylamino)ethyl)(methyl)amino)-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide. 3 HCl 86 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94 (s, 1H), 12.85 (s, 1H), 8.19 (s, 1H), 7.89 (d, J = 8.0 Hz, 1H), 7.82 (s, 1H), 7.60 (d, J = 8.0 Hz, 1H), 5.14-4.97 (m, 1H), 3.61-3.57 (m, 2H), 3.04-3.01 (m, 2H), 2.87-2.84 (m, 2H), 2.26-2.23 (m, 1H), 1.73-1.65 (m, 1H), 1.64-1.61 (m, 2H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 495.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((3- hydroxypropyl)thio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropanecarboxamide. 2 HCl 87 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.86 (s, 1H), 12.84 (s, 1H), 8.19 (d, J = 1.6 Hz, 1H), 8.13-8.05 (m, 1H), 7.95-7.85 (m, 2H), 7.59 (dd, J = 1.6, 8.4 Hz, 1H), 5.18-4.95 (m, 1H), 3.66 (s, 2H), 2.58 (d, J = 1.4 Hz, 3H), 2.29-2.21 (m, 1H), 1.83-1.69 (m, 1H), 1.38-1.28 (m, 1H); LCMS (electrospray) m/z 509.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2- (methylamino)-2-oxoethyl)thio)-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropanecarboxamide 88 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56 (s, 1H), 12.83 (s, 1H), 8.19 (d, J = 1.6 Hz, 1H), 7.93-7.81 (m, 2H), 7.59 (dd, J = 2.0, 8.0 Hz, 1H), 7.20 (s, 1H), 5.17-4.95 (m, 2H), 4.01 (s, J = 8.8 Hz, 1H), 3.91-3.82 (m, 1H), 3.67-3.60 (m, 1H), 3.55 (t, J = 5.2 Hz, 2H), 2.29-2.21 (m, 1H), 1.83-1.70 (m, 1H), 1.38-1.28 (m, 1H); LCMS (electrospray) m/z 519.1 (M + H)+. B (1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazol-7-yl)azetidin-3-yl)carbamic acid 89 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.25 (s, 1H), 12.78 (s, 1H), 8.09 (d, J = 1.6 Hz, 1H), 7.90-7.70 (m, 2H), 7.52 (dd, J = 1.6, 8.4 Hz, 1H), 7.20 (s, 1H), 5.67-5.47 (s, 1H), 5.17-4.93 (m, 1H), 4.43- 4.16 (m, 2H), 4.04-3.96 (m, 1H), 3.89-3.52 (m, 2H), 2.86 (s, 3H), 2.29-2.20 (m, 1H), 1.83-1.68 (m, 1H), 1.38-1.27 (m, 1H); LCMS (electrospray) m/z 533.1 (M + H)+ B (1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazol-7-yl)azetidin-3- yl)(methyl)carbamic acid 90 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.13 (s, 1H), 12.78 (s, 1H), 8.10 (d, J = 1.6 Hz, 1H), 7.89-7.68 (m, 2H), 7.52 (dd, J = 2.4, 8.8 Hz, 1H), 7.21 (s, 1H), 5.82-5.62 (s, 1H), 5.17-4.94 (m, 1H), 4.33- 4.23 (m, 1H), 4.15-4.06 (m, 1H), 3.67-3.43 (m, 2H), 3.34-3.26 (m, 1H), 3.12-3.05 (m, 1H), 2.31- 2.15 (m, 2H), 1.84-1.69 (m, 1H), 1.39-1.26 (m, 1H); LCMS (electrospray) m/z 533.1 (M + H)+. B ((1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazol-7-yl)azetidin-3- yl)methyl)carbamic acid 91 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.85 (s, 1H), 7.76 (s, 1H), 7.63 (d, J = 8.4 Hz, 1H), 7.36 (dd, J = 1.6, 8.4 Hz, 1H), 5.02-4.78 (m, 1H), 4.04-3.87 (m, 1H), 3.78-3.61 (m, 2H), 3.58-3.48 (m, 1H), 2.72-2.59 (m, 2H), 2.34-2.26 (m, 1H), 2.09-1.92 (m, 2H), 1.74-1.61 (m, 4H), 1.15-1.02 (m, 1H); LCMS (electrospray) m/z 503.1 (M + H)+. B (1S,2S)-N-(6-(7-(3- (aminomethyl)pyrrolidin-1-yl)-5-chloro-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropanecarboxamide 92 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 12.82 (s, 1H), 8.22 (s, 1H), 8.14 (s, 1H), 7.90 (d, J = 8.0 Hz, 1H), 7.85 (s, 1H), 7.55 (d, J = 8.0 Hz, 1H), 5.14-4.97 (m, 1H), 2.89 (m, 2H), 2.65 (t, J = 5.2 Hz, 2H), 2.26-2.23 (m, 1H), 1.73-1.65 (m, 1H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 491.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(2-(methylamino)ethyl)amino)-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 93 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 12.81 (s, 1H), 8.22 (s, 1H), 8.14 (s, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.78 (s, 1H), 7.55 (d, J = 8.8 Hz, 1H), 5.14-4.96 (m, 1H), 3.64-3.61 (m, 2H), 3.35- 3.32 (m, 2H), 3.02 (s, 3H), 2.26-2.23 (m, 1H), 1.73- 1.65 (m, 1H), 1.31-1.23 (m, 1H); LCMS (electrospray) m/z 478.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2- hydroxyethyl)(methyl)amino)-1H-indazol- 4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropanecarboxamide. 2 HCl 94 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 12.82 (s, 1H), 8.49 (br, 1H), 8.38 (br, 1H), 8.14 (s, 1H), 7.89 (d, J = 8.4 Hz, 1H), 7.72 (s, 1H), 7.55 (d, J = 8.8 Hz, 1H), 5.16-4.97 (m, 1H), 3.96-3.91 (m, 2H), 3.67-3.64 (m, 2H), 2.90 (s, 3H), 2.26-2.23 (m, 1H), 1.79-1.72 (m, 1H), 1.37-1.30 (m, 1H), 1.08 (t, J = 7.2 Hz, 1H); LCMS (electrospray) m/z 503.1 (M + H)+. B (1S,2S)-N-(6-(7-((azetidin-3- ylmethyl)(methyl)amino)-5-chloro-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropanecarboxamide. 3 TFA 95 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (s, 1H), 12.78 (s, 1H), 8.57 (br, 2H), 8.08 (s, 1H), 7.85 (d, J = 8.4 Hz, 1H), 7.77 (s, 1H), 7.51 (dd, J = 8.0 Hz, J = 1.6 Hz, 1H), 5.16-4.95 (m, 1H), 4.00 (m, 2H), 3.92 (m, 2H), 3.71 (br, 2H), 3.05 (br, 1H), 2.25- 2.20 (m, 1H), 1.78-1.68 (m, 1H), 1.36-1.28 (m, 1H), 1.08 (t, J = 7.2 Hz, 1H); LCMS (electrospray) m/z 489.1 (M + H)+. B (1S,2S)-N-(6-(7-((azetidin-3- ylmethyl)amino)-5-chloro-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropanecarboxamide. 3 TFA 96 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26 (br s, 1H), 12.74 (s, 1H), 8.00 (d, J = 1.4 Hz, 1H), 7.83 (d, J = 8.3 Hz, 1H), 7.60 (s, 1H), 7.44 (dd, J = 1.7, 8.3 Hz, 1H), 6.81 (s, 1H), 5.16-4.94 (m, 1H), 3.98 (s, 3H), 2.31 (s, 3H), 2.27-2.19 (m, 1H), 1.82-1.68 (m, 1H), 1.32 (tdd, J = 6.3, 9.0, 12.8 Hz, 1H); LCMS(electrospray) m/z 397.4 (M + H+). B (1S,2S)-2-fluoro-N-(6-(7-methoxy-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)cyclopropanecarboxamide. 2 TFA 97 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 12.76 (s, 1H), 8.04 (d, J = 1.3 Hz, 1H), 7.86 (d, J = 8.3 Hz, 1H), 7.69 (s, 1H), 7.46 (dd, J = 1.7, 8.3 Hz, 1H), 5.18-4.89 (m, 1H), 4.08 (d, J = 0.9 Hz, 3H), 2.29-2.22 (m, 1H), 2.20 (d, J = 3.2 Hz, 3H), 1.83-1.69 (m, 1H), 1.32 (tdd, J = 6.4, 8.8, 12.8 Hz, 1H); LCMS(electrospray) m/z 415.4 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- methoxy-5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2- yl)cyclopropanecarboxamide. 2 TFA 98 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) 13.42 (br s, 1H), 12.78 (s, 1H), 8.05 (d, J = 1.3 Hz, 1H), 7.86 (d, J = 8.3 Hz, 1H), 7.68 (s, 1H), 7.47 (dd, J = 1.5, 8.3 Hz, 1H), 5.22-4.90 (m, 1H), 4.30 (br d, J = 7.1 Hz, 2H), 2.23 (br d, J = 7.0 Hz, 1H), 2.19 (d, J = 3.1 Hz, 3H), 1.80-1.70 (m, 1H), 1.39 (t, J = 7.0 Hz, 3H), 1.35-1.28 (m, 1H); LCMS(electrospray) m/z 429.4 (M + H+). B (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)-2-fluorocyclopropanecatboxamide. 2 TFA 99 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (s, 1H), 12.84 (s, 1H), 8.19 (d, J = 2.0 Hz, 1H), 7.94-7.84 (m, 2H), 7.59 (dd, J = 1.6, 8.0 Hz, 1H), 5.17-4.95 (m, 1H), 4.03 (s, 2H), 3.01 (s, 3H), 2.81 (s, 3H), 2.29-2.20 (m, 1H), 1.82-1.70 (m, 1H), 1.38-1.28 (m, 1H); LCMS (electrospray) m/z 522.10 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7-((2- (dimethylamino)-2-oxoethyl)thio)-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide 100 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 12.80 (s, 1H), 8.12 (s, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.77 (s, 1H), 7.54 (dd, J = 8.0 Hz, J = 1.6 Hz, 1H), 5.14-4.96 (m, 1H), 3.62 (s, 2H), 3.37 (s, 6H), 3.15 (s, 3H), 2.25-2.20 (m, 1H), 1.78-1.68 (m, 1H), 1.34-1.28 (m, 1H); LCMS (electrospray) m/z 519.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-7-((2- (dimethylamino)-2- oxoethyl)(methyl)amino)-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 101 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.22 (br s, 1H), 12.74 (s, 1H), 8.00 (d, J = 1.3 Hz, 1H), 7.83 (d, J = 8.3 Hz, 1H), 7.60 (s, 1H), 7.44 (dd, J = 1.8, 8.3 Hz, 1H), 6.79 (s, 1H), 5.17-4.93 (m, 1H), 4.27 (q, J = 7.1 Hz, 2H), 2.29 (s, 3H), 2.27-2.20 (m, 1H), 1.82- 1.69 (m, 1H), 1.46 (t, J = 7.0 Hz, 3H), 1.32 (tdd, J = 6.4, 8.9, 12.8 Hz, 1H); LCMS(electrospray) m/z 410.9 (M + H+). B (1S,2S)-N-(6-(7-ethoxy-5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 102 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (br s, 1H), 12.77 (s, 1H), 8.00 (d, J = 1.6 Hz, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.55 (s, 1H), 7.42 (dd, J = 1.6, 8.3 Hz, 1H), 5.18-4.93 (m, 1H), 2.96 (s, 3H), 2.96 (s, 3H), 2.56-2.52 (m, 2H), 2.29-2.20 (m, 1H), 1.82- 1.71 (m, 1H), 1.32 (tdd, J = 6.6, 9.0, 12.8 Hz, 1H), 1.07 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 442.2 (M + H+). B (1S,2S)-N-(6-(7-(dimethylamino)-5-ethyl- 6-fluoro-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 103 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 12.80 (s, 1H), 8.05 (d, J = 1.3 Hz, 1H), 7.88 (d, J = 8.1 Hz, 1H), 7.64 (s, 1H), 7.45 (dd, J = 1.8, 8.3 Hz, 1H), 5.18-4.92 (m, 1H), 2.59 (br d, J = 6.9 Hz, 2H), 2.52 (br s, 3H), 2.29-2.20 (m, 1H), 1.82- 1.70 (m, 1H), 1.37-1.28 (m, 1H), 1.08 (t, J = 7.3 Hz, 3H); LCMS(electrospray) m/z 445.3 (M + H+). B (1S,2S)-N-(6-(5-ethyl-6-fluoro-7- (methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 104 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (br s, 1H), 12.77 (br s, 1H), 8.03 (s, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.64 (s, 1H), 7.46 (br d, J = 8.3 Hz, 1H), 5.18- 4.89 (m, 1H), 2.95 (s, 6H), 2.28-2.22 (m, 1H), 2.16 (br d, J = 3.2 Hz, 3H), 1.83-1.69 (m, 1H), 1.38- 1.24 (m, 1H); LCMS(electrospray) m/z 428.2 (M + H+). B (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 105 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 12.79 (br s, 1H), 8.09 (d, J = 1.6 Hz, 1H), 7.86 (d, J = 8.3 Hz, 1H), 7.71 (s, 1H), 7.51 (dd, J = 1.8, 8.3 Hz, 1H), 7.48 (d, J = 9.3 Hz, 1H), 5.21-4.92 (m, 1H), 2.28-2.22 (m, 1H), 2.21 (s, 3H), 1.83-1.69 (m, 1H), 1.32 (ddd, J = 2.6, 6.4, 12.8 Hz, 1H); LCMS(electrospray) m/z 417.1 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5- (methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 2 TFA 106 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.84 (br s, 1H), 12.79 (s, 1H), 8.03 (d, J = 1.6 Hz, 1H), 7.88 (d, J = 8.3 Hz, 1H), 7.70 (br s, 1H), 7.43 (dd, J = 1.8, 8.3 Hz, 1H), 5.23-4.89 (m, 1H), 2.61 (br d, J = 6.0 Hz, 2H), 2.29-2.20 (m, 1H), 1.82-1.69 (m, 1H), 1.37- 1.27 (m, 1H), 1.09 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 417.1 (M + H+). B (1S,2S)-N-(6-(5-ethyl-6,7-difluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 107 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43 (s, 1H), 12.78 (s, 1H), 8.02 (s, 1H), 7.87 (d, J = 8.4 Hz, 1H), 7.59 (s, 1H), 7.45-7.42 (m, 1H), 5.15-4.97 (m, 1H), 4.34-4.28 (m, 2H), 2.59-2.53 (m, 2H), 2.27- 2.23 (m, 1H), 1.85-1.75 (m, 1H), 1.40 (t, J = 6.8 Hz, 3H), 1.36-1.32 (m, 1H), 1.09 (t, J = 7.2 Hz, 3H); LCMS(electrospray) m/z 443.2 (M + H+). B (1S,2S)-N-(6-(7-ethoxy-5-ethyl-6-fluoro- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 108 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27 (s, 1H), 12.82 (s, 1H), 10.11 (s, 1H), 8.20 (d, J = 1.6 Hz, 1H), 7.91 (d, J = 8.4 Hz, 1H), 7.81 (d, J = 1.1 Hz, 1H), 7.60 (dd, J = 1.7, 8.3 Hz, 1H), 5.18-4.96 (m, 1H), 2.26 (ddd, J = 2.2, 4.5, 6.5 Hz, 1H), 2.19 (s, 3H), 1.77 (tdd, J = 3.2, 6.8, 19.9 Hz, 1H), 1.33 (tdd, J = 6.3, 9.0, 12.8 Hz, 1H); LCMS(electrospray) m/z 462.1 (M + H+). B (1S,2S)-N-(6-(7-acetamido-5-chloro-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide. 1 TFA 109 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.35-13.37 (m, 1H), 12.79 (s, 1H), 8.07 (d, J = 1.6 Hz, 1H), 7.88 (d, J = 8.3 Hz, 1H), 7.79 (br s, 1H), 7.48 (dd, J = 1.8, 8.3 Hz, 1H), 5.22-4.90 (m, 1H), 2.27-2.19 (m, 4H), 1.83-1.69 (m, 1H), 1.32 (tdd, J = 6.4, 9.0, 12.9 Hz, 1H); LCMS(electrospray) m/z 403.2 (M + H+). B (1S,2S)-N-(6-(6,7-difluoro-5-methyl-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 110 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (br s, 1H), 12.77 (s, 1H), 8.04 (d, J = 1.5 Hz, 1H), 7.84 (d, J = 8.3 Hz, 1H), 7.67 (s, 1H), 7.48 (dd, J = 1.7, 8.3 Hz, 1H), 5.16-4.94 (m, 1H), 2.97 (d, J = 2.1 Hz, 6H), 2.27-2.22 (m, 1H), 2.20 (s, 3H), 1.83-1.69 (m, 1H), 1.39-1.26 (m, 1H); LCMS(electrospray) m/z 460 (M + H+). B (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 111 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.77-13.52 (m, 1H), 12.80 (s, 1H), 8.09 (d, J = 1.5 Hz, 1H), 7.86 (d, J = 8.4 Hz, 1H), 7.78 (s, 1H), 7.52 (dd, J = 1.8, 8.3 Hz, 1H), 5.20-4.93 (m, 1H), 2.55 (s, 3H), 2.30-2.24 (m, 1H), 2.22 (s, 3H), 1.83-1.70 (m, 1H), 1.32 (tdd, J = 6.4, 8.9, 12.8 Hz, 1H); LCMS(electrospray) m/z 462.05 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7- bis(methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 1 TFA 112 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 12.83 (s, 1H), 8.14 (d, J = 1.5 Hz, 1H), 7.92 (d, J = 8.3 Hz, 1H), 7.85 (d, J = 1.2 Hz, 1H), 7.53 (dd, J = 1.7, 8.3 Hz, 1H), 5.19-4.94 (m, 1H), 3.50 (s, 3H), 2.29 (br s, 1H), 2.24 (d, J = 2.9 Hz, 3H), 1.85-1.69 (m, 1H), 1.41-1.24 (m, 1H); LCMS(electrospray) m/z 463.1 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylsulfonyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide 113 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.94-12.86 (m, 1H), 12.83-12.74 (m, 1H), 9.90 (br s, 1H), 8.09 (br s, 1H), 7.88 (br d, J = 7.9 Hz, 1H), 7.66 (br s, 1H), 7.49 (br d, J = 7.4 Hz, 1H), 5.19-4.95 (m, 1H), 2.28-2.23 (m, 1H), 2.20 (br s, 3H), 2.16 (br s, 3H), 1.84-1.69 (m, 1H), 1.42-1.25 (m, 1H); LCMS(electrospray) m/z 442.0 (M + H+). B (1S,2S)-N-(6-(7-acetamido-6-fluoro-5- methyl-1H-indazol-4-yl)benzo[d]thiazol- 2-yl)-2-fluorocyclopropane-1-carboxamide 114 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.05 (s, 1H), 10.78 (s, 1H), 8.08 (s, 1H), 7.83 (d, J = 8.4 Hz, 1H), 7.72 (s, 1H), 7.12 (d, J = 8.0 Hz, 1H), 6.45 (d, J = 12.4 Hz, 1H), 5.14-4.95 (m, 1H), 3.37 (s, 3H), 2.25-2.20 (m, 1H), 1.78-1.68 (m, 1H), 1.34-1.28 (m, 10H); LCMS (electrospray) m/z 549.1 (M + H)+. B tert-butyl 2-(5-chloro-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazol-7-yl)-1-methylhydrazine-1- carboxylate 115 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.88 (s, 1H), 12.79 (s, 1H), 8.25 (s, 1H), 8.11 (s, 1H), 7.89 (d, J = 8.4 Hz, 1H), 7.76 (s, 1H), 7.52 (d, J = 8.0 Hz, 1H), 6.45 (d, J = 12.4 Hz, 1H), 5.13-4.96 (m, 1H), 4.04-3.99 (m, 1H), 3.23 (s, 3H), 2.25-2.20 (m, 1H), 1.78-1.68 (m, 1H), 1.34-1.28 (m, 1H); LCMS (electrospray) m/z 449.1 (M + H)+. B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- methylhydrazineyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 116 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.28 (s, 1H), 12.87-12.78 (m, 1H), 8.14 (d, J = 1.5 Hz, 1H), 7.91 (d, J = 8.3 Hz, 1H), 7.80 (d, J = 1.3 Hz, 1H), 7.53 (dd, J = 1.8, 8.4 Hz, 1H), 5.18-4.95 (m, 1H), 3.98 (s, 3H), 2.21 (d, J = 3.1 Hz, 3H), 1.91-1.88 (m, 1H), 1.69 (br d, J = 2.8 Hz, 1H), 1.34-1.29 (m, 1H); LCMS(electrospray) m/z 443.1(M + H+). B methyl 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-5- methyl-1H-indazole-7-carboxylate. 1 TFA 117 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.07 (br s, 1H), 12.81 (s, 1H), 8.08 (d, J = 1.5 Hz, 1H), 7.86 (d, J = 8.4 Hz, 2H), 7.50 (dd, J = 1.8, 8.3 Hz, 1H), 5.19- 4.94 (m, 1H), 2.29-2.20 (m, 4H), 1.84-1.68 (m, 1H), 1.38-1.26 (m, 1H); LCMS(electrospray) m/z 435.1 (M + H+). B (1S,2S)-N-(6-(6,7-difluoro-5-(methylthio)- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 2,2,2- trifluoroacetate. 1 TFA 118 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.87-13.43 (m, 1H), 12.78 (s, 1H), 8.07 (s, 1H), 7.85 (d, J = 8.4 Hz, 1H), 7.73 (s, 1H), 7.50 (dd, J = 1.3, 8.4 Hz, 1H), 5.21-4.93 (m, 1H), 4.35 (q, J = 7.0 Hz, 2H), 2.30-2.19 (m, 4H), 1.84-1.70 (m, 1H), 1.41 (t, J = 7.0 Hz, 3H), 1.37-1.27 (m, 1H); LCMS(electrospray) m/z 461.2 (M + H+). B (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5- (methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 119 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 12.87 (s, 1H), 8.24 (d, J = 1.6 Hz, 1H), 8.00 (s, 1H), 7.94 (d, J = 8.4 Hz, 1H), 7.62 (dd, J = 1.8, 8.4 Hz, 1H), 5.17-4.95 (m, 1H), 3.56 (s, 3H), 2.29-2.22 (m, 1H), 1.83-1.71 (m, 1H), 1.37-1.29 (m, 1H); LCMS(electrospray) m/z 483 (M + H+). B (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylsulfonyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 120 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.22-11.13 (m, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.95-7.87 (m, 1H), 7.72-7.70 (m, 1H), 6.96-6.93 (m, 1H), 6.92- 6.89 (m, 1H), 5.07-4.81 (m, 1H), 3.21 (s, 3H), 2.30-2.25 (m, 3H), 2.25-2.23 (m, 1H), 2.20-2.09 (m, 1H), 1.79 (s, 3H), 1.74-1.63 (m, 1H), 1.28- 1.09 (m, 1H); LCMS(electrospray) m/z 456.1 (M + H+) B (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(N-methylacetamido)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide. 1 TFA 121 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (br s, 1H), 12.85 (s, 1H), 8.23 (d, J = 1.6 Hz, 1H), 7.94-7.88 (m, 2H), 7.62 (dd, J = 1.8, 8.4 Hz, 1H), 5.21-4.90 (m, 1H), 2.29-2.17 (m, 1H), 1.85-1.62 (m, 1H), 1.42-1.26 (m, 1H); LCMS(electrospray) m/z 449.2 (M + H+). B 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazole-7-carboxylic acid. 1 TFA 122 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.57 (s, 1H), 12.86 (s, 1H), 8.36-8.16 (m, 1H), 7.96-7.91 (m, 2H), 7.63 (dd, J = 1.8, 8.4 Hz, 1H), 5.22-4.90 (m, 1H), 4.00 (s, 3H), 2.30-2.20 (m, 1H), 1.83-1.68 (m, 1H), 1.45-1.21 (m, 1H); LCMS(electrospray) m/z 463.1 (M + H+). B methyl 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazole-7-carboxylate. 1 TFA 123 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.06-13.79 (m, 1H), 12.83 (s, 1H), 8.21 (d, J = 1.6 Hz, 1H), 7.91-7.89 (m, 1H), 7.63 (d, J = 1.7 Hz, 1H), 7.62- 7.59 (m, 1H), 5.15-4.96 (m, 1H), 3.23 (s, 3H), 2.27-2.23 (m, 1H), 1.82 (s, 3H), 1.76-1.69 (m, 1H), 1.36-1.30 (m, 1H); LCMS(electrospray) m/z 476.1 (M + H+). B (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(N- methylacetamido)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 124 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.94 (br s, 1H), 8.10 (d, J = 1.5 Hz, 1H), 7.91(d, J = 8.3 Hz, 1H), 7.68 (s, 1H), 7.51 (dd, J = 1.7, 8.3 Hz, 1H), 5.19- 4.92 (m, 1H), 2.31-2.25 (m, 1H), 2.19 (d, J = 3.1 Hz, 3H), 1.82-1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS(electrospray) m/z 429.1(M + H+). B 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-5- methyl-1H-indazole-7-carboxylic acid 125 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.86-13.55 (m, 1H), 8.21 (d, J = 1.5 Hz, 1H), 7.92 (s, 1H), 7.90 (s, 1H), 7.61 (dd, J = 1.8, 8.4 Hz, 1H), 5.17-4.94 (m, 1H), 3.13 (s, 3H), 2.94 (s, 3H), 2.28-2.22 (m, 1H), 1.81-1.72 (m, 1H), 1.36-1.28 (m, 1H); LCMS(electrospray) m/z 475.9 (M + H+). B 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N,N- dimethyl-1H-indazole-7-carboxamide 126 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.16 (d, J = 1.6 Hz, 1H), 7.95 (d, J = 3.2 Hz, 1H), 7.89 (d, J = 8.3 Hz, 1H), 7.56 (dd, J = 1.8, 8.3 Hz, 1H), 5.18-4.93 (m, 1H), 2.29-2.20 (m, 1H), 1.83-1.70 (m, 1H), 1.32 (tdd, J = 6.4, 9.0, 12.8 Hz, 1H); LCMS(electrospray) m/z 423.1 (M + H+). B (1S,2S)-N-(6-(5-chloro-6,7-difluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 127 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.71-13.47 (s, 1H), 12.98-12.70 (s, 1H), 8.65-8.55 (s, 1H), 8.21 (s, 1H), 7.97-7.88 (m, 1H), 7.85 (s, 1H), 7.63- 7.56 (m, 1H), 5.20-4.91 (m, 1H), 2.91 (br d, J = 4.3 Hz, 3H), 2.30-2.21 (m, 1H), 1.84-1.69 (m, 1H), 1.41-1.28 (m, 1H); LCMS(electrospray) m/z 462.0 (M + H+). B 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N- methyl-1H-indazole-7-carboxamide 128 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69 (s, 1H), 12.86 (s, 1H), 8.24 (d, J = 1.5 Hz, 1H), 7.97-7.87 (m, 2H), 7.63 (dd, J = 1.7, 8.4 Hz, 1H), 5.22-4.92 (m, 1H), 2.77 (d, J = 6.2 Hz, 3H), 2.31-2.21 (m, 1H), 1.83-1.70 (m, 1H), 1.25-1.32 (m, J = 2.5, 6.3, 12.8 Hz, 1H); LCMS(electrospray) m/z 447.2 (M + H+). B (1S,2S)-N-(6-(7-acetyl-5-chloro-6-fluoro- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 129 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.14 (s, 1H), 7.92-7.82 (m, 2H), 7.59-7.51 (m, 1H), 5.18-4.92 (m, 1H), 4.51-4.40 (m, 1H), 4.11-3.85 (m, 3H), 2.94 (s, 3H), 2.89-2.16 (m, 1H), 2.03-1.88 (m, 1H), 1.83-1.68 (m, 1H), 1.38-1.27 (m, 1H); LCMS (electrospray) m/z 489.10 (M + H)+. B (1S,2S)-N-(6-(7-(azetidin-3- yl(methyl)amino)-5-chloro-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 130 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.86-13.56 (m, 1H), 12.93-12.67 (m, 1H), 8.01 (s, 1H), 7.82 (d, J = 8.3 Hz, 1H), 7.63 (s, 1H), 7.40 (br d, J = 8.5 Hz, 1H), 5.20-4.90 (m, 1H), 3.01 (s, 6H), 2.28- 2.18 (m, 1H), 1.82-1.69 (m, 1H), 1.31 (ddd, J = 2.4, 6.4, 12.5 Hz, 1H); LCMS(electrospray) m/z 482.1 (M + H+). B (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-(trifluoromethyl)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 131 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.39 (s, 1H), 12.82 (br d, J = 1.7 Hz, 1H), 8.13 (s, 1H), 7.91 (d, J = 8.3 Hz, 1H), 7.76 (s, 1H), 7.52 (dd, J = 1.4, 8.3 Hz, 1H), 5.18-4.92 (m, 1H), 2.74 (d, J = 6.2 Hz, 3H), 2.24 (br d, J = 3.2 Hz, 3H), 1.86-1.66 (m, 1H), 1.32 (tdd, J = 6.5, 8.8, 12.7 Hz, 1H); LCMS(electrospray) m/z 427.10 (M + H+). B (1S,2S)-N-(6-(7-acetyl-6-fluoro-5-methyl- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 132 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.19 (s, 1H), 12.81 (br s, 1H), 8.11 (d, J = 1.5 Hz, 1H), 7.90 (d, J = 8.3 Hz, 1H), 7.70 (d, J = 1.1 Hz, 1H), 7.50 (dd, J = 1.7, 8.3 Hz, 1H), 5.18-4.93 (m, 1H), 2.90 (d, J = 4.5 Hz, 3H), 2.29-2.24 (m, 1H), 2.22 (d, J = 3.1 Hz, 3H), 1.87-1.67 (m, 1H), 1.33 (tdd, J = 6.4, 8.9, 12.7 Hz, 1H); LCMS(electrospray) m/z 442.1 (M + H+). B 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N,5- dimethyl-1H-indazole-7-carboxamide 133 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (br s, 1H), 12.81 (s, 1H), 8.15 (d, J = 1.5 Hz, 1H), 7.89 (d, J = 8.4 Hz, 1H), 7.78 (s, 1H), 7.57 (dd, J = 1.8, 8.4 Hz, 1H), 5.17-4.92 (m, 1H), 3.26 (q, J = 6.4 Hz, 2H), 2.98 (s, 3H), 2.30-2.21 (m, 1H), 1.85-1.70 (m, 1H), 1.33 (tdd, J = 6.5, 8.8, 12.8 Hz, 1H), 1.09 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 462.1(M + H+). B (1S,2S)-N-(6-(5-chloro-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 134 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (br s, 1H), 8.10 (d J = 1.3 Hz, 1H), 7.88 (d J = 8.3 Hz, 1H), 7.74 (s, 1H), 7.51 (dd, J = 1.8, 8.4 Hz, 1H), 5.18- 4.91 (m, 1H), 3.12 (s, 3H), 2.93 (s, 3H), 2.24 (br d, J = 2.1 Hz, 1H), 2.21 (d, J = 2.8 Hz, 3H), 1.83- 1.67 (m, 1H), 1.31 (ddd, J = 2.8, 6.3, 12.7 Hz, 1H); LCMS(electrospray) m/z 455.9 (M + H+). B 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N,N,5- trimethyl-1H-indazole-7-carboxamide 135 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (s, 1H), 12.85 (s, 1H), 8.21 (d, J = 1.4 Hz, 1H), 8.04 (s, 2H), 7.92 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.60 (dd, J = 1.7, 8.3 Hz, 1H), 5.20-4.94 (m, 1H), 2.32- 2.18 (m, 1H), 1.84-1.69 (m, 1H), 1.29~1.36(m, 1H); LCMS(electrospray) m/z 448.1 (M + H+). B 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-1H- indazole-7-carboxamide 136 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.12 (br s, 1H), 12.76 (br d, J = 12.7 Hz, 1H), 8.00 (s, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.54 (s, 1H), 7.43 (dd, J = 1.6, 8.2 Hz, 1H), 5.21-4.89 (m, 1H), 3.21 (q, J = 6.9 Hz, 2H), 2.94 (s, 3H), 2.55 (br d, J = 7.6 Hz, 2H), 2.28- 2.19 (m, 1H), 1.83-1.68 (m, 1H), 1.37-1.26 (m, 1H), 1.07 (dt, J = 4.0, 7.1 Hz, 6H); LCMS(electrospray) m/z 456.2 (M + H+). B (1S,2S)-N-(6-(5-ethyl-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 137 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.11 (s, 1H), 8.04 (d, J = 1.4 Hz, 1H), 7.85 (d, J = 8.6 Hz, 1H), 7.64 (s, 1H), 7.47 (dd, J = 1.8, 8.3 Hz, 1H), 5.19- 4.89 (m, 1H), 3.23-3.17 (m, 2H), 2.93 (d, J = 1.9 Hz, 3H), 2.28-2.20 (m, 1H), 2.17 (d, J = 3.1 Hz, 3H), 1.85-1.68 (m, 1H), 1.38-1.23 (m, 1H), 1.06 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 441.14 (M + H+). B (1S,2S)-N-(6-(7-(ethyl(methyl)amino)-6- fluoro-5-methyl-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 138 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.34 (br s, 1H), 8.04 (d, J = 1.3 Hz, 1H), 7.83 (d, J = 8.2 Hz, 1H), 7.68 (s, 1H), 7.49 (dd, J = 1.7, 8.3 Hz, 1H), 5.16- 4.94 (m, 1H), 3.23 (q, J = 7.1 Hz, 2H), 2.95 (d, J = 2.0 Hz, 3H), 2.28-2.22 (m, 1H), 2.20 (s, 3H), 1.82- 1.68 (m, 1H), 1.31 (tdd, J = 6.2, 8.9, 12.6 Hz, 1H), 1.07 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 474.1 (M + H+). B (1S,2S)-N-(6-(7-(ethyl(methyl)amino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 139 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31 (s, 1H), 12.77 (s, 1H), 8.33 (s, 1H), 8.24 (br s, 1H), 7.89- 7.81 (m, 1H), 7.80-7.74 (m, 1H), 7.13 (br d, J = 13.7 Hz, 1H), 5.17-4.92 (m, 1H), 2.95 (br s, 6H), 2.27-2.18 (m, 1H), 1.82-1.69 (m, 1H), 1.31 (br s, 1H); LCMS(electrospray) m/z 414.2 (M + H+). B (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)benzo[d]thiazol-2- yl)-2-fluorocyclopropane-1-carboxamide 140 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.04 (br s, 1H), 12.83 (br s, 1H), 8.47-8.36 (m, 2H), 7.92-7.83 (m, 2H), 7.45 (br d, J = 11.7 Hz, 1H), 5.19-4.95 (m, 1H), 2.30-2.20 (m, 1H), 1.84-1.70 (m, 1H), 1.34 (ddd, J = 2.4, 6.2, 12.9 Hz, 1H); LCMS(electrospray) m/z 455.2 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide 141 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56 (s, 1 H) 12.81 (s, 1 H) 8.42 (s, 1 H) 8.34 (s, 1 H) 7.89-7.82 (m, 2 H) 7.29 (d, J = 10.4 Hz, 1 H) 5.14-4.97 (m, 1 H) 2.49 (s, 3 H) 2.28-2.23 (m, 1 H) 1.80-1.73 (m, 1 H) 1.35-1.30 (m, 1 H); LCMS(electrospray) m/z 416.9 (M + H+). B (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- (methylthio)-1H-indazol-4- yl)benzo[d]thiazol-2-yl)cyclopropane-1- carboxamide 142 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.21-13.61 (m, 1 H) 12.76 (s, 1 H) 8.35 (d, J = 1.50 Hz, 1 H) 8.31 (s, 1 H) 7.85-7.89 (m, 1 H) 7.79 (dd, J = 8.38, 1.75 Hz, 1 H) 7.34-7.39 (m, 1 H) 7.27-7.32 (m, 1 H) 4.93-5.17 (m, 1 H) 3.17 (s, 1 H) 2.62 (s, 3 H) 2.20-2.29 (m, 1 H) 1.70-1.82 (m, 1 H) 1.32 (ddt, J = 12.77, 8.93, 6.35, 6.35 Hz, 1 H); LCMS(electrospray) m/z 399.0 (M + H+). B (1S,2S)-2-fluoro-N-(6-(7-(methylthio)-1H- indazol-4-yl)benzo[d]thiazol-2- yl)cyclopropane-1-carboxamide 143 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.77 (br s, 1H), 8.15-7.99 (m, 2H), 7.83 (br d, J = 8.3 Hz, 1H), 7.45 (br d, J = 8.1 Hz, 1H), 7.18 (br s, 1H), 5.17- 4.93 (m, 1H), 2.33 (s, 3H), 2.25 (br s, 1H), 1.84- 1.70 (m, 1H), 1.37-1.27 (m, 1H); LCMS(electrospray) m/z 346.1(M + H+). B (1S,2S)-N-(6-(5-chloro-7-cyano-6-fluoro- 1H-indazol-4-yl)benzo[d]thiazol-2-yl)-2- fluorocyclopropane-1-carboxamide 144 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (br s, 1H), 12.82 (br s, 1H), 8.11 (s, 1H), 7.98 (s, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.55 (td, J = 2.1, 8.3 Hz, 1H), 7.47 (dd, J = 0.7, 9.7 Hz, 1H), 5.18-4.90 (m, 1H), 2.79 (s, 3H), 2.63 (d, J = 1.0 Hz, 3H), 2.24 (td, J = 6.9, 13.6 Hz, 1H), 1.85-1.67 (m, 1H), 1.39-1.25 (m, 1H); LCMS(electrospray) m/z 442.2 (M + H+). B 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N,N- dimethyl-1H-indazole-7-carboxamide 145 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (br s, 1H), 12.82 (br s, 1H), 8.11 (s, 1H), 7.98 (s, 1H), 7.85 (d, J = 8.3 Hz, 1H), 7.55 (td, J = 2.1, 8.3 Hz, 1H), 7.47 (dd, J = 0.7, 9.7 Hz, 1H), 5.18-4.90 (m, 1H), 2.79 (s, 3H), 2.63 (d, J = 1.0 Hz, 3H), 2.24 (td, J = 6.9, 13.6 Hz, 1H), 1.85-1.67 (m, 1H), 1.39-1.25 (m, 1H); LCMS(electrospray) m/z 442.2 (M + H+). B 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)benzo[d]thiazol-6-yl)-N,N- dimethyl-1H-indazole-5-carboxamide 146 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.04 (s, 1H), 12.86 (s, 1H), 8.19 (d, J = 8.8 Hz, 1H), 7.74 (s, 1H), 7.65 (d, J = 8.4 Hz, 1H), 7.48 (d, J = 8.4 Hz, 1H), 7.29 (d, J = 8.4 Hz, 1H), 5.14-4.93 (m, 1H), 2.35 (s, 3H), 2.29-2.20 (m, 1H), 1.77-1.70 (m, 1H), 1.35-1.26 (m, 1H); LCMS (electrospray) m/z 368.1 (M + H)+. D (1S,2S)-2-fluoro-N-(5-(5-methyl-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 147 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.96 (s, 1H), 8.25 (d, J = 8.0 Hz, 1H), 7.80 (s, 1H), 7.71 (d, J = 8.4 Hz, 1H), 7.42 (d, J = 10.0 Hz, 1H), 5.17-4.98 (m, 1H), 2.69 (s, 3H), 2.28-2.21 (m, 1H), 1.81-1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS (electrospray) m/z 386.1 (M + H)+. D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 3 HCl 148 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.10 (br s, 1H), 12.95 (s, 1H), 8.21 (d, J = 8.0 Hz, 1H), 7.53 (d, J = 8.0 Hz, 1H), 7.37 (d, J = 10.1 Hz, 1H), 5.18-4.97 (m, 1H), 2.27 (s, 3H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 432.1 (M + H)+. D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 3-(methylthio)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 3 HCl 149 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.77 (s, 1H), 12.97 (s, 1H), 8.27 (d, J = 8.4 Hz, 1H), 7.93 (s, 1H), 7.82 (d, J = 8.5 Hz, 1H), 5.20-4.95 (m, 1H), 4.40 (q, J = 7.0 Hz, 2H), 2.31-2.23 (m, 1H), 1.85-1.71 (m, 1H), 1.41 (t, J = 6.9 Hz, 3H), 1.38-1.30 (m, 1H); LCMS (electrospray) m/z 450.2 (M + H)+. C (1S,2S)-N-(5-(5-chloro-7-ethoxy-6-fluoro- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 150 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.93 (s, 1 H), 8.25 (d, J = 8.31 Hz, 1 H), 7.64-7.59 (m, 2 H), 7.39 (d, J = 11.62 Hz, 1 H), 5.19-4.96 (m, 1 H), 3.08 (dt, J = 14.15, 7.17 Hz, 1 H), 2.30-2.23 (m, 1 H), 1.83- 1.71 (m, 1 H), 1.40-1.32 (m, 1 H), 1.31-1.23 (m, 6 H); LCMS (electrospray) m/z 414.2 (M + H)+. D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- isopropyl-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 151 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.91 (s, 1 H), 8.25 (d, J = 8.56 Hz, 1 H), 8.00 (s, 1 H), 7.95 (d, J = 8.44 Hz, 1 H), 7.40 (d, J = 10.88 Hz, 1 H), z, 1 H), 5.21-4.94 (m, 1 H), 2.30-2.23 (m, 1 H), 1.84- 1.69 (m, 1 H), 1.41-1.28 (m, 1 H); LCMS (electrospray) m/z 387.2 (M + H)+. D (1S,2S)-N-(5-(5-amino-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 152 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (br s, 1H), 12.94 (br s, 1H), 8.26 (d, J = 8.2 Hz, 1H), 7.72 (s, 1H), 7.68 (d, J = 8.3 Hz, 1H), 7.42 (d, J = 10.1 Hz, 1H), 5.20-4.95 (m, 1H), 2.65 (dq, J = 2.4, 7.2 Hz, 2H), 2.27 (m, 1H), 1.85-1.69 (m, 1H), 1.34 (m, 1H), 1.11 (t, J = 7.0 Hz, 3H); LCMS (electrospray) m/z 400.4 (M + H)+. D (1S,2S)-N-(5-(5-ethyl-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 153 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.99 (s, 1H), 8.29 (d, J = 8.4 Hz, 1H), 7.91 (d, J = 0.9 Hz, 1H), 7.84 (d, J = 8.4 Hz, 1H), 7.71 (dd, J = 0.9, 9.2 Hz, 1H), 5.20-4.96 (m, 1H), 2.31-2.23 (m, 1H), 1.84-1.71 (m, 1H), 1.40-1.31 (m, 1H); LCMS (electrospray) m/z 406.3 (M + H)+. D (1S,2S)-N-(5-(5-chloro-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 154 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 12.96 (s, 1H), 8.26 (d, J = 8.3 Hz, 1H), 7.89 (s, 1H), 7.83 (d, J = 8.3 Hz, 1H), 5.21-4.95 (m, 1H), 3.30 (q, J = 6.4 Hz, 4H), 2.31-2.22 (m, 1H), 1.84-1.71 (m, 1H), 1.41-1.27 (m, 2H), 1.02 (t, J = 7.1 Hz, 6H); LCMS (electrospray) m/z 477.3 (M + H)+. D (1S,2S)-N-(5-(5-chloro-7-(diethylamino)- 6-fluoro-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 155 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6)) δ 12.93 (s, 1H), 8.25 (d, J = 8.6 Hz, 1H), 8.16 (s, 1H), 7.98 (d, J = 8.4 Hz, 1H), 7.55 (d, J = 10.6 Hz, 1H), 5.22-4.93 (m, 1H), 3.73 (s, 3H), 2.31-2.22 (m, 1H), 1.85-1.70 (m, 1H), 1.41-1.28 (m, 1H); LCMS (electrospray) m/z 402.4 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- methoxy-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)cyclopropane-1- carboxamide 156 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.94 (s, 1H), 8.29-8.21 (m, 1H), 7.80 (d, J = 0.8 Hz, 1H), 7.74 (d, J = 8.4 Hz, 1H), 7.55 (dd, J = 0.8, 9.5 Hz, 1H), 5.20-4.95 (m, 1H), 2.32-2.27 (m, 1H), 2.26 (s, 3H), 1.84-1.71 (m, 1H), 1.35 (tdd, J = 6.4, 8.9, 13.0 Hz, 1H); LCMS(electrospray) m/z 418.3 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- (methylthio)-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)cyclopropane-1- carboxamide 157 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.84 (br s, 1H), 13.07 (s, 1H), 8.39-8.30 (m, 2H), 8.08 (d, J = 8.4 Hz, 1H), 7.77 (d, J = 9.5 Hz, 1H), 5.21-4.97 (m, 1H), 2.29 (td, J = 6.9, 13.4 Hz, 1H), 1.86-1.71 (m, 1H), 1.43-1.28 (m, 1H); LCMS(electrospray) m/z 397.4 (M + H+). D (1S,2S)-N-(5-(5-cyano-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 158 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.17 (br s, 1H), 12.83 (br s, 1H), 8.22 (d, J = 8.4 Hz, 1H), 7.87 (s, 1H), 7.81 (d, J = 8.4 Hz, 1H), 7.38 (d, J = 10.2 Hz, 1H), 5.20-4.95 (m, 1H), 2.31-2.23 (m, 1H), 2.07- 1.98 (m, 1H), 1.84-1.69 (m, 1H), 1.34 (tdd, J = 6.4, 8.9, 12.8 Hz, 1H), 0.72-0.61 (m, 2H), 0.17- 0.06 (m, 2H); LCMS(electrospray) m/z 412.4 (M + H+). D (1S,2S)-N-(5-(5-cyclopropyl-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 159 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.93 (s, 1H), 8.21 (d, J = 8.4 Hz, 1H), 7.93 (br s, 1H), 7.78 (d, J = 8.5 Hz, 1H), 5.19-4.96 (m, 1H), 2.31-2.22 (m, 1H), 1.84-1.70 (m, 1H), 1.39-1.27 (m, 1H), 1.22 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 449.3 (M + H+). D (1S,2S)-N-(5-(5-chloro-7-(ethylamino)-6- fluoro-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 160 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.46 (br s, 1H), 12.97 (s, 1H), 8.29 (d, J = 8.3 Hz, 1H), 7.83 (s, 1H), 7.78 (d, J = 8.4 Hz, 1H), 7.67 (d, J = 8.8 Hz, 1H), 5.20-4.96 (m, 1H), 2.31-2.23 (m, 1H), 1.84-1.71 (m, 1H), 1.35 (tdd, J = 6.4, 9.0, 13.0 Hz, 1H); LCMS(electrospray) m/z 452.0 (M + H+). D (1S,2S)-N-(5-(5-bromo-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 161 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.91 (s, 1H), 8.23 (d, J = 8.4 Hz, 1H), 7.72 (s, 1H), 7.64 (d, J = 8.4 Hz, 1H), 5.24-4.90 (m, 1H), 2.99 (s, 3H), 2.98 (s, 3H), 2.70-2.58 (m, 2H), 2.31-2.21 (m, 1H), 1.86- 1.67 (m, 1H), 1.41-1.26 (m, 1H), 1.12 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 443.2 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-5-ethyl- 6-fluoro-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 162 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 12.95 (s, 1H), 8.27 (d, J = 8.4 Hz, 1H), 7.79 (s, 1H), 7.69 (d J = 8.3 Hz, 1H), 5.18-4.96 (m, 1H), 2.67- 2.64 (m, 2H), 2.53 (br s, 3H), 2.30-2.22 (m, 1H), 1.82-1.71 (m, 1H), 1.35 (tdd, J = 6.5, 8.8, 12.9 Hz, 1H), 1.12 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 446.3 (M + H+). D (1S,2S)-N-(5-(5-ethyl-6-fluoro-7- (methylthio)-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 163 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 13.46 (br s, 1H), 12.98 (s, 1H), 8.27 (d, J = 8.4 Hz, 1H), 7.88 (s, 1H), 7.73 (d, J = 8.4 Hz, 1H), 5.24-4.95 (m, 1H), 3.51 (br t, J = 6.9 Hz, 3H), 3.03 (br t, J = 6.6 Hz, 2H), 2.28 (br d, J = 2.6 Hz, 4H), 1.84-1.71 (m, 1H), 1.80-1.30 (m, 1H), 1.41-1.30 (m, 1H); LCMS(electrospray) m/z 462.1 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2- hydroxyethyl)thio)-5-methyl-1H-indazol- 4-yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 2TFA 164 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.65 (br s, 1H), 13.02 (s, 1H), 8.30 (d, J = 8.4 Hz, 1H), 8.10 (s, 1H), 7.92 (d, J = 8.4 Hz, 1H), 7.67 (d, J = 11.2 Hz, 1H), 5.19-4.97 (m, 1H), 3.18 (d, J = 1.0 Hz, 3H), 2.31- 2.25 (m, 1H), 1.84-1.71 (m, 1H), 1.41-1.29 (m, 1H); LCMS(electrospray) m/z 434 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- (methylsulfinyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 165 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52 (br s, 1H), 13.33 (br s, 1H), 12.97 (s, 1H), 8.28 (d, J = 8.4 Hz, 1H), 8.09 (s, 1H), 7.81 (s, 1H), 7.71 (br s, 1H), 7.68 (d, J = 8.4 Hz, 1H), 5.25-4.96 (m, 1H), 3.97 (q, J = 7.1 Hz, 2H), 3.93-3.87 (m, 1H), 3.78 (s, 2H), 3.70 (s, 1H), 2.72-2.62 (m, 3H), 2.32-2.23 (m, 1H), 1.84-1.71 (m, 1H), 1.41-1.31 (m, 1H), 1.21 (t, J = 7.5 Hz, 1H), 1.12 (t, J = 7.4 Hz, 3H), 1.01 (t, J = 7.1 Hz, 3H), 0.94 (t, J = 7.1 Hz, 1H); LCMS(electrospray) m/z 518.3 (M + H+). D ethyl 2-((5-ethyl-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 1H-indazol-7-yl)thio)acetate. 2 TFA 166 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (s, 1H), 8.10 (d, J = 8.2 Hz, 1H), 7.81 (s, 1H), 7.58 (d, J = 8.2 Hz, 1H), 5.19-4.84 (m, 1H), 3.97 (s, 2H), 3.02 (s, 3H), 2.91-2.76 (m, 6H), 2.74-2.62 (m, 2H), 2.21-2.10 (m, 1H), 1.81-1.64(m, 1H), 1.29-1.19 (m, 1H), 1.13 (t, J = 7.3 Hz, 3H); LCMS(electrospray) m/z 517.1 (M + H+). D (1S,2S)-N-(5-(7-((2-(dimethylamino)-2- oxoethyl)thio)-5-ethyl-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 167 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.82 (d, J = 7.9 Hz, 1H), 7.72 (s, 1H), 7.41 (d, J = 8.2 Hz, 1H), 5.03- 4.68 (m, 1H), 3.18 (s, 1H), 2.86 (s, 1H), 2.70- 2.63 (m, 2H), 2.01-1.91 (m, 1H), 1.72-1.57 (m, 1H), 1.12 (t, J = 7.3 Hz, 3H), 1.05-0.96 (m, 1H); LCMS(electrospray) m/z 503.3 (M + H+). D (1S,2S)-N-(5-(5-ethyl-6-fluoro-7-((2- (methylamino)-2-oxoethyl)thio)-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 168 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 7.82 (d, J = 7.9 Hz, 1H), 7.72 (s, 1H), 7.41 (d, J = 8.2 Hz, 1H), 5.03- 4.68 (m, 1H), 3.18 (s, 1H), 2.86 (s, 1H), 2.70- 2.63 (m, 2H), 2.01-1.91 (m, 1H), 1.72-1.57 (m, 1H), 1.12 (t, J = 7.3 Hz, 3H), 1.05-0.96 (m, 1H); LCMS(electrospray) m/z 490.3 (M + H+). D 2-((5-ethyl-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 1H-indazol-7-yl)thio)acetic acid 169 05embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 8.15 (d, J = 8.3 Hz, 1H), 7.89 (br s, 1H), 7.60 (d, J = 8.3 Hz, 1H), 5.10-4.76 (m, 1H), 3.13 (d, J = 1.6 Hz, 6H), 2.35 (d, J = 3.4 Hz, 3H), 2.12-2.01 (m, 2H), 1.49- 1.33 (m, 1H); LCMS(electrospray) m/z429.1 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-methyl-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 170 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.65 (s, 1H), 12.94 (br s, 1H), 8.25 (d, J = 8.4 Hz, 1H), 7.89- 7.84 (m, 1H), 7.75 (d, J = 8.3 Hz, 1H), 5.20-4.94 (m, 1H), 2.56 (s, 3H), 2.28 (s, 3H), 2.27-2.23 (m, 1H), 1.84-1.72 (m, 1H), 1.41-1.30 (m, 1H); LCMS(electrospray) m/z 464.0 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5,7- bis(methylthio)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 171 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.96 (s, 1H), 12.92 (s, 1H), 8.41 (d, J = 6.5 Hz, 1H), 8.38 (d, J = 1.2 Hz, 1H), 8.29 (d, J = 8.6 Hz, 1H), 8.15 (d, J = 7.7 Hz, 1H), 5.21-4.94 (m, 1H), 2.24 (s, 1H), 1.88- 1.69 (m, 1H), 1.41-1.29 (m, 1H); LCMS(electrospray) m/z 0.887, 440.1 (M + H+). D (1S,2S)-2-fluoro-N-(5-(5-fluoro-6- (trifluoromethyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. TFA 172 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56-13.42 (m, 1H), 8.24 (d, J = 8.4 Hz, 1H), 7.90 (br s, 1H), 7.79 (d, J = 8.4 Hz, 1H), 5.20-4.95 (m, 1H), 3.02 (br d, J = 1.7 Hz, 6H), 2.27 (ddd, J = 2.0, 4.6, 6.7 Hz, 1H), 1.85-1.71 (m, 1H), 1.38-1.30 (m, 1H), 1.30 (s, 1H); LCMS(electrospray) m/z 449.1 (M + H+). D (1S,2S)-N-(5-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 173 09embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.57-13.32 (m, 1H), 8.25 (dd, J = 3.0, 8.3 Hz, 1H), 7.86 (br s, 1H), 7.70 (dd, J = 2.9, 8.3 Hz, 1H), 5.22-4.91 (m, 1H), 2.53 (br s, 3H), 2.27 (br s, 3H), 1.83-1.70 (m, 1H), 1.40-1.27 (m, 1H), 1.21 (br d, J = 10.5 Hz, 2H); LCMS(electrospray) m/z 431.07 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 174 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (s, 1H), 12.98 (s, 1H), 8.29 (d, J = 8.4 Hz, 1H), 7.98 (d, J = 1.3 Hz, 1H), 7.85 (d, J = 8.4 Hz, 1H), 5.21-4.96 (m, 1H), 2.58 (s, 3H), 2.31-2.25 (m, 1H), 1.84- 1.72 (m, 1H), 1.37-1.30 (m, 1H); LCMS(electrospray) m/z 452 (M + H+). D (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylthio)-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 175 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54-13.33 (m, 1H), 12.92 (s, 1H), 8.23 (d, J = 8.3 Hz, 1H), 7.82 (s, 1H), 7.68 (d, J = 8.3 Hz, 1H), 5.19-4.96 (m, 1H), 4.33 (q, J = 7.0 Hz, 2H), 2.30-2.25 (m, 4H), 1.83-1.72 (m, 1H), 1.39 (t, J = 7.0 Hz, 3H), 1.36-1.32 (m, 1H); LCMS(electrospray) m/z 430.2 (M + H+). D (1S,2S)-N-(5-(7-ethoxy-6-fluoro-5- methyl-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 176 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.90-13.81 (m, 1H), 12.94 (br s, 1H), 8.26 (d, J = 8.4 Hz, 1H), 7.87-7.80 (m, 1H), 7.67 (d, J = 8.3 Hz, 1H), 5.17- 4.95 (m, 1H), 2.76-2.68 (m, 2H), 2.27-2.19 (m, 1H), 1.82-1.73 (m, 1H), 1.57-1.42 (m, 1H), 1.15- 1.11 (m, 3H); LCMS(electrospray) m/z 418 (M + H+). D (1S,2S)-N-(5-(5-ethyl-6,7-difluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 177 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (s, 1H), 12.97 (s, 1H), 8.29 (d, J = 8.3 Hz, 1H), 7.92 (s, 1H), 7.74 (d, J = 8.3 Hz, 1H), 5.20-4.96 (m, 1H), 3.14 (s, 3H), 2.31-2.23 (m, 4H), 1.84-1.71 (m, 1H), 1.35 (tdd, J = 6.4, 8.9, 13.0 Hz, 1H); LCMS(electrospray) m/z 447.9 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylsulfinyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 178 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (s, 1H), 12.93 (s, 1H), 8.25 (d, J = 8.0 Hz, 1H), 7.76 (s, 1H), 7.67-7.65 (m, 1H), 5.21-4.96 (m, 1H), 4.37-4.31 (m, 2H), 2.68-2.64 (m, 2H), 2.34-2.33 (m, 1H), 1.81-1.68 (m, 1H), 1.40 (t, J = 6.8 Hz, 3H), 1.19- 1.15 (m, 1H), 1.13 (t, J = 7.6 Hz, 3H); LCMS(electrospray) m/z 444.2 (M + H+). D (1S,2S)-N-(5-(7-ethoxy-5-ethyl-6-fluoro- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 1 TFA 179 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27 (br s, 1H), 12.97 (s, 1H), 10.16 (s, 1H), 8.29 (d, J = 8.4 Hz, 1H), 7.91 (s, 1H), 7.85 (d, J = 8.3 Hz, 1H), 5.18- 4.98 (m, 1H), 2.28 (ddd, J = 2.4, 4.3, 6.6 Hz, 1H), 2.19 (s, 3H), 1.82-1.73 (m, 1H), 1.35 (ddd, J = 2.6, 6.3, 12.9 Hz, 1H); LCMS(electrospray) m/z 463.1(M + H+). D (1S,2S)-N-(5-(7-acetamido-5-chloro-6- fluoro-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 180 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68 (br s, 1H), 13.02 (s, 1H), 8.32 (d, J = 8.4 Hz, 1H), 8.05 (br s, 1H), 7.87 (d, J = 8.4 Hz, 1H), 5.20-4.98 (m, 1H), 3.19 (s, 3H), 2.31-2.25 (m, 1H), 1.85-1.71 (m, 1H), 1.36 (tdd, J = 6.6, 8.8, 13.0 Hz, 1H); LCMS(electrospray) m/z 468 (M + H+). D (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylsulfinyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 181 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.96-12.91 (m, 2H), 9.96 (s, 1H), 8.26 (d, J = 8.4 Hz, 1H), 7.79 (s, 1H), 7.71 (d, J = 8.3 Hz, 1H), 5.20-4.94 (m, 1H), 2.27 (d, J = 2.9 Hz, 3H), 2.17 (s, 4H), 1.84- 1.71 (m, 1H), 1.42-1.30 (m, 1H); LCMS(electrospray) m/z 442.10 (M + H+). D (1S,2S)-N-(5-(7-acetamido-6-fluoro-5- methyl-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 182 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.19 (s, 1H), 12.99 (s, 1H), 8.31 (d, J = 8.4 Hz, 1H), 7.97 (s, 1H), 7.76 (d, J = 8.3 Hz, 1H), 5.21-4.95 (m, 1H), 3.51 (s, 3H), 2.33-2.25 (m, 4H), 1.85-1.71 (m, 1H), 1.41-1.28 (m, 1H); LCMS(electrospray) m/z 463.06 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylsulfonyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 183 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44-13.24 (m, 1H), 12.99 (s, 1H), 8.30 (d, J = 8.3 Hz, 1H), 7.98-7.86 (m, 1H), 7.76 (d, J = 8.4 Hz, 1H), 5.27- 4.90 (m, 1H), 3.99 (s, 3H), 2.31-2.24 (m, 4H), 1.82-1.70 (m, 1H), 1.44-1.27 (m, 1H); LCMS(electrospray) m/z 444.0 (M + H+). D methyl 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 5-methyl-1H-indazole-7-carboxylate. 1 TFA 184 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.83-13.51 (m, 1H), 12.93 (s, 1H), 8.23 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.73 (d, J = 8.4 Hz, 1H), 5.22-4.93 (m, 1H), 4.51-4.26 (m, 2H), 2.30-2.28 (m, 1H), 2.06-2.03 (m, 1H), 1.86-1.73 (m, 1H), 1.64-1.52 (m, 1H), 1.42 (t, J = 7.0 Hz, 3H), 1.33 (m, J = 6.7, 14.0 Hz, 1H); LCMS(electrospray) m/z 462.2 (M + H+). D (1S,2S)-N-(5-(7-ethoxy-6-fluoro-5- (methylthio)-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 185 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (s, 1H), 13.03 (s, 1H), 8.34 (d, J = 8.3 Hz, 1H), 8.09 (d, J = 1.3 Hz, 1H), 7.89 (d, J = 8.3 Hz, 1H), 5.20-4.98 (m, 1H), 3.57 (s, 3H), 2.31-2.25 (m, 1H), 1.85- 1.73 (m, 1H), 1.41-1.31 (m, 1H); LCMS(electrospray) m/z 484 (M + H+). D (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylsulfonyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 186 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.92-13.91 (m, 1H), 13.91-13.90 (m, 1H), 13.86 (br s, 1H), 8.23 (d, J = 8.3 Hz, 1H), 7.93 (br d, J = 2.7 Hz, 1H), 7.68 (d, J = 8.3 Hz, 1H), 5.17-4.95 (m, 1H), 2.32- 2.31 (m, 1H), 2.31 (d, J = 2.9 Hz, 2H), 2.26 (dt, J = 2.2, 4.5 Hz, 1H), 1.84-1.73 (m, 1H), 1.32-1.25 (m, 1H); LCMS(electrospray) m/z 404.2 (M + H+). D (1S,2S)-N-(5-(6,7-difluoro-5-methyl-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 1 TFA 187 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.42 (d, J = 8.3 Hz, 1H), 8.14 (d, J = 3.2 Hz, 1H), 7.91 (d, J = 8.4 Hz, 1H), 5.38-5.15 (m, 1H), 2.71-2.70 (m, 3H), 2.45 (br s, 1H), 2.03-1.89 (m, 1H), 1.41 (s, 1H); LCMS(electrospray) m/z 436.1 (M + H+). D (1S,2S)-N-(5-(6,7-difluoro-5-(methylthio)- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 188 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.25 (d, J = 8.4 Hz, 1H), 7.84 (s, 1H), 7.71 (d, J = 8.3 Hz, 1H), 5.04 (dt, J = 3.9, 6.2 Hz, 1H), 2.32 (d, J = 3.3 Hz, 3H), 2.24-2.16 (m, 1H), 1.98-1.84 (m, 1H), 1.34-1.29 (m, 1H); LCMS(electrospray) m/z 429.9 (M + H+). D 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 5-methyl-1H-indazole-7-carboxylic acid. 1 TFA 189 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.34 (s, 1H), 8.31-8.28 (m, 1H), 8.05 (s, 1H), 7.88 (d, J = 8.4 Hz, 1H), 5.17-4.98 (m, 1H), 3.25 (s, 3H), 2.28 (ddd, J = 1.8, 4.7, 6.8 Hz, 1H), 1.83 (s, 3H), 1.75 (dt, J = 3.8, 6.9 Hz, 1H), 1.38-1.32 (m, 1H); LCMS(electrospray) m/z 477.0 (M + H+). D (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(N- methylacetamido)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 190 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.61 (br s, 1H), 12.99-12.91 (m, 1H), 8.31-8.24 (m, 1H), 7.94- 7.88 (m, 1H), 7.77-7.70 (m, 1H), 5.23-4.96 (m, 1H), 3.22 (s, 3H), 2.30 (d, J = 2.8 Hz, 3H), 2.28- 2.23 (m, 1H), 1.80 (s, 3H), 1.77-1.70 (m, 1H), 1.41-1.29 (m, 1H); LCMS(electrospray) m/z 456.12 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(N-methylacetamido)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 191 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.90 (br, 2H), 8.20 (d, J = 8.0 Hz, 1H), 7.83 (s, 1H), 7.76 (d, J = 8.4 Hz, 1H), 7.49 (s, 1H), 5.15-4.98 (m, 1H), 5.04 (d, J = 5.2 Hz, 1H), 3.24 (s, 3H), 2.32-2.26 (m, 2H), 1.80-1.73 (m, 1H), 1.35-1.23 (m, 1H); LCMS (electrospray) m/z 450.1 (M + H)+. D (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(2- methylhydrazineyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 192 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.94 (s, 1H), 12.88 (s, 1H), 8.37 (s, 1H), 8.22 (d, J = 8.4 Hz, 1H), 7.90 (s, 1H), 7.77 (d, J = 8.4 Hz, 1H), 5.15-4.98 (m, 1H), 2.60 (d, J = 5.2 Hz, 3H), 2.18-2.13 (m, 1H), 1.71-1.63 (m, 1H), 1.35-1.12 (m, 10H); LCMS (electrospray) m/z 550.1 (M + H)+. D tert-butyl 2-(5-chloro-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 1H-indazol-7-yl)-1-methylhydrazine-1- carboxylate 193 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.87-13.62 (m, 1H), 8.29 (d, J = 8.5 Hz, 1H), 7.98 (s, 1H), 7.86 (d, J = 8.5 Hz, 1H), 5.18-4.95 (m, 1H), 3.12 (s, 3H), 2.93 (s, 3H), 2.27 (ddd, J = 2.0, 4.6, 6.7 Hz, 1H), 1.82-1.71 (m, 1H), 1.34 (ddd, J = 2.6, 6.3, 13.0 Hz, 1H); LCMS(electrospray) m/z 476.9 (M + H+). D 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- N,N-dimethyl-1H-indazole-7-carboxamide 194 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (br s, 1H), 12.90 (br s, 1H), 8.21 (d, J = 8.8 Hz, 1H), 7.77 (s, 1H), 7.70 (d, J = 8.4 Hz, 1H), 5.19-4.95 (m, 1H), 2.99 (s, 6H), 2.27 (s, 4H), 1.84-1.70 (m, 1H), 1.40- 1.28 (m, 1H); LCMS(electrospray) m/z 461 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 195 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.65 (br d, J = 3.3 Hz, 1H), 8.19-8.12 (m, 1H), 7.95 (s, 1H), 7.77 (d, J = 8.3 Hz, 1H), 5.17-4.89 (m, 1H), 2.91 (d, J = 4.5 Hz, 3H), 2.23-2.14 (m, 1H), 1.85-1.63 (m, 1H), 1.35-1.17 (m, 1H); LCMS(electrospray) m/z 462.9 (M + H+). D 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- N-methyl-1H-indazole-7-carboxamide 196 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53-13.38 (m, 1H), 13.59-13.37 (m, 1H), 8.31-8.23 (m, 1H), 7.96-7.87 (m, 1H), 7.85-7.76 (m, 1H), 5.21- 4.96 (m, 1H), 3.31 (br s, 2H), 3.09-2.92 (m, 3H), 2.35-2.23 (m, 1H), 1.87-1.72 (m, 1H), 1.42-1.30 (m, 1H), 1.14-1.05 (m, 3H); LCMS(electrospray) m/z 463.7 (M + H+). D (1S,2S)-N-(5-(5-chloro-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 197 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48-13.33 (m, 1H), 8.24 (d, J = 8.4 Hz, 1H), 7.86 (s, 1H), 7.72 (d, J = 8.4 Hz, 1H), 5.19-4.93 (m, 1H), 3.12 (s, 3H), 2.92 (s, 3H), 2.28 (d, J = 2.9 Hz, 3H), 2.27- 2.22 (m, 1H), 1.82-1.69 (m, 1H), 1.39-1.28 (m, 1H); LCMS(electrospray) m/z 457.1 (M + H+). D 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- N,N,5-trimethyl-1H-indazole-7- carboxamide 198 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.35 (s, 1H), 8.22 (d, J = 8.4 Hz, 1H), 7.96 (s, 1H), 7.65 (d, J = 8.4 Hz, 1H), 5.17-4.91 (m, 1H), 2.30-2.19 (m, 1H), 1.83-1.69 (m, 1H), 1.39-1.28 (m, 1H); LCMS(electrospray) m/z 474.1 (M + H+). D (1S,2S)-N-(5-(7-chloro-6-fluoro-5- (trifluoromethyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 199 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.01-12.83 (m, 1H), 8.30-8.14 (m, 1H), 7.98-7.94 (m, 1H), 7.80 (s, 1H), 7.71-7.59 (m, 1H), 5.28-4.88 (m, 1H), 2.49-2.48 (m, 3H), 2.27-2.24 (m, 4H), 1.83- 1.72 (m, 1H), 1.39-1.30 (m, 1H); LCMS(electrospray) m/z 400.0 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5,7- dimethyl-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)cyclopropane-1- carboxamide. 1 TFA 200 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 13.03-12.78 (m, 1H), 8.23 (d, J = 8.4 Hz, 1H), 7.74-7.61 (m, 2H), 5.20-4.94 (m, 1H), 3.23 (br d, J = 7.1 Hz, 2H), 2.95 (d, J = 1.8 Hz, 3H), 2.63 (br d, J = 5.8 Hz, 2H), 2.29-2.24 (m, 1H), 1.83- 1.71 (m, 1H), 1.40-1.29 (m, 1H), 1.12 (t, J = 7.4 Hz, 3H), 1.06 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 457.0 (M + H+). D (1S,2S)-N-(5-(5-ethyl-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 201 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.19 (br s, 1H), 12.89 (br s, 1H), 8.24 (d, J = 8.5 Hz, 1H), 8.15 (s, 1H), 8.01 (d, J = 8.5 Hz, 1H), 7.53 (d, J = 10.5 Hz, 1H), 5.19-4.96 (m, 1H), 3.91 (q, J = 7.0 Hz, 2H), 2.31-2.23 (m, 1H), 1.84-1.72 (m, 1H), 1.39-1.30 (m, 1H), 1.15 (t, J = 6.9 Hz, 3H); LCMS(electrospray) m/z 416.0 (M + H+). D (1S,2S)-N-(5-(5-ethoxy-6-fluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 202 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.20-13.00 (m, 1H), 12.95-12.86 (m, 1H), 8.23 (d, J = 8.3 Hz, 1H), 7.80 (s, 1H), 7.67 (d, J = 8.4 Hz, 1H), 6.98- 6.89 (m, 1H), 5.21-4.94 (m, 1H), 4.09 (br t, J = 5.9 Hz, 2H), 3.38-3.33 (m, 2H), 3.04-2.98 (m, 3H), 2.57-2.52 (m, 3H), 2.28 (br dd, J = 2.1, 4.4 Hz, 1H), 2.26-2.26 (m, 1H), 2.25 (d, J = 3.1 Hz, 3H), 1.83-1.71 (m, 1H), 1.39-1.30 (m, 1H); LCMS(electrospray) m/z 516.1 (M + H+). D 2-((6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- 5-methyl-1H-indazol-7- yl)(methyl)amino)ethyl methylcarbamate 203 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.13 (s, 1H), 8.23 (d, J = 8.3 Hz, 1H), 7.77 (s, 1H), 7.68 (d, J = 8.3 Hz, 1H), 5.23-4.94 (m, 1H), 3.22 (q, J = 6.9 Hz, 2H), 2.95 (d, J = 2.1 Hz, 3H), 2.30-2.27 (m, 1H), 2.25 (d, J = 3.2 Hz, 3H), 1.87-1.68 (m, 1H), 1.35 (tdd, J = 6.5, 8.7, 13.1 Hz, 1H), 1.06 (t, J = 7.2 Hz, 3H); LCMS(electrospray) m/z 442.14 (M + H+). D (1S,2S)-N-(5-(7-(ethyl(methyl)amino)-6- fluoro-5-methyl-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 204 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27-13.06 (m, 1H), 8.21 (br d, J = 8.1 Hz, 1H), 7.78 (br s, 1H), 7.66 (br d, J = 8.4 Hz, 1H), 5.19-4.95 (m, 1H), 4.91 (br s, 1H), 3.65-3.55 (m, 2H), 3.27-3.14 (m, 2H), 3.04-2.94 (m, 3H), 2.28-2.19 (m, 4H), 1.82- 1.68 (m, 1H), 1.38-1.26 (m, 1H); LCMS(electrospray) m/z 459.1 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2- hydroxyethyl)(methyl)amino)-5-methyl- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 205 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63 (br s, 1H), 8.27 (d, J = 8.3 Hz, 1H), 7.99 (s, 1H), 7.74 (d, J = 8.3 Hz, 1H), 5.19-4.95 (m, 1H), 2.29 (d, J = 2.9 Hz, 3H), 2.28-2.22 (m, 1H), 1.84-1.70 (m, 1H), 1.39- 1.27 (m, 1H); LCMS(electrospray) m/z 454.2 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(trifluoromethyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 206 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.24 (br d, J = 2.9 Hz, 1H), 8.50-8.44 (m, 1H), 8.18 (d, J = 8.3 Hz, 1H), 7.84 (s, 1H), 7.67 (d, J = 8.2 Hz, 1H), 5.17- 4.89 (m, 1H), 2.91 (d, J = 4.4 Hz, 3H), 2.29 (d, J = 2.8 Hz, 3H), 2.24-2.18 (m, 1H), 1.83-1.67 (m, 1H), 1.35-1.21 (m, 1H); LCMS(electrospray) m/z 442.10 (M + H+). D 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)thiazolo[5,4-b]pyridin-5-yl)- N,5-dimethyl-1H-indazole-7-carboxamide 207 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.86-13.56 (m, 1H), 12.95 (s, 1H), 8.24 (d, J = 8.3 Hz, 1H), 7.73 (s, 1H), 7.62 (d, J = 8.3 Hz, 1H), 5.19-4.96 (m, 1H), 3.03 (d, J = 2.2 Hz, 6H), 2.32-2.21 (m, 1H), 1.83-1.71 (m, 1H), 1.41-1.31 (m, 1H); LCMS(electrospray) m/z 483.2 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-(trifluoromethyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 208 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.23 (d, J = 8.4 Hz, 1H), 7.98 (d, J = 3.3 Hz, 1H), 7.82 (d, J = 8.4 Hz, 1H), 5.04 (dt, J = 3.9, 6.2 Hz, 1H), 2.20 (dtd, J = 4.3, 6.9, 9.1 Hz, 1H), 1.95-1.84 (m, 1H), 1.37-1.29 (m, 1H); LCMS(electrospray) m/z 424.1 (M + H+). D (1S,2S)-N-(5-(5-chloro-6,7-difluoro-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 2,2,2-trifluoroacetate. 1 TFA 209 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 1.27-1.40 (m, 1 H), 1.71-1.83 (m, 1 H), 2.27 (br s, 1 H), 4.95-5.19 (m, 1 H), 7.51 (s, 1 H), 7.65 (s, 1 H), 7.78 (br s, 1 H), 7.87 (br d, J = 8.68 Hz, 1 H), 8.05 (br s, 1 H), 8.21-8.38 (m, 1 H), 12.77-13.42 (m, 1 H), 13.77- 14.05 (m, 1 H); LCMS(electrospray) m/z 456.1 (M + H+). D (1S,2S)-N-(5-(5-chloro-7- (difluoromethyl)-6-fluoro-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 210 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 1.12 (br t, J = 7.40 Hz, 3 H), 1.27-1.42 (m, 1 H), 1.68-1.85 (m, 1 H), 2.22-2.31 (m, 1 H), 2.68 (br d, J = 7.28 Hz, 2 H), 4.90-5.23 (m, 1 H), 7.73 (d, J = 8.41 Hz, 1 H), 7.93 (br s, 1 H), 8.30 (d, J = 8.28 Hz, 1 H), 12.60-13.33 (m, 1 H), 13.48-13.91 (m, 1 H); LCMS(electrospray) m/z 468.2 (M + H+). D (1S,2S)-N-(5-(5-ethyl-6-fluoro-7- (trifluoromethyl)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 211 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.79-13.40 (m, 1H), 13.10-12.67 (m, 1H), 8.75-8.46 (m, 1H), 8.39-8.10 (m, 1H), 8.01-7.71 (m, 1H), 5.24- 4.92 (m, 1H), 2.65-2.55 (m, 3H), 2.32-2.22 (m, 1H), 2.35-2.22 (m, 2H), 1.88-1.63 (m, 1H), 1.49- 1.19 (m, 2H); LCMS(electrospray) m/z 420.0 (M + H+). D (1S,2S)-N-(5-(5-chloro-6-fluoro-7-methyl- 1H-indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 212 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15-13.72 (m, 1 H) 12.88 (s, 1 H) 8.74 (s, 1 H) 8.13-8.21 (m, 2 H) 7.77 (d, J = 7.75 Hz, 1 H) 7.35 (d, J = 7.75 Hz, 1 H) 4.92-5.19 (m, 1 H) 3.17 (s, 1 H) 2.65 (s, 3 H) 2.23-2.31 (m, 1H) 1.74-1.84 (m, 2 H) 1.31-1.39 (m, 1 H); LCMS(electrospray) m/z 400.0 (M + H+). D (1S,2S)-2-fluoro-N-(5-(7-(methylthio)-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 213 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.93 (s, 1H), 8.26 (d, J = 8.4 Hz, 1H), 7.96 (s, 1H), 7.74 (d, J = 8.3 Hz, 1H), 5.25-4.89 (m, 1H), 2.31 (d, J = 2.8 Hz, 3H), 2.29-2.22 (m, 1H), 1.84-1.70 (m, 1H), 1.29-1.36 (m, J = 2.6, 6.2, 12.8 Hz, 1H); LCMS(electrospray) m/z 470.2 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(trifluoromethoxy)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 214 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27 (br s, 1H), 13.01-12.74 (m, 1H), 8.68 (br s, 1H), 8.55 (d, J = 8.6 Hz, 1H), 8.22 (d, J = 8.5 Hz, 1H), 8.15 (q, J = 8.6 Hz, 2H), 7.61 (d, J = 14.3 Hz, 1H), 5.18-4.96 (m, 1H), 2.99 (br s, 6H), 2.30-2.23 (m, 1H), 1.83- 1.72 (m, 1H), 1.38-1.31 (m, 1H); LCMS(electrospray) m/z 415.2 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)thiazolo[5,4- b]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 215 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.03 (s, 1H), 12.97 (s, 1H), 8.82 (s, 1H), 8.26 (s, 2H), 7.90 (d, J = 12.0 Hz, 1H), 5.24-4.94 (m, 1H), 2.28 (ddd, J = 2.0, 4.6, 6.7 Hz, 1H), 1.87-1.70 (m, 1H), 1.32- 1.36 (m, J = 2.6, 6.2, 12.7 Hz, 1H); LCMS(electrospray) m/z 456.2 (M + H+). D (1S,2S)-2-fluoro-N-(5-(6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2- yl)cyclopropane-1-carboxamide 216 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30-12.94 (m, 1H), 8.73-8.65 (m, 1H), 8.15-8.08 (m, 1H), 8.07-8.01 (m, 1H), 7.66 (d, J = 7.9 Hz, 1H), 6.82- 6.73 (m, 1H), 5.29-4.92 (m, 1H), 3.13-2.82 (m, 6H), 2.29-2.18 (m, 1H), 2.07 (s, 1H), 1.84-1.69 (m, 1H), 1.39-1.25 (m, 1H); LCMS(electrospray) m/z 397.1 (M + H+). D (1S,2S)-N-(5-(7-(dimethylamino)-1H- indazol-4-yl)thiazolo[5,4-b]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 217 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94-13.07 (m, 1H), 8.24 (d, J = 8.3 Hz, 1H), 7.92 (s, 1H), 7.74- 7.44 (m, 2H), 5.18-4.91 (m, 1H), 2.27 (d, J = 2.6 Hz, 3H), 2.26-2.22 (m, 1H), 1.82-1.71 (m, 1H), 1.37-1.28 (m, 1H); LCMS(electrospray) m/z 436.1 (M + H+). D (1S,2S)-N-(5-(7-(difluoromethyl)-6- fluoro-5-methyl-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 218 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.33 (br s, 1H), 8.19 (d, J = 8.4 Hz, 1H), 7.77 (s, 1H), 7.70 (d, J = 8.4 Hz, 1H), 5.19-4.95 (m, 1H), 3.25 (br d, J = 7.7 Hz, 2H), 2.97 (d, J = 1.6 Hz, 3H), 2.26 (s, 3H), 1.85- 1.70 (m, 1H), 1.40-1.21 (m, 2H), 1.10-1.04 (m, 3H); LCMS(electrospray) m/z 475 (M + H+). D (1S,2S)-N-(5-(7-(ethyl(methyl)amino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)thiazolo[5,4-b]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 219 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.32 (s, 1H), 13.04 (s, 1H), 9.13 (s, 1H), 8.31 (s, 1H), 7.79 (s, 1H), 7.52 (d, J = 9.3 Hz, 1H), 5.23-4.94 (m, 1H), 2.35-2.17 (m, 4H), 1.86-1.68 (m, 1H), 1.41-1.29 (m, 1H); LCMS(electrospray) m/z 418.0 (M + H+). D (1S,2S)-2-fluoro-N-(6-(6-fluoro-5- (methylthio)-1H-indazol-4-yl)thiazolo[4,5- c]pyridin-2-yl)cyclopropane-1- carboxamide 220 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.60 (s, 1H), 13.10 (s, 1H), 9.12 (s, 1H), 8.53 (s, 1H), 8.14 (s, 1H), 7.63 (d, J = 11.5 Hz, 1H), 5.19-4.96 (m, 1H), 3.17 (s, 3H), 2.29-2.21 (m, 1H), 1.86-1.68 (m, 1H), 1.39-1.29 (m, 1H); LCMS(electrospray) m/z 434.0 (M + H+). D (1S,2S)-2-fluoro-N-(6-(6-fluoro-5- (methylsulfinyl)-1H-indazol-4- yl)thiazolo[4,5-c]pyridin-2- yl)cyclopropane-1-carboxamide 221 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.77 (s, 1H), 9.70 (s, 1H), 9.00 (s, 1H), 8.66 (d, J = 9.2 Hz, 1H), 8.59 (s, 1H), 8.55 (d, J = 9.2 Hz, 1H), 8.33 (d, J = 8.0 Hz, 1H), 8.14 (d, J = 8.8 Hz, 1H), 5.91~5.71 (m, 1H), 3.11 (s, 3H), 3.05~3.00 (m, 1H), 2.54~ 2.48 (m, 1H), 2.07~2.03 (m, 1H); LCMS (electrospray) m/z 350.0 (M + H)+. E (1S,2S)-2-fluoro-N-(6-(5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 222 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.23 (s, 1H), 11.01 (s, 1H), 8.93 (s, 1H), 8.17 (s, 1H), 7.59~7.51 (m, 3H), 7.42 (t, J = 7.8 Hz, 1H), 7.26 (d, J = 6.4 Hz, 1H), 5.00~4.79 (m, 1H), 2.13~2.10 (m, 1H), 1.67~1.60 (m, 1H), 1.17~1.09 (m, 1H); LCMS (electrospray) m/z 335.9 (M + H)+. E (1S,2S)-N-(6-(1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 223 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.92 (s, 1H), 8.13 (s, 1H), 7.99-7.91 (m, 3H), 7.68 (dd, J = 1.0, 8.9 Hz, 1H), 7.58 (d, J = 8.9 Hz, 1H), 1.95- 1.87 (m, 1H), 1.12-1.07 (m, 2H), 1.05-0.98 (m, 2H); LCMS (electrospray) m/z 352.0 (M + H)+. F N-(6-(5-chloro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 224 0embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.98 (s, 1H), 8.17-8.09 (m, 3H), 7.94 (d, J = 9.2 Hz, 1H), 7.71 (d, J = 9.2 Hz, 1H), 7.54-7.48 (m, 1H), 3.90 (s, 3H), 1.94-1.85 (m, 1H), 1.12-1.06 (m, 2H), 1.05-0.99 (m, 2H); LCMS (electrospray) m/z 348.0 (M + H)+. F N-(6-(5-methoxy-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 225 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.76 (s, 1H), 7.88-7.83 (m, 2H), 7.75 (dd, J = 1.5, 9.2 Hz, 1H), 7.66 (dd, J = 0.8, 8.9 Hz, 1H), 7.36 (d, J = 8.9 Hz, 1H), 1.96-1.88 (m, 1H), 1.09-1.04 (m, 2H), 1.02-0.95 (m, 2H); LCMS (electrospray) m/z 333.2 F N-(6-(5-amino-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 3 TFA salt 226 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.43 (br s, 1H), 8.80 (s, 1H), 8.16 (s, 1H), 7.93 (s, 1H), 7.84-7.76 (m, 2H), 7.69 (d, J = 9.4 Hz, 1H), 7.45 (br d, J = 8.9 Hz, 1H), 1.97 (quin, J = 6.2 Hz, 1H), 0.86 (d, J = 6.0 Hz, 4H); LCMS (electrospray) m/z 386.1 (M + H)+. F N-(6-(5-(trifluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 227 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.40 (br s, 1H), 8.83 (s, 1H), 8.14 (s, 1H), 7.75 (d, J = 9.0 Hz, 1H), 7.68 (s, 1H), 7.61 (d, J = 9.0 Hz, 1H), 7.37 (d, J = 10.9 Hz, 1H), 6.90-5.46 (m, 6H), 1.94 (quin, J = 6.2 Hz, 1H), 0.95-0.82 (m, 4H); LCMS (electrospray) m/z 351.2 (M + H)+. F N-(6-(5-amino-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 3TFA salt 228 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.56- 8.53 (m, 1H), 8.11 (s, 1H), 7.82 (s, 1H), 7.68 (d, J = 8.9 Hz, 1H), 7.58-7.50 (m, 2H), 7.38 (dd, J = 1.7, 9.2 Hz, 1H), 1.97-1.88 (m, 1H), 1.02-0.97 (m, 2H), 0.93-0.88 (m, 2H); LCMS (electrospray) m/z 397.9 (M + H)+. F N-(6-(5-bromo-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide 229 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.82 (br s, 1H), 7.89 (br d, J = 8.8 Hz, 1H), 7.82-7.73 (m, 3H), 7.45 (d, J = 8.9 Hz, 1H), 2.98 (s, 3H), 1.98-1.86 (m, 1H), 1.12-0.95 (m, 4H); LCMS (electrospray) m/z 347.0 (M + H)+. F N-(6-(5-(methylamino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 3 TFA salt 230 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.60- 8.57 (m, 1H), 8.09 (s, 1H), 7.87 (s, 1H), 7.58-7.49 (m, 3H), 7.48-7.44 (m, 1H), 2.62 (s, 6H), 1.97- 1.89 (m, 1H), 1.03-0.97 (m, 2H), 0.94-0.88 (m, 2H); LCMS (electrospray) m/z 361.2 (M + H)+. F N-(6-(5-(dimethylamino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide 231 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.05 (s, 1H), 8.78 (s, 1H), 8.14 (s, 1H), 7.92 (s, 1H), 7.64 (d, J = 8.7 Hz, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.32 (dd, J = 1.7, 9.2 Hz, 1H), 2.05-1.86 (m, 1H), 0.85-0.79 (m, 4H); LCMS (electrospray) m/z 414.1 (M + H)+. G N-(6-(5-bromo-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 TFA salt 232 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 9.17 (s, 1H), 8.22 (s, 1H), 8.21-8.18 (m, 1H), 8.06 (d, J = 9.3 Hz, 1H), 7.84 (s, 2H), 1.94-1.87 (m, 1H), 1.14-1.09 (m, 2H), 1.07-1.01 (m, 2H); LCMS (electrospray) m/z 343.0 (M + H)+. F N-(6-(5-cyano-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 233 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.91 (s, 1H), 8.10 (s, 1H), 8.07-8.03 (m, 1H), 8.00-7.96 (m, 1H), 7.91 (s, 1H), 7.72-7.65 (m, 2H), 4.61 (s, 2H), 3.61 (s, 1H), 1.93-1.86 (m, 1H), 1.13-1.08 (m, 2H), 1.07-1.01 (m, 2H); LCMS (electrospray) m/z 348.2 (M + H)+. F N-(6-(5-(hydroxymethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 234 0embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.82 (s, 1H), 8.10 (s, 1H), 8.01-7.95 (m, 1H), 7.95-7.89 (m, 1H), 7.78 (s, 1H), 7.64 (d, J = 8.7 Hz, 1H), 7.50 (d, J = 8.7 Hz, 1H), 2.69 (q, J = 7.5 Hz, 2H), 1.93- 1.85 (m, 1H), 1.19 (t, J = 7.5 Hz, 3H), 1.13-1.07 (m, 2H), 1.07-0.98 (m, 2H); LCMS (electrospray) m/z 346.2 (M + H)+. F N-(6-(5-ethyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 235 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.82 (br s, 1H), 8.90 (s, 1H), 8.19 (s, 1H), 7.91 (d, J = 0.6 Hz, 1H), 7.83 (d, J = 9.2 Hz, 1H), 7.63 (br d, J = 9.2 Hz, 1H), 7.50 (d, J = 11.4 Hz, 1H), 6.54 (dd, J = 11.9, 17.9 Hz, 1H), 5.63 (br d, J = 17.9 Hz, 1H), 5.42 (br d, J = 11.6 Hz, 1H), 2.06-1.94 (m, 1H), 0.95-0.85 (m, 4H); LCMS (electrospray) m/z 362.1 (M + H)+. F N-(6-(6-fluoro-5-vinyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 236 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.46 (br s, 1H), 8.82 (s, 1H), 8.20 (s, 1H), 7.94 (s, 1H), 7.85-7.76 (m, 2H), 7.71 (br d, J = 9.2 Hz, 1H), 7.47 (br d, J = 8.6 Hz, 1H), 5.11-4.85 (m, 1H), 2.20 (td, J = 6.9, 13.9 Hz, 1H), 1.77-1.63 (m, 1H), 1.31-1.16 (m, 1H), 1.31-1.16 (m, 1H); LCMS (electrospray) m/z 403.8 (M + H)+. F (1S,2S)-2-fluoro-N-(6-(5- (trifluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 HCl salt 237 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 11.05 (s, 1H), 8.77 (s, 1H), 8.16 (s, 1H), 7.91 (s, 1H), 7.62 (d, J = 9.7 Hz, 1H), 7.58-7.48 (m, 2H), 7.34 (dd, J = 1.7, 9.2 Hz, 1H), 5.04-4.80 (m, 1H), 2.20-2.10 (m, 1H), 1.73-1.59(m, 1H), 1.23-1.10 (m, 1H); LCMS (electrospray) m/z 370.1 (M + H)+. F (1S,2S)-N-(6-(5-chloro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 238 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.49 (br s, 1H), 8.88 (br s, 1H), 8.20 (s, 1H), 7.90 (s, 1H), 7.73 (br d, J = 9.2 Hz, 1H), 7.69-7.64 (m, 1H), 7.63-7.53 (m, 2H), 5.11-4.86 (m, 1H), 2.19 (br s, 1H), 1.77- 1.62 (m, 1H), 1.22 (br d, J = 2.9 Hz, 1H); LCMS (electrospray) m/z 415.8 (M + H)+. F (1S,2S)-N-(6-(5-bromo-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl salt 239 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.69 (br s, 1H), 8.84 (s, 1H), 8.17 (s, 1H), 8.04 (s, 1H), 7.88 (d, J = 8.8 Hz, 1H), 7.77 (br d, J = 9.0 Hz, 1H), 7.71 (d, J = 8.8 Hz, 1H), 7.59 (br d, J = 8.8 Hz, 1H), 2.40 (s, 3H), 2.03-1.95 (m, 1H), 0.95-0.87 (m, 4H); LCMS (electrospray) m/z 359.9 (M + H)+. F N-(6-(5-acetyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 240 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.27 (s, 1H), 8.99 (s, 1H), 8.21 (s, 1H), 7.98 (d, J = 9.2 Hz, 1H), 7.85 (dd, J = 1.5, 9.1 Hz, 1H), 7.69 (dd, J = 1.0, 8.1 Hz, 2H), 6.23-5.16 (m, 6H), 2.13-2.00 (m, 1H), 1.04-0.87 (m, 4H); LCMS (electrospray) m/z 367.0 (M + H+) F N-(6-(5-amino-6-chloro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 3 HCl salt 241 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.09 (br s, 1H), 9.04 (s, 1H), 8.22 (s, 1H), 7.97-7.86 (m, 3H), 7.41 (d, J = 10.5 Hz, 1H), 2.07-2.00 (m, 1H), 1.99-1.91 (m, 1H), 1.99-1.91 (m, 1H), 0.97-0.87 (m, 4H), 0.78-0.68 (m, 2H), 0.26 (br d, J = 4.5 Hz, 2H); LCMS (electrospray) m/z 376.1 (M + H+) F N-(6-(5-cyclopropyl-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 242 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (br s, 1H), 11.17 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 7.92 (s, 1H), 7.79 (d, J = 1.0 Hz, 1H), 7.68 (dd, J = 0.9, 9.0 Hz, 1H), 6.97 (s, 1H), 6.96 (d, J = 2.0 Hz, 1H), 6.96- 6.93 (m, 1H), 2.13-2.00 (m, 1H), 1.04-0.87 (m, 4H); LCMS (electrospray)m/z 370.8 (M + H+) F N-(6-(5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 243 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.91-11.45 (m, 1H), 9.05-8.93 (m, 1H), 8.24 (br s, 1H), 8.00 (s, 1H), 7.87-7.59 (m, 3H), 5.07 (br s, 1H), 4.91 (br s, 1H), 2.22 (br s, 1H), 1.79-1.63 (m, 1H), 1.23 (br s, 1H); LCMS (electrospray) m/z 388.0 (M + H+) F (1S,2S)-N-(6-(5-chloro-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 HCl salt 244 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.99 (br s, 1H), 8.99 (s, 1H), 8.23 (s, 1H), 7.95-7.85 (m, 2H), 7.82 (d, J = 0.9 Hz, 1H), 7.55 (d, J = 8.7 Hz, 1H), 7.08 (d, J = 8.7 Hz, 1H), 2.07-1.89 (m, 2H), 0.98-0.90 (m, 4H), 0.87-0.81 (m, 2H), 0.69-0.63 (m, 2H); LCMS (electrospray) m/z 358.0 (M + H+) F N-(6-(5-cyclopropyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 245 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.27 (br s, 1H), 8.78 (s, 1H), 8.14 (s, 1H), 7.82 (s, 1H), 7.67 (br d, J = 9.0 Hz, 1H), 7.46 (br d, J = 9.0 Hz, 1H), 7.40 (br d, J = 9.8 Hz, 1H), 2.21 (br d, J = 1.2 Hz, 3H), 2.00- 1.88 (m, 1H), 0.86 (br d, J = 5.7 Hz, 4H); LCMS (electrospray) m/z 350.2 (M + H+) F N-(6-(6-fluoro-5-methyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 TFA salt 246 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.30 (s, 1H), 8.73 (s, 1H), 8.15 (s, 1H), 7.71-7.65 (m, 2H), 7.40 (br d, J = 11.8 Hz, 2H), 3.04 (td, J = 7.0, 14.1 Hz, 1H), 1.98-1.92 (m, 1H), 1.28 (dd, J = 6.9, 17.4 Hz, 6H), 0.87 (d, J = 6.1 Hz, 4H); LCMS (electrospray) m/z 378.1 (M + H+) F N-(6-(6-fluoro-5-isopropyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 TFA salt 247 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.22 (s, 1H), 8.99 (s, 1H), 8.24 (s, 1H), 7.98-7.91 (m, 1H), 7.90- 7.84 (m, 2H), 7.71-7.65 (m, 1H), 7.62-7.57 (m, 1H), 2.40 (s, 3H), 2.11-1.99 (m, 1H), 1.05-0.87 (m, 4H); LCMS (electrospray) m/z 364.1 (M + H+) F N-(6-(5-(methylthio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 248 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.18 (s, 1H), 8.95 (s, 1H), 8.24 (s, 1H), 7.95 (d, J = 9.0 Hz, 1H), 7.81-7.74 (m, 2H), 7.46 (d, J = 10.3 Hz, 1H), 2.58 (q, J = 6.8 Hz, 2H), 2.09-2.00 (m, 1H), 1.09 (t, J = 7.3 Hz, 3H), 0.98-0.87 (m, 4H); LCMS (electrospray) m/z 364.1 (M + H+) F N-(6-(5-ethyl-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 249 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53 (br s, 1H), 11.13 (s, 1H), 8.72 (s, 1H), 8.15 (s, 1H), 7.97 (s, 1H), 7.78-7.74 (m, 1H), 7.73-7.69 (m, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.34 (d, J = 9.0 Hz, 1H), 7.11- 6.80 (m, 1H), 2.00-1.91 (m, 1H), 0.87-0.81 (m, 4H); LCMS (electrospray) m/z 368.2 (M + H+) F N-(6-(5-(difluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 TFA salt 250 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 11.06 (s, 1H), 8.70 (s, 1H), 8.15 (s, 1H), 7.80 (s, 1H), 7.56 (d, J = 9.2 Hz, 1H), 7.38 (d, J = 9.8 Hz, 1H), 7.29 (dd, J = 1.7, 9.2 Hz, 1H), 5.09-4.77 (m, 1H), 2.22 (d, J = 2.4 Hz, 3H), 2.18-2.11 (m, 1H), 1.75-1.58 (m, 1H), 1.24-1.06 (m, 1H); LCMS (electrospray) m/z 368.1 (M + H+) F (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 251 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.92 (br s, 1H), 8.99 (s, 1H), 8.21 (s, 1H), 7.96-7.81 (m, 3H), 7.46 (d, J = 9.9 Hz, 1H), 4.43 (s, 2H), 2.07-1.96 (m, 1H), 0.96-0.87 (m, 4H); LCMS (electrospray) m/z 366.1 (M + H+) F N-(6-(6-fluoro-5-(hydroxymethyl)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 252 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 9.03 (s, 1H), 8.18-8.14 (m, 1H), 8.05 (s, 1H), 7.99 (d, J = 9.2 Hz, 1H), 7.49 (d, J = 10.6 Hz, 1H), 3.77 (s, 3H), 1.95-1.82 (m, 1H), 1.15-1.07 (m, 2H), 1.06- 1.00 (m, 2H); LCMS (electrospray) m/z 366.1 (M + H+) F N-(6-(6-fluoro-5-methoxy-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide. 2 HCl salt 253 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64 (s, 1H), 11.16 (s, 1H), 8.76 (s, 1H), 8.19 (s, 1H), 7.98 (s, 1H), 7.66-7.57 (m, 2H), 7.29 (dd, J = 1.8, 9.1 Hz, 1H), 7.13-6.78 (m, 1H), 5.07-4.80 (m, 1H), 2.16 (td, J = 6.9, 13.9 Hz, 1H), 1.74-1.61 (m, 1H), 1.24- 1.13 (m, 1H); LCMS (electrospray) m/z 404.0 (M + H+) F (1S,2S)-N-(6-(5-(difluoromethyl)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA salt 254 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (s, 1H), 11.11 (s, 1H), 8.79 (s, 1H), 8.17 (s, 1H), 7.93 (s, 1H), 7.65 (d, J = 8.8 Hz, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.32 (dd, J = 1.6, 7.6 Hz, 1H), 5.02 (m, 0.5H), 4.85 (m, 0.5H), 2.16 (m, 1H), 1.66 (m, 1H), 1.16 (m, 1H), LCMS (electrospray) m/z 433.00 (M + H)+. F (1S,2S)-N-(6-(5-bromo-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 255 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.59 (br s, 1H), 11.04 (s, 1H), 8.72 (s, 1H), 8.15 (s, 1H), 7.97 (s, 1H), 7.62-7.56 (m, 2H), 7.23 (dd, J = 1.7, 9.1 Hz, 1H), 7.11-6.80 (m, 1H), 2.01-1.92 (m, 1H), 0.85- 0.79 (m, 4H); LCMS (electrospray) m/z 386.1 (M + H+) F N-(6- (5-(difluoromethyl)-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropanecarboxamide 256 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.14 (s, 1H), 11.13 (s, 1H), 8.87-8.83 (m, 1H), 8.19 (s, 1H), 8.15 (br s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.40 (dd, J = 1.8, 9.2 Hz, 1H), 5.04-4.83 (m, 1H), 2.19- 2.13 (m, 1H), 1.72-1.62 (m, 1H), 1.23-1.15 (m, 1H); LCMS (electrospray) m/z 422.1 (M + H)+. F (1S,2S)-N-(6-(5,7-dichloro-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA salt 257 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (s, 1H), 11.19 (br s, 1H), 8.72 (s, 1H), 8.16 (s, 1H), 7.80 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.37 (br d, J = 9.2 Hz, 1H), 5.10-4.79 (m, 1H), 2.48 (d, J = 1.7 Hz, 3H), 2.21 (d, J = 2.8 Hz, 3H), 2.18-2.10 (m, 1H), 1.75- 1.61 (m, 1H), 1.27-1.10 (m, 1H); LCMS (electrospray) m/z 382.4 (M + H)+. F (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7- dimethyl-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA salt 258 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6)) δ 13.55 (br s, 1H), 11.21 (s, 1H), 8.80 (s, 1H), 8.17 (s, 1H), 7.95 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.43 (d, J = 9.2 Hz, 1H), 5.08-4.77 (m, 1H), 3.01 (s, 3H), 3.00 (s, 3H), 2.16 (td, J = 7.0, 13.8 Hz, 1H), 1.76-1.57 (m, 1H), 1.27-1.11 (m, 1H); LCMS (electrospray) m/z 431.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA salt 259 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.20 (br s, 1H), 8.88 (s, 1H), 8.21 (s, 1H), 8.09 (d, J = 1.1 Hz, 1H), 7.66 (br d, J = 8.3 Hz, 1H), 7.46 (br d, J = 8.8 Hz, 1H), 5.11-4.81 (m, 1H), 2.23-2.11 (m, 1H), 1.96 (s, 3H), 1.93 (s, 3H), 1.75-1.62 (m, 1H), 1.25- 1.13 (m, 1H); LCMS (electrospray) m/z 464.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- (dimethylphosphoryl)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA salt 260 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.17-13.29 (m, 1H), 11.18 (s, 1H), 8.75 (s, 1H), 8.16 (s, 1H), 7.97 (s, 1H), 7.61 (d, J = 9.0 Hz, 1H), 7.36 (dd, J = 1.3, 9.2 Hz, 1H), 5.12-4.77 (m, 1H), 2.26 (d, J = 2.9 Hz, 3H), 2.16 (td, J = 7.0, 14.0 Hz, 1H), 1.76- 1.58 (m, 1H), 1.25-1.10 (m, 1H); LCMS (electrospray) m/z 402.0 (M + H)+. H (1S,2S)-N-(6-(7-chloro-6-fluoro-5-methyl- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA salt 261 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.29 (s, 1H), 8.89 (s, 1H), 8.20 (s, 1H), 8.17 (s, 1H), 7.67 (d, J = 9.0 Hz, 1H), 7.50 (br d, J = 9.4 Hz, 1H), 5.09- 4.82 (m, 1H), 2.18 (td, J = 6.9, 13.9 Hz, 1H), 1.75- 1.62 (m, 1H), 1.26-1.14 (m, 1H); LCMS (electrospray) m/z 466.1 (M + H)+. H (1S,2S)-N-(6-(7-bromo-5-chloro-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 HCl salt 262 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.19 (s, 1H), 8.73 (s, 1H), 8.15 (s, 1H), 7.95 (br s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.35 (d, J = 7.8 Hz, 1H), 5.17-4.75 (m, 1H), 2.25 (d, J = 2.9 Hz, 3H), 2.28-2.12 (m, 1H), 1.72-1.59 (m, 1H), 1.24-1.10 (m, 1H); LCMS (electrospray) m/z 386.3 (M + H)+. H (1S,2S)-N-(6-(6,7-difluoro-5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA salt 263 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.78 (s, 1H), 7.93 (s, 1H), 7.85 (d, J = 9.2 Hz, 1H), 7.71 (d, J = 9.5 Hz, 1H), 5.06-4.94 (m, 1H), 2.31 (d, J = 3.1 Hz, 3H), 2.16-2.09 (m, 1H), 1.93-1.79 (m, 1H), 1.33-1.22 (m, 1H); LCMS (electrospray) m/z 436.0 (M + H)+. H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(trifluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA salt 264 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (br s, 1H), 11.28 (br s, 1H), 8.75 (s, 1H), 8.16 (s, 1H), 7.85 (s, 1H), 7.64 (d, J = 9.0 Hz, 1H), 7.52 (s, 1H), 7.44 (br d, J = 9.0 Hz, 1H), 7.14 (dd, J = 11.4, 17.7 Hz, 1H), 6.12 (br d, J = 17.9 Hz, 1H), 5.51 (d, J = 11.5 Hz, 1H), 5.07-4.86 (m, 1H), 2.34 (s, 3H), 2.16 (td, J = 7.0, 13.8 Hz, 1H), 1.76-1.60 (m, 1H), 1.20 (tdd, J = 6.4, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 376.1 (M + H)+. H (1S,2S)-2-fluoro-N-(6-(5-methyl-7-vinyl- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2TFA salt 265 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.09 (br s, 1H), 11.12 (s, 1H), 8.72 (s, 1H), 8.15 (s, 1H), 7.90 (br s, 1H), 7.56 (d, J = 9.2 Hz, 1H), 7.35 (br d, J = 9.2 Hz, 1H), 5.11-4.75 (m, 1H), 3.17 (br d, J = 2.1 Hz, 3H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 417.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylamino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA salt 266 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.79 (br s, 1H), 11.14 (s, 1H), 8.84 (s, 1H), 8.19 (s, 1H), 8.06 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.41 (dd, J = 1.6, 9.3 Hz, 1H), 5.08-4.80 (m, 1H), 2.58 (s, 3H), 2.22- 2.11 (m, 1H), 1.74-1.60 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 434.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylthio)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA salt 267 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52 (br s, 1H), 11.19 (s, 1H), 8.90 (s, 1H), 8.22 (d, J = 3.4 Hz, 2H), 7.65 (d, J = 9.3 Hz, 1H), 7.44 (dd, J = 1.7, 9.3 Hz, 1H), 5.07-4.80 (m, 1H), 3.56 (s, 3H), 2.21-2.14 (m, 1H), 1.72-1.62 (m, 1H), 1.24-1.15 (m, 1H); LCMS (electrospray) m/z 466.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylsulfonyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA salt 268 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.29 (s, 1H), 8.78 (s, 1H), 8.17 (s, 1H), 7.99 (s, 1H), 7.65 (d, J = 9.1 Hz, 1H), 7.42 (dd, J = 1.6, 9.1 Hz, 1H), 5.08-4.84 (m, 1H), 2.26 (d, J = 3.0 Hz, 3H), 2.21- 2.11 (m, 1H), 1.75-1.62 (m, 1H), 1.20 (tdd, J = 6.3, 9.0, 12.4 Hz, 1H); LCMS (electrospray) m/z 446.2 (M + H)+. H (1S,2S)-N-(6-(7-bromo-6-fluoro-5-methyl- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA salt 269 05embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.22 (s, 1H), 8.76 (s, 1H), 8.16 (s, 1H), 7.89 (s, 1H), 7.64 (d, J = 9.0 Hz, 1H), 7.41 (dd, J = 1.6, 9.1 Hz, 1H), 5.06- 5.02 (m, 1H), 4.90-4.84 (m, 1H), 2.52 (s, 3H), 2.23 (d, J = 2.9 Hz, 3H), 2.20-2.12 (m, 1H), 1.75- 1.63 (m, 1H), 1.26-1.14 (m, 1H); LCMS (electrospray) m/z 414.1 (M + H)+. H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA salt 270 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.23 (br s, 1H), 11.20 (s, 1H), 8.79 (s, 1H), 8.19 (s, 1H), 8.03 (s, 1H), 7.64 (d, J = 9.2 Hz, 1H), 7.37 (dd, J = 1.7, 9.1 Hz, 1H), 5.06-4.84 (m, 1H), 3.50 (br s, 3H), 2.27 (d, J = 2.8 Hz, 3H), 2.21-2.12 (m, 1H), 1.73-1.62 (m, 1H), 1.23-1.14 (m, 1H); LCMS (electrospray) m/z 446.2 (M + H)+. H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylsulfonyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA salt 271 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (br s, 1H), 11.27 (s, 1H), 8.73 (s, 1H), 8.16 (s, 1H), 7.84 (s, 1H), 7.64 (d, J = 9.3 Hz, 1H), 7.41 (dd, J = 1.4, 9.1 Hz, 1H), 5.13-4.79 (m, 1H), 4.08 (d, J = 1.0 Hz, 3H), 2.22 (d, J = 3.1 Hz, 3H), 2.20-2.10 (m, 1H), 1.77-1.60 (m, 1H), 1.20 (tdd, J = 6.3, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 398.2 (M + H)+. H (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- methoxy-5-methyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA salt 272 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.81 (br s, 1H), 11.15 (s, 1H), 8.80 (s, 1H), 8.17 (s, 1H), 8.00 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 1.6, 9.2 Hz, 1H), 5.12-4.81 (m, 1H), 4.16 (d, J = 1.5 Hz, 3H), 2.22-2.11 (m, 1H), 1.75-1.60 (m, 1H), 1.18 (tdd, J = 6.3, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 418.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- methoxy-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA salt 273 09embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.90 (br s, 1H), 8.63 (s, 1H), 8.13 (s, 1H), 7.73 (s, 1H), 7.61 (d, J = 9.0 Hz, 1H), 7.36 (d, J = 9.2 Hz, 1H), 5.03-4.80 (m, 1H), 3.00 (s, 6H), 2.19 (d, J = 2.9 Hz, 3H), 2.18- 2.14 (m, 1H), 1.78-1.65 (m, 1H), 1.24-1.14 (m, 1H); LCMS (electrospray) m/z 411.2 (M + H)+. H (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-methyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA salt 274 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.29 (s, 1H), 10.19 (s, 1H), 8.75 (s, 1H), 8.16 (s, 1H), 7.82 (s, 1H), 7.66 (s, 1H), 7.64 (s, 1H), 7.45 (br d, J = 9.9 Hz, 1H), 6.61-6.51 (m, 1H), 6.35 (dd, J = 1.8, 16.9 Hz, 1H), 5.89-5.84 (m, 1H), 5.08-5.03 (m, 1H), 4.89 (dt, J = 3.8, 6.3 Hz, 1H), 2.32 (s, 3H), 2.21- 2.12 (m, 1H), 1.76-1.60 (m, 1H), 1.27-1.14 (m, 1H); LCMS (electrospray) m/z 419.3 (M + H)+. H (1S,2S)-N-(6-(7-acrylamido-5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA salt 275 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.80 (br s, 1H), 11.18 (s, 1H), 8.82 (s, 1H), 8.17 (s, 1H), 8.00 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.42 (dd, J = 1.5, 9.3 Hz, 1H), 5.11-4.81 (m, 1H), 4.40 (q, J = 7.1 Hz, 2H), 2.21-2.10 (m, 1H), 1.74-1.61 (m, 1H), 1.41 (t, J = 7.0 Hz, 3H), 1.25-1.09 (m, 1H); LCMS (electrospray) m/z 432.3 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-ethoxy-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA salt 276 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.23-11.08 (m, 1H), 10.40-10.29 (m, 1H), 8.80 (s, 1H), 8.17 (s, 1H), 8.01 (br d, J = 7.9 Hz, 2H), 7.59 (br d, J = 9.0 Hz, 1H), 7.46-7.36 (m, 1H), 6.66-6.49 (m, 1H), 6.41-6.36 (m, 1H), 5.95-5.85 (m, 1H), 5.12-4.78 (m, 1H), 2.22-2.08 (m, 1H), 1.77-1.58 (m, 1H), 1.27-1.10 (m, 1H); LCMS (electrospray) m/z 439.2 (M + H)+. H (1S,2S)-N-(6-(7-acrylamido-5-chloro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA salt 277 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 9.88 (br d, J = 6.7 Hz, 1H), 8.77 (dd, J = 1.0, 1.6 Hz, 1H), 8.19 (s, 1H), 8.03 (br s, 1H), 7.60 (d, J = 9.2 Hz, 1H), 7.36 (dd, J = 1.8, 9.2 Hz, 1H), 5.05- 5.00 (m, 1H), 4.86 (dt, J = 3.9, 6.2 Hz, 1H), 3.58 (br d, J = 11.0 Hz, 4H), 3.53-3.44 (m, 2H), 3.39- 3.26 (m, 2H), 2.93 (br d, J = 2.7 Hz, 3H), 2.20- 2.12 (m, 1H), 1.73-1.61 (m, 1H), 1.24-1.13 (m, 1H); LCMS (electrospray) m/z 486.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(4- methylpiperazin-1-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 TFA 278 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.09 (br s, 1H), 10.92 (s, 1H), 8.64 (s, 1H), 8.13 (s, 1H), 7.75 (s, 1H), 7.52 (d, J = 9.2 Hz, 1H), 7.48 (d, J = 8.3 Hz, 1H), 7.32 (d, J = 8.6 Hz, 1H), 7.26 (dd, J = 1.7, 9.2 Hz, 1H), 4.46 (t, J = 5.2 Hz, 1H), 3.69-3.60 (m, 1H), 3.55-3.48 (m, 1H), 2.32 (s, 3H), 2.08-1.99 (m, 1H), 1.49-1.39 (m, 1H), 1.02-0.96 (m, 1H), 0.95-0.90 (m, 1H); LCMS (electrospray) m/z 362.3 (M + H)+. H 2-(hydroxymethyl)-N-(6-(5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 279 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (br s, 1H), 11.21 (s, 1H), 8.81 (s, 1H), 8.18 (s, 1H), 7.98 (s, 1H), 7.62 (d, J = 9.3 Hz, 1H), 7.43 (dd, J = 1.6, 9.2 Hz, 1H), 5.07-4.84 (m, 1H), 3.84-3.82 (m, 4H), 3.29 (br s, 4H), 2.21-2.12 (m, 1H), 1.74-1.61(m, 1H), 1.19 (tdd, J = 6.4, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 473.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- morpholino-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 280 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.23 (1 H, s) 8.78 (1 H, s) 8.16 (1 H, s) 7.93 (1 H, br s) 7.61 (1 H, d, J = 9.20 Hz) 7.44 (1 H, br d, J = 9.40 Hz) 5.16- 4.71 (1 H, m) 2.17 (1 H, dt, J = 14.07, 6.97 Hz) 1.76-1.61 (1 H, m) 1.27-1.17 (4 H, m); LCMS (electrospray) m/z 431.0 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(ethylamino)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 281 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (1 H, br s) 11.38-11.10 (1 H, m) 8.99-8.77 (1 H, m) 8.17 (1 H, s) 7.96 (1 H, s) 7.77-7.57 (1 H, m) 7.53-7.35 (1 H, m) 5.14-4.79 (1 H, m) 3.39-3.37 (1 H, m) 3.30 (4 H, q, J = 7.01 Hz) 2.17 (1 H, dt, J = 13.88, 7.00 Hz) 1.79-1.59 (1 H, m) 1.27-1.12 (1 H, m) 1.06-0.95 (6 H, m); LCMS (electrospray) m/z 459.0 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(diethylamino)- 6-fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 282 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (br s, 1H), 11.16 (s, 1H), 8.74 (s, 1H), 8.16 (s, 1H), 7.93 (br s, 1H), 7.58 (d, J = 9.0 Hz, 1H), 7.37 (dd, J = 1.5, 9.2 Hz, 1H), 5.07-4.82 (m, 1H), 3.72 (br s, 4H), 2.21- 2.12 (m, 1H), 1.98-1.93 (m, 4H), 1.73-1.62 (m, 1H), 1.24-1.13 (m, 1H); LCMS (electrospray) m/z 457.3 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (pyrrolidin-1-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 283 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.08 (br s, 1H), 11.08 (s, 1H), 8.70 (s, 1H), 8.14 (s, 1H), 7.89 (br s, 1H), 7.54 (d, J = 9.3 Hz, 1H), 7.30 (dd, J = 1.6, 9.3 Hz, 1H), 5.06-4.79 (m, 1H), 4.39 (br t, J = 5.7 Hz, 4H), 2.39-2.32 (m, 2H), 2.15 (td, J = 7.0, 13.7 Hz, 1H), 1.72-1.61 (m, 1H), 1.22-1.13 (m, 1H); LCMS (electrospray) m/z 443.4 (M + H)+. H (1S,2S)-N-(6-(7-(azetidin-1-yl)-5-chloro- 6-fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 284 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.22-11.10 (m, 1H), 8.76 (br s, 1H), 8.17 (s, 1H), 7.62-7.56 (m, 2H), 7.43-7.32 (m, 1H), 6.87 (s, 1H), 5.07- 4.83 (m, 1H), 2.21-2.10 (m, 1H), 1.75-1.60 (m, 1H), 1.25-1.13 (m, 1H); LCMS(electrospray) m/z 385.4 (M + H+). H (1S,2S)-N-(6-(6-amino-5-chloro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 285 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (br s, 1H), 11.28 (s, 1H), 8.69 (s, 1H), 8.15 (s, 1H), 7.73 (s, 1H), 7.63 (d, J = 9.1 Hz, 1H), 7.43 (br d, J = 9.1 Hz, 1H), 6.83 (s, 1H), 5.08-4.86 (m, 1H), 3.99 (s, 3H), 2.32 (s, 3H), 2.21-2.12 (m, 1H), 1.75-1.63 (m, 1H), 1.27-1.12 (m, 1H); LCMS(electrospray) m/z 380.5 (M + H+). H (1S,2S)-2-fluoro-N-(6-(7-methoxy-5- methyl-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 286 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53-13.11 (m, 1H), 11.23-11.11 (m, 1H), 9.82 (s, 1H), 8.80 (br s, 1H), 8.17 (d, J = 11.5 Hz, 2H), 7.89 (s, 1H), 7.65-7.57 (m, 1H), 7.43-7.32 (m, 1H), 6.72 (dd, J = 10.3, 17.1 Hz, 1H), 6.32 (dd, J = 1.9, 17.0 Hz, 1H), 5.85-5.80 (m, 1H), 5.07-4.83 (m, 1H), 2.20- 2.12 (m, 1H), 1.73-1.61 (m, 1H), 1.23-1.14 (m, 1H); LCMS (electrospray) m/z 439.3 (M + H+). H (1S,2S)-N-(6-(6-acrylamido-5-chloro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 287 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30 (br s, 1H), 11.29 (s, 1H), 8.69 (s, 1H), 8.15 (s, 1H), 7.73 (s, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.43 (br d, J = 8.4 Hz, 1H), 6.82 (s, 1H), 5.07-4.86 (m, 1H), 4.28 (q, J = 6.9 Hz, 3H), 2.31 (s, 3H), 2.20-2.12 (m, 1H), 1.75-1.63 (m, 1H), 1.46 (t, J = 7.0 Hz, 3H), 1.21 (tdd, J = 6.3, 9.0, 12.5 Hz, 1H); LCMS(electrospray) m/z 394.1 (M + H+). H (1S,2S)-N-(6-(7-etho xy-5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 288 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (br s, 1H), 11.21 (s, 1H), 8.71 (s, 1H), 8.15 (s, 1H), 7.83 (s, 1H), 7.61 (d, J = 9.2 Hz, 1H), 7.38 (dd, J = 1.3, 9.2 Hz, 1H), 5.12-4.79 (m, 1H), 4.31 (q, J = 7.0 Hz, 2H), 2.22 (d, J = 3.1 Hz, 3H), 2.20-2.11 (m, 1H), 1.74-1.60 (m, 1H), 1.39 (t, J = 7.0 Hz, 3H), 1.19 (tdd, J = 6.4, 9.1, 12.4 Hz, 1H); LCMS(electrospray) m/z 412.1 (M + H+). H (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5- methyl-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 289 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.72 (s, 1H), 7.88-7.81 (m, 2H), 7.79 (s, 1H), 7.73 (br d, J = 8.8 Hz, 1H), 6.64-6.55 (m, 1H), 6.49-6.41 (m, 1H), 5.87 (br d, J = 11.6 Hz, 1H), 5.07-4.97 (m, 2H), 2.26 (s, 3H), 2.19-2.09 (m, 1H), 1.94- 1.81 (m, 1H), 1.35-1.23 (m, 1H); LCMS(electrospray) m/z 419.2 (M + H+). H (1S,2S)-N-(6-(6-acrylamido-5-methyl-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 290 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.80 (br s, 1H), 11.19 (s, 1H), 8.87 (s, 1H), 8.18 (s, 1H), 8.07 (s, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.46 (dd, J = 1.7, 9.2 Hz, 1H), 5.06-4.83 (m, 1H), 3.51-3.50 (m, 2H), 3.08 (t, J = 6.7 Hz, 2H), 2.22-2.12 (m, 1H), 1.74- 1.61 (m, 1H), 1.19 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 464 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((2- hydroxyethyl)thio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 291 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.54-11.33 (m, 1H), 8.73 (br d, J = 3.3 Hz, 1H), 8.18 (d, J = 1.6 Hz, 1H), 7.78-7.61 (m, 2H), 7.47 (br t, J = 9.4 Hz, 1H), 5.12-4.85 (m, 1H), 2.98 (s, 3H), 2.97 (s, 3H), 2.56 (br d, J = 7.3 Hz, 2H), 2.17 (td, J = 6.9, 13.7 Hz, 1H), 1.78-1.59 (m, 1H), 1.29-1.21 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 425.2 (M + H+). H (1S,2S)-N-(6-(7-(dimethylamino)-5-ethyl- 6-fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 292 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (br s, 1H), 11.22 (s, 1H), 8.77 (s, 1H), 8.16 (s, 1H), 7.90 (s, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.41 (dd, J = 1.5, 9.2 Hz, 1H), 5.06-4.85 (m, 1H), 3.50 (t, J = 6.9 Hz, 2H), 3.02 (t, J = 6.9 Hz, 2H), 2.23 (d, J = 2.9 Hz, 3H), 2.19-2.13 (m, 1H), 1.74-1.60 (m, 1H), 1.19 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 444 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-7-((2- hydroxyethyl)thio)-5-methyl-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 293 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.89-13.08 (m, 1H), 11.22 (br s, 1H), 8.72 (s, 1H), 8.17 (s, 1H), 7.81 (s, 1H), 7.63 (br d, J = 9.1 Hz, 1H), 7.35 (br d, J = 9.1 Hz, 1H), 5.07-4.83 (m, 1H), 2.62-2.58 (m, 2H), 2.53 (s, 3H), 2.16 (td, J = 6.9, 13.9 Hz, 1H), 1.74-1.60 (m, 1H), 1.24-1.15 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 428.3 (M + H+). H (1S,2S)-N-(6-(5-ethyl-6-fluoro-7- (methylthio)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 294 0embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 11.24 (s, 1H), 8.73 (s, 1H), 8.18 (s, 1H), 7.75 (s, 1H), 7.64 (d, J = 9.0 Hz, 1H), 7.42 (d, J = 10.4 Hz, 1H), 7.36 (br d, J = 9.0 Hz, 1H), 5.12-4.76 (m, 1H), 2.61 (br d, J = 7.3 Hz, 2H), 2.23-2.12 (m, 1H), 1.77-1.62 (m, 1H), 1.22-1.16 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 382.3 (M + H+). H (1S,2S)-N-(6-(5-ethyl-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 295 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.51 (d, J = 7.2 Hz, 1H), 7.85 (s, 1H), 7.66 (s, 1H), 7.00- 6.91 (m, 2H), 5.03-4.96 (m, 1H), 2.16-2.07 (m, 1H), 1.89-1.78 (m, 1H), 1.30-1.17 (m, 1H); LCMS(electrospray) m/z 404.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- hydroxy-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 296 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 11.23 (s, 1H), 8.77 (s, 1H), 8.17 (s, 1H), 7.90 (s, 1H), 7.61 (d, J = 9.0 Hz, 1H), 7.54 (d, J = 9.3 Hz, 1H), 7.45 (br d, J = 9.3 Hz, 1H), 5.12-4.81 (m, 1H), 2.25 (s, 3H), 2.21-2.11 (m, 1H), 1.75-1.61 (m, 1H), 1.25-1.21 (m, 1H); LCMS(electrospray) m/z 400.2 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5- (methylthio)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 297 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.17 (s, 1H), 8.75 (d, J = 0.7 Hz, 1H), 8.17 (s, 1H), 7.97 (s, 1H), 7.59 (br d, J = 9.2 Hz, 1H), 7.44-7.39 (m, 1H), 5.16-4.80 (m, 1H), 2.56-2.54 (m, 3H), 2.38-2.30 (m, 1H), 2.27 (s, 3H), 2.21-2.11 (m, 1H), 1.77- 1.62 (m, 1H), 1.25-1.12 (m, 1H); LCMS(electrospray) m/z 446.0 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5,7- bis(methylthio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 298 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 13.00 (s, 1 H), 8.34-8.22 (m, 2 H), 7.92 (d, J = 9.17 Hz, 1 H), 7.71-7.61 (m, 2 H), 5.01-4.74 (m, 1 H), 2.67 (br d, J = 7.34 Hz, 2 H), 2.20-2.15 (m, 1 H), 2.06-1.96 (m, 2 H), 1.33-1.23 (m, 1 H), 1.17 (t, J = 7.46 Hz, 3 H); LCMS(electrospray) m/z 400.0 (M + H+). H (1S,2S)-N-(6-(5-ethyl-6,7-difluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 299 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.74 (s, 1H), 8.18 (s, 1H), 7.97 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.36 (br d, J = 8.9 Hz, 1H), 5.09-4.78 (m, 1H), 3.13 (s, 3H), 2.23 (d, J = 2.8 Hz, 3H), 2.20- 2.11 (m, 1H), 1.73-1.62 (m, 1H), 1.24-1.12 (m, 1H); LCMS(electrospray) m/z 429.11 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylsulfinyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 300 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (br s, 1H), 11.22 (s, 1H), 8.71 (s, 1H), 8.16 (s, 1H), 7.86 (s, 1H), 7.60 (d, J = 9.2 Hz, 1H), 7.43 (br d, J = 9.0 Hz, 1H), 5.08-4.85 (m, 1H), 2.99 (d, J = 2.3 Hz, 6H), 2.27 (s, 3H), 2.21-2.12 (m, 1H), 1.76-1.61 (m, 1H), 1.26-1.16 (m, 1H); LCMS(electrospray) m/z 443 (M + H+). H (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 301 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.20 (s, 1H), 10.15 (s, 1H), 8.87 (s, 1H), 8.19 (s, 1H), 7.98 (s, 1H), 7.64 (d, J = 9.3 Hz, 1H), 7.46 (dd, J = 1.5, 9.2 Hz, 1H), 5.08-4.82 (m, 1H), 2.18 (s, 3H), 2.17- 2.11 (m, 1H), 1.74-1.62 (m, 1H), 1.26-1.15 (m, 1H); LCMS(electrospray) m/z 445.2 (M + H+). H (1S,2S)-N-(6-(7-acetamido-5-chloro-6- fluoro-1H-indazol-4-yfiimidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 302 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38-13.09 (m, 1H), 11.19 (s, 1H), 8.80 (s, 1H), 8.19 (s, 1H), 8.03 (s, 1H), 7.64 (d, J = 9.1 Hz, 1H), 7.38 (dd, J = 1.6, 9.2 Hz, 1H), 5.09-4.78 (m, 1H), 3.50 (s, 3H), 2.27 (d, J = 2.8 Hz, 3H), 2.21-2.12 (m, 1H), 1.74- 1.61 (m, 1H), 1.19 (tdd, J = 6.3, 9.0, 12.4 Hz, 1H); LCMS(electrospray) m/z 446.0 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(methylsulfonyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 303 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.15 (s, 1H), 8.87 (d, J = 0.6 Hz, 1H), 8.20 (s, 1H), 8.15 (s, 1H), 7.63 (d, J = 9.3 Hz, 1H), 7.42 (dd, J = 1.7, 9.3 Hz, 1H), 5.07-4.82 (m, 1H), 3.19 (s, 3H), 2.21-2.11 (m, 1H), 1.74-1.61 (m, 1H), 1.24-1.12 (m, 1H); LCMS(electrospray) m/z 450 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methylsulfinyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 304 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.28 (br s, 1H), 8.77 (s, 1H), 8.17 (s, 1H), 8.05 (br d, J = 2.0 Hz, 1H), 7.63 (br d, J = 9.1 Hz, 1H), 7.45 (br d, J = 9.1 Hz, 1H), 5.06-5.02 (m, 1H), 4.89-4.87 (m, 1H), 2.30 (s, 3H), 2.21-2.12 (m, 1H), 1.75-1.61 (m, 1H), 1.24-1.13 (m, 1H); LCMS(electrospray) m/z 418 (M + H+). H (1S,2S)-N-(6-(6,7-difluoro-5-(methylthio)- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 1 TFA 305 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.80 (s, 1H), 7.89-7.86 (m, 2H), 7.77 (d, J = 8.9 Hz, 1H), 5.05-4.96 (m, 1H), 4.06 (s, 3H), 2.30 (d, J = 3.1 Hz, 3H), 2.13 (ddd, J = 2.3, 4.5, 6.6 Hz, 1H), 1.91- 1.81 (m, 1H), 1.31-1.25 (m, 1H); LCMS(electrospray) m/z 426.2 (M + H+). H methyl 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 5-methyl-1H-indazole-7-carboxylate 306 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.27 (s, 1H), 8.84 (s, 1H), 8.17 (s, 1H), 7.95 (s, 1H), 7.65 (d, J = 9.2 Hz, 1H), 7.49 (dd, J = 1.6, 9.2 Hz, 1H), 5.04 (dt, J = 3.8, 6.2 Hz, 1H), 4.89-4.85 (m, 1H), 3.27 (q, J = 6.9 Hz, 2H), 2.98 (d, J = 2.6 Hz, 3H), 2.20- 2.12 (m, 1H), 1.73-1.63 (m, 1H), 1.20 (tdd, J = 6.3, 9.0, 12.4 Hz, 1H), 1.08 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 445.2 (M + H+). H (1S,2S)-N-(6-(5-chloro-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 1 TFA 307 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 8.68 (s, 1H), 8.13 (s, 1H), 7.86 (br d, J = 3.4 Hz, 1H), 7.55 (d, J = 9.2 Hz, 1H), 7.24 (d, J = 9.2 Hz, 1H), 5.06-4.79 (m, 1H), 3.02 (d, J = 2.0 Hz, 6H), 2.21-2.11 (m, 1H), 1.73-1.61 (m, 1H), 1.21 1.11 (m, 1H); LCMS(electrospray) m/z 465.1 (M + H+). H (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-5-(trifluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 308 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.14-12.81 (m, 1H), 11.30-11.11 (m, 1H), 9.94 (s, 1H), 8.75 (s, 1H), 8.16 (s, 1H), 7.80 (s, 1H), 7.66-7.59 (m, 1H), 7.43-7.32 (m, 1H), 5.07-4.81 (m, 1H), 2.22 (d, J = 2.9 Hz, 3H), 2.16 (s, 4H), 1.74-1.62 (m, 1H), 1.27-1.12 (m, 1H); LCMS(electrospray) m/z 424.15 (M + H+). H (1S,2S)-N-(6-(7-acetamido-6-fluoro-5- methyl-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 309 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.29 (s, 1H), 11.07 (s, 1H), 8.74 (s, 1H), 8.41 (s, 1H), 7.93 (s, 1H), 7.54 (d, J = 9.2 Hz, 1H), 7.29 (d, J = 9.2 Hz, 1H), 5.01-4.83 (m, 1H), 3.22 (s, 3H), 2.23-2.16 (m, 1H), 1.78-1.61 (m, 1H), 1.23 (br, 9H), 1.28- 1.12 (m, 1H); LCMS (electrospray) m/z 532.1 (M + H)+. H tert-butyl 2-(5-chloro-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazol-7-yl)-1-methylhydrazine-1- carboxylate 310 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.02-13.34 (m, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.0 Hz, 1H), 7.85 (s, 1H), 7.65 (s, 1H), 6.93 (s, 1H), 6.89 (dd, J = 1.8, 7.1 Hz, 1H), 5.11-4.78 (m, 1H), 4.35 (q, J = 7.0 Hz, 2H), 2.28 (s, 3H), 2.19-2.12 (m, 1H), 1.68 (m, J = 3.2, 6.8, 19.9 Hz, 1H), 1.41 (t, J = 7.0 Hz, 3H), 1.26-1.11 (m, 1H); LCMS(electrospray) m/z 444.2 (M + H+). H (1S,2S)-N-(6-(7-ethoxy-6-fluoro-5- (methylthio)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 311 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 10.85 (br s, 1H), 8.70 (s, 1H), 8.15 (s, 1H), 7.89 (s, 1H), 7.60 (d, J = 9.0 Hz, 1H), 7.36 (dd, J = 1.5, 9.1 Hz, 1H), 5.05- 4.79 (m, 2H), 2.27 (br d, J = 2.6 Hz, 3H), 1.80 (s, 3H), 1.77-1.63 (m, 1H), 1.18 (tdd, J = 6.3, 9.2, 12.2 Hz, 1H); LCMS(electrospray) m/z 438.16 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(N-methylacetamido)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 312 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.78 (s, 1H), 7.91-7.83 (m, 3H), 7.80-7.75 (m, 1H), 5.01 (dt, J = 3.9, 6.2 Hz, 1H), 4.13 (br t, J = 6.5 Hz, 2H), 3.17 (br t, J = 6.7 Hz, 2H), 2.63 (s, 3H), 2.29 (d, J = 2.9 Hz, 3H), 2.17-2.09 (m, 1H), 1.92-1.81 (m, 1H), 1.31-1.26 (m, 1H); LCMS(electrospray) m/z501.3 (M + H+). H 2-((6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 5-methyl-1H-indazol-7-yl)thio)ethyl methylcarbamate. 1 TFA 313 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.19(br s, 1H), 11.16 (s, 1H), 8.79 (s, 1H), 8.17 (s, 1H), 7.91 (s, 1H), 7.61 (d, J = 9.0 Hz, 1H), 7.36 (br d, J = 8.9 Hz, 1H), 5.04-4.85(m, 1H), 2.23 (d, J = 3.1 Hz, 3H), 2.19-2.16 (m, 1H), 1.72-1.63 (m, 1H), 1.18 (ddd, J = 2.6, 6.2, 9.2 Hz, 1H); LCMS(electrospray) m/z 412.1 (M + H+). H 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 5-methyl-1H-indazole-7-carboxylic acid. 1 TFA 314 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.13 (s, 1H), 8.88 (s, 1H), 8.19 (s, 1H), 8.08 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.41 (dd, J = 1.8, 9.2 Hz, 1H), 5.06-4.83 (m, 1H), 2.22-2.12 (m, 1H), 1.74-1.57 (m, 1H), 1.29-1.06 (m, 1H); LCMS(electrospray) m/z 432.2 (M + H+). H 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazole-7-carboxylic acid. 1 TFA 315 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69-13.54 (m, 1H), 11.16 (s, 1H), 8.90 (s, 1H), 8.20 (s, 1H), 8.13 (s, 1H), 7.63 (br d, J = 9.2 Hz, 1H), 7.44 (br d, J = 9.4 Hz, 1H), 5.12 (d, J = 6.5 Hz, 1H), 4.01 (s, 3H), 2.23-2.11 (m, 1H), 1.76-1.61 (m, 1H), 1.28-1.08 (m, 1H); LCMS(electrospray) m/z 446.2 (M + H+). H methyl 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazole-7-carboxylate. 1 TFA 316 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.22-13.73 (m, 1H), 11.15 (s, 1H), 8.87-8.86 (m, 1H), 8.19 (s, 1H), 8.13 (s, 1H), 7.62 (d, J = 9.3 Hz, 1H), 7.47- 7.40 (m, 1H), 5.04-4.84 (m, 1H), 3.23 (s, 3H), 2.17 (ddd, J = 2.0, 5.0, 6.9 Hz, 1H), 1.82 (s, 3H), 1.71-1.63 (m, 1H), 1.19-1.13 (m, 1H); LCMS(electrospray) m/z 459.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(N- methylacetamido)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 317 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.93 (s, 1H), 11.06 (s, 1H), 8.70 (s, 1H), 8.14 (s, 1H), 7.79 (s, 1H), 7.52 (d, J = 9.2 Hz, 1H), 7.38 (s, 1H), 7.31 (d, J = 9.2 Hz, 1H), 5.01-4.83 (m, 1H), 5.01 (s, 1H), 2.60 (s, 3H), 2.23-2.16 (m, 1H), 1.78-1.61 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 432.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- methylhydrazineyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 318 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.60-13.32 (m, 1H), 11.06 (s, 1H), 8.63 (s, 1H), 8.15 (s, 1H), 7.74 (s, 1H), 7.54 (d, J = 9.1 Hz, 1H), 7.21 (dd, J = 1.6, 9.1 Hz, 1H), 5.04-4.82 (m, 1H), 4.32 (q, J = 7.0 Hz, 2H), 2.60 (br d, J = 6.6 Hz, 2H), 2.20-2.11 (m, 1H), 1.72-1.61 (m, 1H), 1.39 (t, J = 6.9 Hz, 3H), 1.20-1.13 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 426.0 (M + H+). H (1S,2S)-N-(6-(7-ethoxy-5-ethyl-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 319 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.73 (s, 1H), 11.13 (s, 1H), 8.89 (s, 1H), 8.22 (s, 1H), 8.10 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.40 (dd, J = 1.5, 9.2 Hz, 1H), 5.08-4.81 (m, 1H), 2.77 (d, J = 6.1 Hz, 3H), 2.25-2.12 (m, 1H), 1.76-1.61 (m, 1H), 1.13- 1.19 (m, J = 2.9, 6.1, 12.1 Hz, 1H); LCMS(electrospray) m/z 430.3(M + H+). H (1S,2S)-N-(6-(7-acetyl-5-chloro-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 320 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.10 (s, 1H), 8.89 (s, 1H), 8.19 (s, 1H), 8.06 (s, 1H), 7.60 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 1.7, 9.3 Hz, 1H), 5.10- 4.79 (m, 1H), 3.13 (s, 3H), 2.93 (s, 3H), 2.21-2.12 (m, 1H), 1.75-1.60 (m, 1H), 1.08 (s, 1H); LCMS(electrospray) m/z 459.0 (M + H+). H 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N,N-dimethyl-1H-indazole-7-carboxamide 321 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.19-11.05 (m, 1H), 8.90-8.81 (m, 1H), 8.69-8.61 (m, 1H), 8.49-8.44 (m, 1H) 8.26-8.16 (m, 1H) 8.07-8.00 (m, 1H), 7.68-7.54 (m, 1H), 7.42-7.31 (m, 1H), 5.15-4.75 (m, 1H), 2.91 (d, J = 4.2 Hz, 3H), 2.23- 2.11 (m, 1H), 1.76 (br d, J = 4.8 Hz, 1H), 1.27- 1.10 (m, 1H); LCMS(electrospray) m/z 445.3 (M + H+). H 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N-methyl-1H-indazole-7-carboxamide 322 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43 (s, 1H), 11.10 (s, 1H), 8.77 (s, 1H), 8.18 (s, 1H), 7.92 (s, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.31 (dd, J = 1.6, 9.2 Hz, 1H), 5.08-4.79 (m, 1H), 2.74 (d, J = 6.2 Hz, 3H), 2.28 (d, J = 3.2 Hz, 3H), 2.16 (td, J = 6.9, 13.9 Hz, 1H), 1.75-1.58 (m, 1H), 1.17 (tdd, J = 6.3, 9.1, 12.2 Hz, 1H); LCMS(electrospray) m/z 409.14 (M + H+). H (1S,2S)-N-(6-(7-acetyl-6-fluoro-5-methyl- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 323 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.21-11.16 (m, 1H), 8.83 (s, 1H), 8.18 (s, 1H), 8.15 (br s, 1H), 7.71-7.59 (m, 1H), 7.41 (dd, J = 1.6, 9.2 Hz, 1H), 5.06-4.83 (m, 1H), 2.22-2.11 (m, 1H), 1.74-1.59 (m, 1H), 1.19 (tdd, J = 6.4, 9.1, 12.4 Hz, 1H); LCMS(electrospray) m/z 406.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6,7-difluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 324 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (br s, 1H), 11.06 (s, 1H), 8.66 (s, 1H), 8.13 (s, 1H), 7.84 (br s, 1H), 7.51 (d, J = 9.1 Hz, 1H), 7.30 (br d, J = 8.5 Hz, 1H), 5.06-4.81 (m, 1H), 3.25-3.20 (m, 2H), 2.95 (br s, 3H), 2.25 (s, 3H), 2.16-2.15 (m, 1H), 1.70-1.63 (m, 1H), 1.19-1.13 (m, 1H), 1.07 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 457 (M + H+). H (1S,2S)-N-(6-(7-(ethyl(methyl)amino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 325 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (s, 1H), 11.12 (s, 1H), 8.86 (s, 1H), 8.20 (s, 1H), 8.05 (d, J = 16.9 Hz, 3H), 7.61 (d, J = 9.2 Hz, 1H), 7.38 (dd, J = 1.6, 9.2 Hz, 1H), 5.11-4.79 (m, 1H), 2.24- 2.08 (m, 1H), 1.78-1.57 (m, 1H), 1.21-1.14 (m, 1H); LCMS(electrospray) m/z 431.1 (M + H+). H 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazole-7-carboxamide 326 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (br s, 1H), 11.06 (s, 1H), 8.63 (s, 1H), 8.14 (s, 1H), 7.68 (s, 1H), 7.53 (d, J = 9.2 Hz, 1H), 7.22 (d, J = 9.3 Hz, 1H), 5.06-4.78 (m, 1H), 3.27-3.11 (m, 2H), 2.94 (s, 4H), 2.57 (br d, J = 6.8 Hz, 2H), 2.21-2.09 (m, 1H), 1.76-1.58 (m, 1H), 1.25-1.14 (m, 1H), 1.11- 1.04 (m, 6H); LCMS(electrospray) m/z 439.2 (M + H+). H (1S,2S)-N-(6-(5-ethyl-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 327 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52 (br s, 1H), 11.08 (s, 1H), 8.76 (s, 1H), 8.13 (s, 1H), 7.93 (s, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.37 (d, J = 9.3 Hz, 1H), 3.00 (d, J = 1.7 Hz, 6H), 2.01-1.90 (m, 1H), 0.92-0.78 (m, 4H); LCMS(electrospray) m/z 413.0 (M + H+). H N-(6-(5-chloro-7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)cyclopropanecarboxamide 328 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.24 (br s, 1H), 11.07 (s, 1H), 8.84 (s, 1H), 8.19 (s, 1H), 8.02 (s, 1H), 7.58-7.54 (m, 1H), 7.50-7.44 (m, 2H), 5.04- 4.81 (m, 1H), 3.85 (q, J = 7.0 Hz, 2H), 2.20-2.12 (m, 1H), 1.67 (tdd, J = 3.3, 6.8, 20.0 Hz, 1H), 1.21- 1.14 (m, 1H), 1.10 (t, J = 7.0 Hz, 3H); LCMS(electrospray) m/z 398.1 (M + H+). H (1S,2S)-N-(6-(5-ethoxy-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 329 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41 (br s, 1H), 11.08 (s, 1H), 8.73 (s, 1H), 8.16 (s, 1H), 7.88 (s, 1H), 7.57 (d, J = 9.1 Hz, 1H), 7.31 (dd, J = 1.4, 9.3 Hz, 1H), 5.08-4.81 (m, 1H), 3.12 (s, 3H), 2.92 (s, 3H), 2.24 (d, J = 2.8 Hz, 3H), 2.19-2.11 (m, 1H), 1.72-1.59 (m, 1H), 1.19-1.15 (m, 1H); LCMS(electrospray) m/z 439.3 (M + H+). H 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N,N,5-trimethyl-1H-indazole-7- carboxamide 330 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 11.05 (s, 1H), 8.65 (s, 1H), 8.13 (s, 1H), 7.76 (s, 1H), 7.53 (d, J = 9.0 Hz, 1H), 7.27 (dd, J = 1.6, 9.2 Hz, 1H), 5.07-4.79 (m, 1H), 3.20 (q, J = 6.6 Hz, 2H), 2.92 (s, 3H), 2.21-2.12 (m, 4H), 1.73-1.59 (m, 1H), 1.25-1.10 (m, 1H), 1.05 (t, J = 7.1 Hz, 3H); LCMS(electrospray) m/z 424.18 (M + H+). H (1S,2S)-N-(6-(7-(ethyl(methyl)amino)-6- fluoro-5-methyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 331 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 1.12-1.22 (m, 1 H), 1.60-1.73 (m, 1 H), 2.12-2.21 (m, 1 H), 4.81- 5.05 (m, 1 H), 7.39 (dd, J = 9.26, 1.75 Hz, 1 H), 7.50 (s, 1 H) 7.58-7.64 (m, 1 H), 7.77 (s, 1 H), 8.14 (s, 1 H), 8.19 (s, 1 H), 8.87 (s, 1 H), 11.11 (s, 1 H), 13.86-13.91 (m, 1 H); LCMS(electrospray) m/z 438.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-7- (difluoromethyl)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 332 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.19 (s, 1H), 8.74 (s, 1H), 8.11 (s, 1H), 8.00-7.84 (m, 1H), 7.56 (d, J = 9.3 Hz, 1H), 7.33 (dd, J = 1.4, 9.2 Hz, 1H), 5.04-4.78 (m, 1H), 3.00 (br s, 6H), 2.46-2.41 (m, 1H), 1.61-1.44 (m, 1H), 1.25 (qd, J = 6.6, 13.1 Hz, 1H); LCMS(electrospray) m/z 431.0 (M + H+). H (1R,2S)-N-(6-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 333 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.99-13.12 (m, 1H), 11.27 (s, 1H), 8.78 (s, 1H), 8.13 (s, 1H), 7.93 (s, 1H), 7.60 (d, J = 9.3 Hz, 1H), 7.39 (d, J = 9.3 Hz, 1H), 5.05-4.75 (m, 1H), 3.00 (d, J = 2.4 Hz, 6H), 2.44 (br s, 1H), 1.63-1.46 (m, 1H), 1.26 (qd, J = 6.4, 13.2 Hz, 1H); LCMS(electrospray) m/z 431.1 (M + H+). H (1S,2R)-N-(6-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 334 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.77-13.25 (m, 1H), 11.15 (s, 1H), 8.78 (s, 1H), 8.17 (s, 1H), 7.94 (s, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.38 (d, J = 9.3 Hz, 1H), 5.09-4.80 (m, 1H), 3.00 (d, J = 2.3 Hz, 6H), 2.16 (td, J = 6.8, 13.6 Hz, 1H), 1.73-1.58 (m, 1H), 1.24-1.10 (m, 1H); LCMS(electrospray) m/z 431.1 (M + H+). H (1R,2R)-N-(6-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 335 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.34 (br s, 1H), 11.05 (s, 1H), 8.93 (s, 1H), 8.29 (s, 1H), 8.19 (s, 1H), 7.60-7.56 (m, 1H), 7.55-7.51 (m, 1H), 7.15 (d, J = 13.7 Hz, 1H), 5.06-4.80 (m, 1H), 2.95 (d, J = 1.2 Hz, 6H), 2.22-2.09 (m, 1H), 1.75-1.59 (m, 1H), 1.16 (br s, 1H); LCMS(electrospray) m/z 397.2 (M + H+). H (1S,2S)-N-(6-(7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 336 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68 (s, 1H), 11.09 (s, 1H), 8.83 (s, 1H), 8.18 (s, 1H), 8.08 (s, 1H), 7.59 (d, J = 9.2 Hz, 1H), 7.38 (dd, J = 9.0 Hz, J = 1.8 Hz, 1H), 5.03-4.83 (m, 1H), 3.84 (t, J = 6.8 Hz, 2H), 2.52 (t, J = 7.4 Hz, 2H), 2.31-2.24 (m, 2H), 2.18-2.13 (m, 1H), 1.71-1.63 (m, 1H), 1.23- 1.12 (m, 1H); LCMS (electrospray) m/z 471.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- oxopyrrolidin-1-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 337 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.62 (s, 1H), 11.06 (s, 1H), 8.82 (s, 1H), 8.16 (s, 1H), 8.11 (br, 1H), 8.08 (s, 1H), 7.59-7.55 (m, 2H), 7.38 (dd, J = 9.0 Hz, J = 1.8 Hz, 1H), 6.73 (d, J = 8.0 Hz, 1H), 6.54 (d, J = 8.0 Hz, 1H), 5.03-4.83 (m, 1H), 3.41 (s, 3H), 2.18-2.13 (m, 1H), 1.71-1.63 (m, 1H), 1.23-1.12 (m, 1H); LCMS (electrospray) m/z 494.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(pyridin-2-yl)amino)-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 338 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.22 (s, 1H), 11.07 (s, 1H), 8.79-8.65 (m, 1H), 8.46-8.34 (m, 1H), 8.17 (s, 1H), 7.90-7.78 (m, 1H), 7.65-7.51 (m, 1H), 7.36-7.22 (m, 1H), 5.08-4.78 (m, 1H), 2.89 (br d, J = 4.5 Hz, 3H), 2.24 (br d, J = 2.8 Hz, 3H), 2.19-2.13 (m, 1H), 1.74-1.58 (m, 1H), 1.23- 1.11 (m, 1H); LCMS(electrospray) m/z 425.1 (M + H+). H 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N,5-dimethyl-1H-indazole-7-carboxamide 339 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67 (br s, 1H), 11.10 (s, 1H), 8.73 (s, 1H), 8.18 (s, 1H), 7.97 (s, 1H), 7.60 (d, J = 9.1 Hz, 1H), 7.27 (dd, J = 1.6, 9.1 Hz, 1H), 5.05-4.81 (m, 1H), 2.66 (br d, J = 7.3 Hz, 2H), 2.22-2.11 (m, 1H), 1.74-1.61 (m, 1H), 1.20-1.14 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 450.2 (M + H+). H (1S,2S)-N-(6-(5-ethyl-6-fluoro-7- (trifluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 340 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (br s, 1H) 11.05 (s, 1 H) 8.94 (s, 1 H) 8.36 (br s, 1 H) 8.21 (s, 1 H) 7.52-7.62 (m, 2 H) 7.37 (br d, J = 7.25 Hz, 1 H) 7.29 (d, J = 7.50 Hz, 1 H) 4.81-5.04 (m, 1 H) 2.62 (s, 3 H) 2.12-2.20 (m, 1 H) 1.61-1.73 (m, 1 H) 1.12-1.23 (m, 1 H); LCMS(electrospray) m/z 382.1 (M + H+). H (1S,2S)-2-fluoro-N-(6-(7-(methylthio)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 341 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70 (s, 1 H), 11.06 (s, 1 H), 8.81 (s, 1 H), 8.14(s, 1 H), 8.01 (s, 1 H), 7.54 (s, 1 H), 7.37-7.34 (m, 1 H), 4.98-4.80 (m, 1 H), 3.23-3.17 (q, J = 7.0 Hz, 1H), 2.87 (s, 3 H), 2.14-2.10 (m, 1 H), 1.66-1.59 (m, 1 H), 1.16-1.10 (m, 1 H), 1.00 (t, J = 6.9 Hz, 3 H); LCMS(electrospray) m/z 473.1 (M + H+). H 5-chloro-N-ethyl-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N-methyl-1H-indazole-7-carboxamide 342 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63 (s, 1 H) 11.17 (s, 1 H) 9.07 (s, 1 H) 8.43(s, 1 H) 8.21 (s, 1 H) 7.72-7.61 (m, 2 H) 7.32 (d, J = 10.4 Hz, 1 H) 5.05-4.85 (m, 1 H) 2.51 (s, 3 H) 2.20-2.15 (m, 1 H) 1.72-1.65 (m, 1 H) 1.22-1.16 (m, 1 H); LCMS(electrospray) m/z 400.0 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- (methylthio)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)cyclopropane-1- carboxamide 343 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (s, 1H), 11.09 (s, 1H), 8.75 (s, 1H), 8.16 (s, 1H), 7.94 (d, J = 1.0 Hz, 1H), 7.73-7.43(m, 2H), 7.30 (dd, J = 1.6, 9.2 Hz, 1H), 5.10-4.79 (m, 1H), 2.24 (d, J = 2.6 Hz, 3H), 2.19-2.12 (m, 1H), 1.74-1.61 (m, 1H), 1.17 (ddd, J = 2.9, 6.2, 12.2 Hz, 1H); LCMS(electrospray) m/z 418.1 (M + H+). H (1S,2S)-N-(6-(7-(difluoromethyl)-6- fluoro-5-methyl-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 344 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.08 (br s, 1H), 11.11 (s, 1H), 9.05 (s, 1H), 8.49 (s, 1H), 8.21 (s, 1H), 7.68-7.63 (m, 1H), 7.61-7.57 (m, 1H), 7.48 (d, J = 11.6 Hz, 1H), 5.12-4.84 (m, 1H), 2.25- 2.12 (m, 1H), 1.83-1.60 (m, 1H), 1.27-1.08 (m, 1H); LCMS(electrospray) m/z 438.2 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 345 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94 (s, 1H), 11.09 (s, 1H), 8.74 (s, 1H), 8.15 (s, 1H), 7.99 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.31 (dd, J = 1.7, 9.2 Hz, 1H), 5.08-4.77 (m, 1H), 2.26 (d, J = 2.8 Hz, 3H), 2.20-2.11 (m, 1H), 1.73-1.59 (m, 1H), 1.23- 1.10 (m, 1H); LCMS(electrospray) m/z 452.3 (M + H+). H (1S,2S)-2-fluoro-N-(6-(6-fluoro-5-methyl- 7-(trifluoromethoxy)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2- yl)cyclopropane-1-carboxamide 346 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.61 (s, 1H), 11.10 (s, 1H), 8.86 (s, 1H), 8.63-8.47 (br, 2H), 8.20 (s, 1H), 8.03 (s, 1H), 7.60 (d, J = 9.6 Hz, 1H), 7.43 (t, J = 4.6 Hz, 1H), 6.86 (t, J = 6.0 Hz, 1H), 5.04- 4.83 (m, 1H), 3.53 (s, 3H), 2.20-2.13 (m, 1H), 1.72-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 495.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(pyrimidin-2-yl)amino)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 347 embedded image .sup.1H NMR (400 MHz, ACETONE-d.sub.6) δ 13.30 (s, 1H), 10.52 (s, 1H), 9.23 (s, 1H), 8.72 (s, 1H), 8.61 (s, 1H), 8.04 (d, J = 9.3 Hz, 1H), 7.90 (d, J = 9.1 Hz, 1H), 5.47-5.26 (m, 1H), 4.96-4.73 (m, 2H), 3.75 (s, 3H), 2.76-2.71 (m, 1H), 2.33-2.24 (m, 1H), 1.70-1.63 (m, 1H); LCMS(electrospray) m/z 527.1 (M + H+). H 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N-methyl-N-(2,2,2-trifluoroethyl)-1H- indazole-7-carboxamide 348 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.61 (s, 1H), 11.10 (s, 1H), 8.86 (s, 1H), 8.63 (br, 1H), 8.47 (br, 1H), 8.20 (s, 1H), 8.08 (s, 1H), 7.60 (d, J = 9.6 Hz, 1H), 7.55 (br, 1H), 7.42 (t, J = 8.0 Hz, 1H), 5.04- 4.83 (m, 1H), 3.48 (s, 3H), 2.20-2.15 (m, 1H), 1.72-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 495.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(pyrimidin-4-yl)amino)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 349 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.66 (s, 1H), 11.09 (s, 1H), 8.77 (s, 1H), 8.59 (s, 1H), 8.46 (s, 1H), 8.20 (s, 1H), 7.96 (s, 1H), 7.82 (d, J = 6.8 Hz, 1H), 7.56 (d, J = 8.8 Hz, 1H), 7.34 (t, J = 8.2 Hz, 2H), 5.04-4.83 (m, 1H), 4.45 (s, 2H), 2.90 (s, 3H), 2.20-2.15 (m, 1H), 1.72-1.62 (m, 1H), 1.23- 1.13 (m, 1H); LCMS (electrospray) m/z 508.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(pyridin-3-ylmethyl)amino)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 350 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.18-13.20 (m, 1H), 11.22 (s, 1H), 8.74 (d, J = 7.2 Hz, 1H), 8.15 (s, 1H), 7.89 (s, 1H), 7.10-6.94 (m, 2H), 5.16-4.74 (m, 1H), 4.12 (s, 3H), 2.25-2.09 (m, 1H), 1.78-1.54 (m, 1H), 1.29-1.05 (m, 1H); LCMS(electrospray) m/z 470.2 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- methyl-1H-tetrazol-5-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 351 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.75-14.36 (m, 1H), 11.13 (s, 1H), 8.90 (s, 1H), 8.27 (s, 1H), 8.21 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.41 (dd, J = 1.5, 9.3 Hz, 1H), 5.09-4.80 (m, 1H), 2.22-2.13 (m, 1H), 1.74-1.59 (m, 1H), 1.12-1.20 (m, J = 2.9, 6.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 413.2 (M + H+). H (1S,2S)-N-(6-(5-chloro-7-cyano-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 352 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.25-13.17 (m, 1H), 11.02 (s, 1H), 8.84 (s, 1H), 8.31-8.24 (m, 1H), 8.18 (s, 1H), 7.57-7.50 (m, 2H), 7.16 (d, J = 7.6 Hz, 1H), 6.80 (br d, J = 3.8 Hz, 1H), 5.07-4.78 (m, 1H), 2.92 (br s, 6H), 2.23-2.09 (m, 1H), 1.76- 1.58 (m, 1H), 1.27-1.08 (m, 1H); LCMS(electrospray) m/z 379.1 (M + H+). H (1S,2S)-N-(6-(7-(dimethylamino)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 353 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69 (s, 1H), 11.08 (s, 1H), 8.76 (s, 1H), 8.52 (s, 2H), 8.15 (s, 1H), 7.97 (s, 1H), 7.54 (s, 1H), 7.46 (s, 2H), 7.33 (br, 1H), 5.04-4.83 (m, 1H), 4.48 (s, 2H), 2.91 (s, 3H), 2.20-2.15 (m, 1H), 1.72-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 508.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methyl(pyridin-4-ylmethyl)amino)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 354 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (s, 1H), 11.10 (s, 1H), 8.71 (s, 1H), 8.20 (s, 1H), 8.09 (s, 1H), 7.52 (t, J = 9.7 Hz, 2H), 7.28 (td, J = 2.4, 8.9 Hz, 1H), 5.05-4.80 (m, 1H), 2.85 (s, 3H), 2.72 (s, 3H), 2.16 (br s, 1H), 1.74-1.58 (m, 1H), 1.23-1.12 (m, 1H); LCMS(electrospray) m/z 425.2 (M + H+). H 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N,N-dimethyl-1H-indazole-7-carboxamide 355 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (s, 1H), 11.10 (s, 1H), 8.71 (s, 1H), 8.20 (s, 1H), 8.09 (s, 1H), 7.52 (t, J = 9.7 Hz, 2H), 7.28 (td, J = 2.4, 8.9 Hz, 1H), 5.05-4.80 (m, 1H), 2.85 (s, 3H), 2.72 (s, 3H), 2.16 (br s, 1H), 1.74-1.58 (m, 1H), 1.23-1.12 (m, 1H); LCMS(electrospray) m/z 425.2 (M + H+). H 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- N,N-dimethyl-1H-indazole-5-carboxamide 356 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.98 (s, 1H), 11.08 (s, 1H), 8.81 (s, 1H), 8.23-8.18 (m, 2H), 7.55 (d, J = 8.8 Hz, 1H), 7.42 (d, J = 8.8 Hz, 1H), 5.03-4.82 (m, 1H), 3.88 (q, J = 7.0 Hz, 2H), 2.17- 2.14 (m, 1H), 1.70-1.63 (m, 1H), 1.19-1.16 (m, 1H), 1.10 (t, J = 7.0 Hz, 3H); LCMS(electrospray) m/z 416.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 357 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.98 (s, 1H), 11.08 (s, 1H), 8.81 (s, 1H), 8.23-8.18 (m, 2H), 7.55 (d, J = 8.8 Hz, 1H), 7.42 (d, J = 8.8 Hz, 1H), 5.03-4.82 (m, 1H), 3.88 (q, J = 7.0 Hz, 2H), 2.17- 2.14 (m, 1H), 1.70-1.63 (m, 1H), 1.19-1.16 (m, 1H), 1.10 (t, J = 7.0 Hz, 3H); LCMS(electrospray) m/z 416.1 (M + H+). H (1S,2S)-N-(6-(5-ethoxy-6,7-difluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 358 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64 (s, 1H), 11.12 (s, 1H), 8.83 (s, 1H), 8.18 (s, 1H), 8.03 (s, 1H), 7.59 (d, J = 9.6 Hz, 1H), 7.38 (dd, J = 1.6, 9.2 Hz, 1H), 5.03-4.84 (m, 1H), 3.83 (t, J = 7.8 Hz, 2H), 3.60 (t, J = 8.0 Hz, 2H), 2.82 (s, 3H), 2.16 (m, 1H), 1.69-1.64 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 486.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(3- methyl-2-oxoimidazolidin-1-yl)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 359 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26 (s, 1H), 11.08 (s, 1H), 8.73 (s, 1H), 8.14 (s, 1H), 7.90 (s, 1H), 7.53 (d, J = 9.2 Hz, 1H), 7.32 (dd, J = 1.6, 9.2 Hz, 1 H), 5.16 (dd, J = 2.6, 9.8 Hz, 1H), 5.03-4.83 (m, 1H), 4.08 (s, 1H), 2.19-2.12 (m, 1H), 1.71- 1.61 (m, 1H), 1.22 (d, J = 6.8 Hz, 6H), 1.19-1.12 (m, 1H); LCMS (electrospray) m/z 445.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (isopropylamino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 360 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 11.11 (s, 1H), 8.78 (s, 1H), 8.16 (s, 1H), 7.95 (s, 1H), 7.56 (d, J = 9.2 Hz, 1H), 7.36 (dd, J = 1.8, 9.4 Hz, 1H), 5.02-4.85 (m, 1H), 3.54 (s, 1H), 2.89 (d, J = 3.2 Hz, 3H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.21-1.13 (m, 7H); LCMS (electrospray) m/z 459.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (isopropyl(methyl)amino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 361 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 11.10 (s, 1H), 8.77 (s, 1H), 8.15 (s, 1H), 7.92 (s, 1H), 7.56 (d, J = 8.8 Hz, 1H), 7.35 (dd, J = 9.2 Hz, J = 2.0 Hz, 1H), 5.03-4.83 (m, 1H), 3.01-2.98 (br, 4H), 2.17-2.14 (m, 1H), 1.69-1.62 (m, 1H), 1.19-1.14 (m, 1H) 0.64-0.59 (m, 2H), 0.48-0.45 (m, 2H); LCMS (electrospray) m/z 457.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- (cyclopropyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 362 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (s, 1H), 11.10 (s, 1H), 8.81 (s, 1H), 8.18 (s, 1H), 7.96 (d, J = 1.6 Hz, 1H), 7.58 (d, J = 9.6 Hz, 1H), 7.35 (dd, J = 1.6, 9.2 Hz, 1H), 5.47 (t, J = 5.6 Hz, 1H), 5.03- 4.83 (m, 3H), 2.19-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.19-1.12 (m, 1H); LCMS (electrospray) m/z 419.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (hydroxymethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 363 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.90 (s, 1H), 11.12 (s, 1H), 8.85 (s, 1H), 8.18 (s, 1H), 8.07 (d, J = 1.2 Hz, 1H), 7.59 (d, J = 9.6 Hz, 1H), 7.38 (dd, J = 2.0, 9.2 Hz, 1H), 5.93 (s, 1H), 5.81 (s, 1H), 5.04- 4.83 (m, 1H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.19-1.13 (m, 1H); LCMS (electrospray) m/z 420.05 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (fluoromethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 364 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.73 (s, 1H), 11.15 (s, 1H), 8.93 (s, 1H), 8.23 (s, 1H), 8.21 (s, 1H), 7.63 (d, J = 9.2 Hz, 1H), 7.45 (d, J = 9.2 Hz, 1H), 5.03-4.84 (m, 1H), 2.55 (s, 3H), 2.16-2.14 (m, 1H), 1.69-1.63 (m, 1H), 1.20-1.15 (m, 1H); LCMS (electrospray) m/z 470.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(3- methyl-1,2,4-oxadiazol-5-yl)-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 365 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56-14.07 (1H), 11.12 (s, 1H), 8.84 (d, J = 1.1 Hz, 1H), 8.20 (s, 1H), 8.17 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 9.1, 1.9 Hz, 1H), 7.28 (s, 2H), 6.41 (t, J = 2.2 Hz, 2H), 5.04-4.84 (m, 1H), 2.20-2.13 (m, 1H), 1.70-1.64 (m, 1H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 453.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1H- pyrrol-1-yl)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 366 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 11.09 (s, 1H), 8.77 (s, 1H), 8.14 (s, 1H), 7.97 (s, 1H), 7.54 (d, J = 8.8 Hz, 1H), 7.35 (dd, J = 9.3, 1.6 Hz, 1H), 6.79-6.22 (m, 1H), 5.10-4.47 (m, 3H), 2.25-2.09 (m, 1H), 1.76-1.57 (m, 1H), 1.21-1.09 (m, 1H); LCMS (electrospray) m/z 442.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- ((cyanomethyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 367 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.03 (s, 1H), 11.07 (s, 1H), 8.71 (s, 1H), 8.16 (d, J = 13.2 Hz, 1H), 7.86 (s, 1H), 7.53 (d, J = 9.3 Hz, 1H), 7.30 (dd, J = 8.8, 1.6 Hz, 1H), 6.08 (s, 1H), 5.09-4.81 (m, 1H), 3.12 (s, 1H), 2.17-2.08 (m, 1H), 1.66 (d, J = 23.1 Hz, 1H), 1.23-1.14 (m, 1H), 0.80 (d, J = 5.5 Hz, 2H), 0.63 (d, J = 3.3 Hz, 2H); LCMS(electrospray) m/z 443.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-7- (cyclopropylamino)-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 368 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.96 (s, 1H), 11.12 (s, 1H), 8.93-8.83 (m, 1H), 8.17-8.12 (m, 2H), 7.69-7.57 (m, 1H), 7.46-7.36 (m, 1H), 5.04- 4.83 (m, 1H), 3.44 (qd, J = 7.2, 3.7 Hz, 1H), 2.19- 2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.23-1.13 (m, 1H), 0.98-0.55 (m, 4H); LCMS(electrospray) m/z 539.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-7-(N-cyclopropyl- 2,2,2-trifluoroacetamido)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 369 05embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16 (s, 1H), 11.11 (s, 1H), 10.16 (s, 1H), 8.83 (d, J = 1.1 Hz, 1H), 8.18 (s, 1H), 7.98 (d, J = 1.6 Hz, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 4.93 (ddd, J = 66.2, 9.9, 6.3 Hz, 1H), 4.76 (t, J = 5.5 Hz, 1H), 3.79 (q, J = 6.2 Hz, 2H), 2.65 (t, J = 6.6 Hz, 2H), 2.19-2.08 (m, 1H), 1.70-1.61 (m, 1H), 1.23- 1.13 (m, 1H); LCMS(electrospray) m/z 475.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(3- hydroxypropanamido)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 370 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.12-13.48 (1H), 11.08 (s, 1H), 8.72 (s, 1H), 8.14 (s, 1H), 7.90 (s, 1H), 7.52 (d, J = 9.3 Hz, 1H), 7.31 (dd, J = 9.1, 1.9 Hz, 1H), 5.16 (d, J = 6.9 Hz, 1H), 5.03-4.83 (m, 1H), 3.90 (s, 1H), 2.19-2.12 (m, 1H), 1.71- 1.58 (m, 2H), 1.53-1.46 (m, 1H), 1.23-1.12 (m, 4H), 0.94 (t, J = 7.4 Hz, 3H); LCMS (electrospray) m/z 459.10 (M + H)+. H (1S,2S)-N-(6-(7-(sec-butylamino)-5- chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 371 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 11.10 (s, 1H), 8.77 (d, J = 12.6 Hz, 1H), 8.14 (d, J = 8.2 Hz, 1H), 7.97 (s, 1H), 7.54 (t, J = 9.3 Hz, 1H), 7.35 (d, J = 9.3 Hz, 1H), 6.66-6.46 (m, 0.5H), 6.11 (d, J = 9.3 Hz, 1H), 5.99-5.80 (m, 0.5H), 5.10-4.77 (m, 2H), 2.24-2.09 (m, 1H), 1.81-1.58 (m, 4H), 1.21-1.06 (m, 1H); LCMS (electrospray) m/z 456.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((1- cyanoethyl)amino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 372 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.28 (s, 1H), 11.11 (s, 1H), 8.80 (t, J = 1.4 Hz, 1H), 8.18 (s, 1H), 7.94 (d, J = 1.6 Hz, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 9.1, 1.9 Hz, 1H), 5.83 (d, J = 3.8 Hz, 1H), 5.43-5.37 (m, 1H), 5.04-4.83 (m, 1H), 2.19- 2.12 (m, 1H), 1.70-1.62 (m, 1H), 1.54 (d, J = 6.6 Hz, 3H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 433.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- hydroxyethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 373 09embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 11.11 (s, 1H), 8.82 (t, J = 1.4 Hz, 1H), 8.17 (s, 1H), 7.99 (s, 1H), 7.61-7.57 (m, 1H), 7.38 (dd, J = 9.3, 1.6 Hz, 1H), 5.07-4.83 (m, 2H), 3.23 (s, 3H), 2.19- 2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.57 (t, J = 6.3 Hz, 4H), 1.21-1.13 (m, 2H); LCMS (electrospray) m/z 447.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- methoxyethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 374 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68 (s, 1H), 11.11 (s, 1H), 8.83 (t, J = 1.4 Hz, 1H), 8.18 (s, 1H), 8.05 (s, 1H), 7.61-7.58 (m, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 6.43-6.27 (m, 1H), 5.04-4.83 (m, 1H), 2.20-2.13 (m, 1H), 1.83 (dd, J = 23.9, 6.3 Hz, 3H), 1.72-1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 435.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- fluoroethyl)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 375 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.37 (s, 1H), 11.44 (s, 1H), 11.11 (s, 1H), 8.82 (d, J = 1.1 Hz, 1H), 8.18 (s, 1H), 8.01 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.49 (s, 1H), 7.39 (dd, J = 9.1, 1.9 Hz, 1H), 7.01 (s, 1H), 6.68 (s, 1H), 5.04-4.84 (m, 1H), 2.20- 2.13 (m, 1H), 1.71-1-61 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 454.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1H- pyrrol-3-yl)-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 376 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 11.11 (s, 1H), 8.82 (d, J = 1.6 Hz, 1H), 8.18 (s, 1H), 8.01 (s, 1H), 7.58 (d, J = 8.8 Hz, 1H), 7.46 (s, 1H), 7.38 (dd, J = 9.1, 1.9 Hz, 1H), 6.96 (s, 1H), 6.64 (s, 1H), 5.04-4.83 (m, 1H), 3.75 (s, 3H), 2.20-2.13 (m, 1H), 1.71-1.61 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 468.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- methyl-1H-pyrrol-3-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 377 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (s, 1H), 11.12 (s, 1H), 8.87 (t, J = 1.4 Hz, 1H), 8.19 (s, 1H), 8.04 (s, 1H), 7.60 (d, J = 9.3 Hz, 1H), 7.42 (dd, J = 9.1, 1.9 Hz, 1H), 7.08 (s, 1H), 6.39-6.37 (m, 1H), 6.26 (t, J = 3.0 Hz, 1H), 5.04-4.84 (m, 1H), 3.54 (d, J = 1.1 Hz, 3H), 2.20-2.13 (m, 1H), 1.72-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 468.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- methyl-1H-pyrrol-2-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 378 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.57 (s, 1H), 11.12 (s, 1H), 8.88 (t, J = 1.1 Hz, 1H), 8.21 (s, 1H), 8.10 (s, 1H), 7.70 (d, J = 1.6 Hz, 1H), 7.62 (d, J = 9.3 Hz, 1H), 7.43 (dd, J = 9.1, 1.9 Hz, 1H), 6.64 (d, J = 1.4 Hz, 1H), 5.04-4.84 (m, 1H), 3.76 (s, 3H), 2.20-2.13 (m, 1H), 1.71-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 469.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- methyl-1H-pyrazol-5-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 379 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94 (s, 1H), 11.11 (s, 1H), 9.01 (s, 1H), 8.86 (s, 1H), 8.17 (s, 1H), 8.09 (s, 1H), 7.59 (d, J = 9.1 Hz, 1H), 7.39 (dd, J = 9.2, 1.5 Hz, 1H), 6.36 (s, 2H), 5.02-4.85 (m, 1H), 2.18-2.14 (m, 1H), 1.70-1.63 (m, 1H), 1.20-1.14 (m, 1H); LCMS (electrospray) m/z 470.10 (M + H)+. I (1S,2S)-N-(6-(7-((2H-tetrazol-2- yl)methyl)-5-chloro-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 380 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.56 (s, 1H), 11.10 (s, 1H), 8.82 (d, J = 1.1 Hz, 1H), 8.17 (s, 1H), 7.96 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.36 (dd, J = 9.1, 1.9 Hz, 1H), 5.04-4.83 (m, 1H), 3.91 (d, J = 1.1 Hz, 2H), 3.20 (q, J = 6.8 Hz, 4H), 2.19-2.12 (m, 1H), 2.00-1.93 (m, 2H), 1.71-1.61 (m, 1H), 1.23- 1.13 (m, 1H); LCMS (electrospray) m/z 457.10 (M + H)+. H (1S,2S)-N-(6-(7-(azetidin-1-ylmethyl)-5- chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 381 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (s, 1H), 11.11 (s, 1H), 8.82 (d, J = 1.1 Hz, 1H), 8.18 (s, 1H), 7.98 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.84 (m, 1H), 4.00 (d, J = 1.1 Hz, 2H), 2.53-2.49 (m, 4H), 2.20-2.13 (m, 1H), 1.70-1.62 (m, 5H), 1.24-1.13 (m, 1H); LCMS (electrospray) m/z 472.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (pyrrolidin-1-ylmethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 382 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 11.11 (s, 1H), 8.83 (t, J = 1.1 Hz, 1H), 8.17 (s, 1H), 7.97 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.38 (dd, J = 9.1, 1.9 Hz, 1H), 5.04-4.83 (m, 1H), 3.84 (s, 2H), 2.44 (s, 4H), 2.19-2.12 (m, 1H), 1.70-1.62 (m, 1H), 1.51-1.37 (m, 6H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 486.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (piperidin-1-ylmethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 383 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.92 (s, 1H), 11.11 (s, 1H), 8.85 (d, J = 1.1 Hz, 1H), 8.17 (s, 1H), 8.07 (s, 1H), 7.81 (s, 2H), 7.58 (d, J = 9.3 Hz, 1H), 7.38 (dd, J = 9.1, 1.9 Hz, 1H), 6.07 (s, 2H), 5.04- 4.83 (m, 1H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 469.10 (M + H)+. I (1S,2S)-N-(6-(7-((2H-1,2,3-triazol-2- yl)methyl)-5-chloro-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 384 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.95 (s, 1H), 11.11 (s, 1H), 8.83 (t, J = 1.4 Hz, 1H), 8.31 (d, J = 1.4 Hz, 1H), 8.17 (s, 1H), 8.09 (s, 1H), 7.75 (d, J = 1.1 Hz, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 6.03 (s, 2H), 5.04-4.83 (m, 1H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 469.10 (M + H)+. I (1S,2S)-N-(6-(7-((1H-1,2,3-triazol-1- yl)methyl)-5-chloro-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 385 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.92 (s, 1H), 11.11 (s, 1H), 8.83 (d, J = 1.1 Hz, 1H), 8.79 (s, 1H), 8.16 (s, 1H), 8.07 (s, 1H), 7.96 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 5.83 (s, 2H), 5.04-4.83 (m, 1H), 2.19-2.12 (m, 1H), 1.71- 1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 469.10 (M + H)+. I (1S,2S)-N-(6-(7-((1H-1,2,4-triazol-1- yl)methyl)-5-chloro-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 386 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.86 (s, 1H), 11.12 (s, 1H), 8.85 (s, 1H), 8.17 (s, 1H), 8.08 (s, 1H), 7.58 (d, J = 9.6 Hz, 1H), 7.38 (dd, J = 9.3, 1.6 Hz, 1H), 7.33 (d, J = 1.1 Hz, 1H), 6.93-6.91 (m, 1H), 5.04-4.83 (m, 1H), 3.80 (d, J = 15.4 Hz, 3H), 2.19-2.12 (m, 1H), 1.70-1.62 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 501.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((1- methyl-1H-imidazol-2-yl)thio)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 387 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.20-13.84 (s, 1 H) 8.84 (s, 1 H) 8.71 (d, J = 9.4 Hz, 1 H) 7.92 (s, 1 H) 7.87 (s, 1 H) 7.49 (d, J = 9.13 Hz, 1 H) 7.27 (dd, J = 9.26, 1.75 Hz, 1 H) 6.87 (br s, 1 H) 3.00 (d, J = 2.38 Hz, 6 H) 2.66-2.70 (m, 1 H) 0.61-0.71 (m, 2 H) 0.39-0.46 (m, 2 H); LCMS (electrospray) m/z 428.1 (M + H+). H 1-(6-(5-chloro-7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-3-cyclopropylurea 388 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.12 (s, 1H), 8.89 (s, 1H), 8.21 (s, 1H), 8.15 (s, 1H), 7.62 (d, J = 9.2 Hz, 1H), 7.44 (dd, J = 1.6, 9.3 Hz, 1H), 6.95 (br s, 1H), 6.27 (t, J = 3.1 Hz, 1H), 6.14 (br s, 1H), 5.13-4.80 (m, 1H), 2.18 (td, J = 7.0, 13.9 Hz, 1H), 2.07 (s, 3H), 1.74-1.61 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 467.1 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- methyl-1H-pyrrol-1-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 389 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70-11.96 (m, 1H), 11.08 (s, 1H), 8.79 (s, 1H), 8.17 (s, 1H), 7.89 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.35 (dd, J = 1.7, 9.2 Hz, 1H), 6.56-5.57 (m, 1H), 5.21-4.65 (m, 1H), 2.25-2.09 (m, 1H), 1.69 (d, J = 1.4 Hz, 6H), 1.65-1.59 (m, 1H), 1.17 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 446.0 (M + H+). H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- hydroxypropan-2-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 390 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.66 (s, 1H), 11.11 (s, 1H), 8.83 (s, 1H), 8.18 (s, 1H), 8.00 (d, J = 1.1 Hz, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 5.04-4.83 (m, 3H), 3.36 (s, 3H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 432.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (methoxymethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 391 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.65 (s, 1H), 11.11 (s, 1H), 8.83 (d, J = 1.1 Hz, 1H), 8.18 (s, 1H), 8.00 (d, J = 1.6 Hz, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 3H), 3.57 (q, J = 7.1 Hz, 2H), 2.19-2.12 (m, 1H), 1.66 (dtd, J = 23.3, 6.7, 3.5 Hz, 1H), 1.39 (s, 0H), 1.24- 1.13 (m, 4H); LCMS (electrospray) m/z 446.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(ethoxymethyl)- 6-fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 392 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76-14.21 (1H), 11.11 (s, 1H), 9.64 (s, 1H), 8.84 (s, 1H), 8.17 (s, 1H), 8.09 (s, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.38 (d, J = 8.8 Hz, 1H), 6.11 (s, 2H), 5.01-4.85 (m, 1H), 2.19-2.12 (m, 1H), 1.69-1.63 (m, 1H), 1.19- 1.13 (m, 1H); LCMS (electrospray) m/z 470.10 (M + H)+. I (1S,2S)-N-(6-(7-((1-tetrazol-1- yl)methyl)-5-chloro-6-fluoro-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 393 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54-13.94 (s, 1H), 11.06 (d, J = 7.7 Hz, 1H), 8.98 (d, J = 11.5 Hz, 1H), 8.80 (s, 1H), 8.12 (s, 2H), 7.58-7.54 (m, 1H), 7.35 (dd, J = 9.3, 1.6 Hz, 1H), 6.74 (q, J = 7.1 Hz, 1H), 5.00-4.79 (m, 1H), 2.24-2.20 (m, 3H), 2.16- 2.09 (m, 1H), 1.68-1.57 (m, 1H), 1.18-1.09 (m, 1H); LCMS (electrospray) m/z 485.10 (M + H)+. I (1S,2S)-N-(6-(7-(1-(2H-tetrazol-2- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 394 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (s, 1H), 11.06 (d, J = 6.6 Hz, 1H), 8.71 (d, J = 7.7 Hz, 1H), 8.13 (d, J = 7.7 Hz, 1H), 7.88 (d, J = 1.1 Hz, 1H), 7.52 (t, J = 8.5 Hz, 1H), 7.31 (dd, J = 9.3, 1.6 Hz, 1H), 5.56-5.52 (m, 1H), 5.03-4.82 (m, 2H), 3.09 (s, 3H), 2.85 (s, 3H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.34 (d, J = 6.6 Hz, 3H), 1.21-1.12 (m, 1H); LCMS (electrospray) m/z 503.15 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((1- (dimethylamino)-1-oxopropan-2- yl)amino)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 395 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.01 (s, 1H), 11.09 (s, 1H), 8.81 (s, 1H), 8.16 (s, 1H), 7.94 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 1.7, 9.3 Hz, 1H), 5.08-4.80 (m, 1H), 3.18 (s, 3H), 2.15 (br d, J = 7.0 Hz, 1H), 1.71 (br d, J = 2.7 Hz, 6H), 1.64 (br s, 1H), 1.17 (br dd, J = 8.9, 12.1 Hz, 1H); LCMS (electrospray) m/z 460.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- methoxypropan-2-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 396 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.37-12.98 (m, 1H), 11.09 (s, 1H), 8.82 (s, 1H), 8.22 (s, 1H), 8.16 (s, 1H), 7.95 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.37 (dd, J = 1.7, 9.2 Hz, 1H), 5.03-4.82 (m, 1H), 3.87 (q, J = 6.6 Hz, 1H), 2.21 (s, 6H), 2.16 (br dd, J = 6.1, 7.6 Hz, 1H), 1.72-1.61 (m, 1H), 1.49 (d, J = 6.8 Hz, 3H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 459.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1- (dimethylamino)ethyl)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. Formaic acid salt 397 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26-13.88 (1H), 11.08 (s, 1H), 8.71 (d, J = 1.6 Hz, 1H), 8.15 (s, 1H), 7.94 (s, 1H), 7.53 (d, J = 9.3 Hz, 1H), 7.30 (dd, J = 9.3, 1.6 Hz, 1H), 5.75 (d, J = 3.3 Hz, 1H), 5.03-4.83 (m, 1H), 4.42 (d, J = 4.4 Hz, 2H), 3.02 (s, 3H), 2.88 (s, 3H), 2.19-2.12 (m, 1H), 1.71-1.61 (m, 1H), 1.23-1.12 (m, 1H); LCMS (electrospray) m/z 488.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((2- (dimethylamino)-2-oxoethyl)amino)-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 398 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53-14.00 (1H), 11.12 (s, 1H), 9.77 (s, 1H), 8.83 (s, 1H), 8.20- 8.17 (m, 2H), 7.59 (d, J = 9.1 Hz, 1H), 7.38 (dd, J = 9.3, 1.6 Hz, 1H), 6.59 (q, J = 7.1 Hz, 1H), 5.04- 4.83 (m, 1H), 2.21 (d, J = 7.1 Hz, 3H), 2.17-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 484.10 (M + H)+. I (1S,2S)-N-(6-(7-(1-(1H-tetrazol-1- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 399 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.10 (s, 1H), 8.79 (s, 1H), 8.20 (d, J = 15.8 Hz, 2H), 8.00 (s, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.34 (dd, J = 1.8, 9.2 Hz, 1H), 5.03-4.84 (m, 1H), 4.81-4.75 (m, 1H), 2.22- 2.09 (m, 1H), 1.75-1.59 (m, 1H), 1.54 (d, J = 6.8 Hz, 3H), 1.27-1.12 (m, 1H); LCMS (electrospray) m/z 431.1 (M + H)+. H (1S,2S)-N-(6-(7-(1-aminoethyl)-5-chloro- 6-fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 400 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.12-13.82 (m, 1H), 11.11 (s, 1H), 8.84 (s, 1H), 8.27-8.14 (m, 1H), 7.64 (s, 1H), 7.61 (d, J = 9.2 Hz, 1H), 7.39 (dd, J = 9.1, 1.8 Hz, 1H), 7.27 (s, 1H), 6.66 (dd, J = 2.9, 1.6 Hz, 1H) 5.10-4.79 (m, 1H), 3.22-3.00 (m, 6H), 2.21-2.12 (m, 1H), 1.74-1.61(m, 1H), 1.24-1.12 (m, 1H); LCMS (electrospray) m/z 524.1 (M + H)+. H 1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazol-7-yl)-N,N-dimethyl-1H- pyrrole-3-carboxamide 401 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.79 (s, 1 H) 11.18 (s, 1 H) 8.67 (d, J = 7.09 Hz, 1 H) 7.93 (s, 1 H) 7.77 (s, 1 H) 6.92-6.99 (m, 2 H) 4.82-5.08 (m, 1 H) 4.53 (s, 1 H) 2.15 (m, 1 H) 1.61-1.75 (m, 1 H) 1.12-1.27 (m, 1 H) 0.92 (br s, 2 H) 0.68- 0.77 (m, 2 H); LCMS (electrospray) m/z 444.0 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-cyclopropoxy-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 402 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.08 (s, 1H), 8.81 (s, 1H), 8.27 (br s, 1H), 8.16 (s, 1H), 7.96 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 1.7, 9.3 Hz, 1H), 5.12-4.75 (m, 1H), 4.33 (d, J = 6.8 Hz, 1H), 2.22-2.12 (m, 4H), 1.74-1.59 (m, 1H), 1.47 (d, J = 6.7 Hz, 3H), 1.22-1.12 (m, 1H); LCMS (electrospray) m/z 445.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (methylamino)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 403 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35-13.11 (m, 1H), 10.33 (s, 1H), 8.40 (s, 1H), 7.96-7.72 (m, 1H), 7.44 (s, 2H), 6.36 (d, J = 1.4 Hz, 1H), 5.79 (s, 2H), 5.09 (dd, J = 2.4, 9.4 Hz, 1H), 5.05-4.81 (m, 1H), 4.17-3.92 (m, 1H), 4.14-2.74 (m, 1H), 2.17- 2.05 (m, 1H), 1.71-1.55 (m,12H), 1.23 (d, J = 6.3 Hz, 6H), 1.21-1.08 (m, 1H); LCMS (electrospray) m/z 460.2 (M + H)+. H (1S,2S)-N-(8-amino-6-(5-chloro-6-fluoro- 7-(isopropylamino)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 formic acid 404 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.17-13.33 (m, 1H), 11.08 (s, 1H), 8.79 (s, 1H), 8.16 (s, 1H), 8.00 (s, 1H), 7.56 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 1.5, 9.2 Hz, 1H), 5.06-4.81 (m, 1H), 4.73 (br d, J = 1.1 Hz, 1H), 2.16 (td, J = 6.9, 13.8 Hz, 1H), 2.07 (s, 1H), 1.76-1.56 (m, 1H), 1.37 (d, J = 6.0 Hz, 6H), 1.17 (tdd, J = 6.2, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z 446.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- isopropoxy-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 405 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (br s, 1H), 11.08 (s, 1H), 8.78 (d, J = 1.0 Hz, 1H), 8.16 (s, 1H), 7.96 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 1.8, 9.3 Hz, 1H), 5.05-4.80 (m, 1H), 3.67-3.55 (m, 1H), 2.16 (td, J = 7.0, 14.0 Hz, 1H), 1.73-1.59 (m, 1H), 1.45 (d, J = 7.0 Hz, 6H), 1.17 (tdd, J = 6.1, 9.1, 12.1 Hz, 1H); LCMS (electrospray) m/z 430.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- isopropyl-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 406 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (s, 1H), 11.11 (s, 1H), 8.79 (s, 1H), 8.17 (s, 1H), 7.96 (d, J = 1.1 Hz, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 1H), 3.61 (q, J = 8.8 Hz, 1H), 2.19-1.91 (m, 8H), 1.73-1.61 (m, 3H), 1.24-1.07 (m, 1H); LCMS (electrospray) m/z 456.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-cyclopentyl-6- fluoro-1H-indazol-4-yl)imidazo[1,2- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 407 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.18-13.49 (m, 1H), 11.09 (s, 1H), 9.02 (s, 1H), 8.83 (s, 1H), 8.28-7.99 (m, 2H), 7.58 (d, J = 9.2 Hz, 1H), 7.38 (dd, J = 1.7, 9.2 Hz, 1H), 6.78 (q, J = 6.9 Hz, 1H), 5.10-4.74 (m, 1H), 2.27 (d, J = 7.0 Hz, 3H), 2.21- 2.11 (m, 1H), 1.74-1.59 (m, 1H), 1.22-1.12 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. I (1S,2S)-N-(6-(7-((R)-1-(2H-tetrazol-2- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 408 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.19-13.48 (m, 1H), 11.09 (s, 1H), 9.02 (s, 1H), 8.83 (s, 1H), 8.31-7.98 (m, 2H), 7.59 (d, J = 9.2 Hz, 1H), 7.38 (dd, J = 1.7, 9.2 Hz, 1H), 6.78 (q, J = 7.1 Hz, 1H), 5.09-4.68 (m, 1H), 2.27 (d, J = 7.0 Hz, 3H), 2.20- 2.10 (m, 1H), 1.67 (tdd, J = 3.2, 6.8, 19.9 Hz, 1H), 1.23-1.13 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. I (1S,2S)-N-(6-(7-((S)-1-(2H-tetrazol-2- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 409 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 11.10 (s, 1H), 8.86 (s, 1H), 8.17 (s, 1H), 8.01 (d, J = 1.6 Hz, 1H), 7.59 (q, J = 9.7 Hz, 2H), 7.40 (dd, J = 9.3, 1.6 Hz, 1H), 5.82-5.75 (m, 1H), 5.04-4.83 (m, 1H), 2.20-2.13 (m, 1H), 1.72-1.62 (m, 1H), 1.28-1.11 (m, 1H); LCMS (electrospray) m/z 487.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2- trifluoro-1-hydroxyethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 410 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 11.08 (s, 1H), 8.77 (s, 1H), 8.18 (s, 1H), 7.95 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.34 (dd, J = 9.3, 1.6 Hz, 1H), 5.03-4.83 (m, 2H), 4.50-4.42 (m, 3H), 3.51-3.38 (m, 6H), 2.20-2.07 (m, 3H), 1.99-1.83 (m, 3H), 1.72-1.61 (m, 2H), 1.23-1.13 (m, 4H); LCMS (electrospray) m/z 472.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- hydroxycyclopentyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 411 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 8.62-8.72 (m, 1 H) 8.12-8.25 (m, 1 H) 7.83-7.96 (m, 1 H) 7.56- 7.62 (m, 1 H) 7.43-7.52 (m, 1 H) 4.95-4.98 (m, 0.5 H) 4.77-4.81 (m, 0.5 H) 2.70-2.80 (m, 3 H) 2.07-2.17 (m, 1H) 1.73-1.88 (m, 1 H) 1.18-1.31 (m, 1 H); LCMS (electrospray) m/z 461.3 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- ethanethioamido-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 412 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54-12.76 (m, 1H), 11.09 (s, 1H), 8.80 (s, 1H), 8.36 (s, 1H), 8.17 (s, 1H), 8.07-7.97 (m, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.36 (br d, J = 9.0 Hz, 1H), 7.23 (br d, J = 6.8 Hz, 1H), 6.87 (br d, J = 5.0 Hz, 1H), 6.07 (q, J = 6.7 Hz, 1H), 5.82-5.67 (m, 1H), 5.13-4.80 (m, 1H), 3.02 (s, 3H), 2.78 (br s, 1H), 2.20-2.14 (m, 1H), 2.10-2.00 (m, 3H), 1.86-1.75 (m, 1H), 1.71- 1.64 (m, 3H), 1.28-1.07 (m, 1H); LCMS (electrospray) m/z 487.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1-(N- methylacetamido)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 413 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.10 (s, 1H), 9.77 (s, 1H), 8.82 (s, 1H), 8.24-8.00 (m, 2H), 7.58 (d, J = 9.1 Hz, 1H), 7.37 (dd, J = 1.6, 9.3 Hz, 1H), 6.62 (d, J = 7.4 Hz, 1H), 5.11-4.74 (m, 1H), 2.25- 2.15 (m, 4H), 1.79-1.56 (m, 1H), 1.27-1.10 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. I (1S,2S)-N-(6-7-((R)-1-(1H-tetrazol-1- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 414 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.75 (br s, 1H), 11.09 (s, 1H), 9.75 (s, 1H), 8.82 (s, 1H), 8.17 (s, 1H), 8.08 (s, 1H), 7.59 (br d, J = 8.9 Hz, 1H), 7.37 (dd, J = 1.7, 9.2 Hz, 1H), 6.59 (br d, J = 6.8 Hz, 1H), 5.12-4.75 (m, 1H), 2.26-2.07 (m, 4H), 1.75- 1.60 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. I (1S,2S)-N-(6-(7-((S)-1-(1H-tetrazol-1- yl)ethyl)-5-chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 415 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40-13.49 (1H), 11.06-11.17 (1H), 8.83-8.91 (1H), 8.15-8.21 (1H), 8.02-8.09 (1H), 7.57-7.64 (1H), 7.38-7.46 (1H), 5.72-5.82 (1H), 4.82-5.07 (1H), 3.46-3.55 (3H), 2.12-2.21 (1H), 1.61-1.74 (1H), 1.13-1.22 (1H); LCMS (electrospray) m/z 501.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2,2,2- trifluoro-1-methoxyethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 416 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.23 (s, 1H), 11.06 (s, 1H), 8.72 (s, 1H), 8.16 (s, 1H), 7.88 (d, J = 1.1 Hz, 1H), 7.54 (d, J = 9.3 Hz, 1H), 7.32 (dd, J = 9.3, 1.6 Hz, 1H), 5.60-5.58 (m, 1H), 5.04-4.83 (m, 1H), 4.55 (s, 1H), 3.95 (q, J = 7.7 Hz, 1H), 3.87 (dd, J = 9.1, 5.8 Hz, 1H), 3.79-3.71 (m, 2H), 2.27- 2.13 (m, 2H), 1.91 (s, 1H), 1.67 (dtd, J = 23.5, 6.9, 3.7 Hz, 1H), 1.22-1.13 (m, 1H); LCMS (electrospray) m/z 474.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- ((tetrahydrofuran-3-yl)amino)-1H-indazol- 4-yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 417 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67-13.49 (m, 1H), 11.10 (s, 1H), 8.79 (s, 1H), 8.52 (d, J = 6.8 Hz, 1H), 8.16 (s, 1H), 7.98 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 1.6, 9.3 Hz, 1H), 5.45 (quin, J = 7.1 Hz, 1H), 5.07-4.81 (m, 1H), 2.22- 2.11 (m, 1H), 1.85 (s, 3H), 1.73-1.61 (m, 1H), 1.55 (d, J = 7.3 Hz, 3H), 1.17 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 473.2 (M + H)+. H (1S,2S)-N-(6-(7-(1-acetamidoethyl)-5- chloro-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 418 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 11.10 (s, 1H), 8.87 (s, 1H), 8.16-8.04 (m, 2H), 7.59 (d, J = 8.8 Hz, 1H), 7.41 (dd, J = 9.1, 1.9 Hz, 1H), 5.81 (q, J = 7.1 Hz, 1H), 5.04-4.83 (m, 1H), 3.79- 3.58 (m, 2H), 2.20-2.13 (m, 1H), 1.67 (dtd, J = 23.4, 6.8, 3.6 Hz, 1H), 1.23 (t, J = 7.1 Hz, 3H), 1.19-1.13 (m, 1H); LCMS (electrospray) m/z 514.7 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1-ethoxy-2,2,2- trifluoroethyl)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 419 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.78 (s, 1H), 11.12 (s, 1H), 8.89 (t, J = 1.4 Hz, 1H), 8.18 (s, 1H), 8.12 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.42 (dd, J = 9.1, 1.9 Hz, 1H), 7.06 (dt, J = 41.2, 6.7 Hz, 1H), 5.05-4.84 (m, 1H), 2.21-2.14 (m, 1H), 1.68 (dtd, J = 23.5, 6.9, 3.5 Hz, 1H), 1.24-1.14 (m, 1H); LCMS (electrospray) m/z 488.7 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- (1,2,2,2-tetrafluoroethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 420 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30 (br s, 1H), 11.05 (s, 1H), 8.72 (s, 1H), 8.14 (s, 1H), 7.87 (br s, 1H), 7.52 (d, J = 9.2 Hz, 1H), 7.31 (dd, J = 1.5, 9.2 Hz, 1H), 5.34 (br s, 1H), 5.04-4.82 (m, 1H), 2.16 (td, J = 7.0, 13.9 Hz, 1H), 1.73-1.61 (m, 1H), 1.26 (d, J = 6.3 Hz, 3H), 1.16 (ddd, J = 2.8, 6.2, 12.1 Hz, 1H), 1.00 (br s, 1H), 0.46-0.37 (m, 2H), 0.30- 0.20 (m, 2H); LCMS (electrospray) m/z 471.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((1- cyclopropylethyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 421 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.22 (br s, 1H), 11.06 (s, 1H), 8.71 (s, 1H), 8.14 (s, 1H), 7.86 (s, 1H), 7.52 (d, J = 9.1 Hz, 1H), 7.30 (d, J = 9.3 Hz, 1H), 5.57 (m, 1H), 4.92 (m, 1H), 3.30 (s, 2H), 2.15 (m, 1H), 1.66 (m, 1H), 1.16 (m, 1H), 1.07 (m, 1H), 0.48 (m, 2H), 0.27 (m, 2H); LCMS (electrospray) m/z 457.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- ((cyclopropylmethyl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 422 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52-13.66 (m, 1H), 11.09 (s, 1H), 8.80 (s, 1H), 8.16 (s, 1H), 7.97 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.36 (dd, J = 1.6 Hz, 1.6 Hz, 1H), 5.04-4.83 (m, 1H), 3.82- 3.74 (m, 3H), 3.68 (s, 1H), 2.20-2.14 (m, 1H), 1.71-1.63 (m, 1H), 1.22 (d, J = 7.4 Hz, 3H), 1.2- 1.14(m, 2H); LCMS (electrospray) m/z 460.0 (M + H)+; SFC RT = 0.640. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((R)-1- methoxypropan-2-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 423 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.57 (s, 1H), 11.09 (s, 1H), 8.80 (s, 1H), 8.16 (s, 1H), 7.98 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.35 (d, J = 1.6 Hz, 1H), 5.04-4.83 (m, 1H), 3.82-3.74 (m, 3H), 2.20-2.14 (m, 1H), 1.41-1.39 (m, 1H), 1.22 (d, J = 14.4 Hz, 3H), 1.2-1.17(m, 2H); LCMS (electrospray) m/z 460.0 (M + H)+; SFC RT = 1.252. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-((S)-1- methoxypropan-2-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 424 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64-13.32 (m, 1H), 11.09 (s, 1H), 8.79 (s, 1H), 8.32 (br d, J = 6.3 Hz, 1H), 8.16 (s, 1H), 7.98 (s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 1.7, 9.2 Hz, 1H), 5.46 (br t, J = 7.0 Hz, 1H), 5.05-4.81 (m, 1H), 2.19-2.07 (m, 3H), 1.74-1.60 (m, 1H), 1.55 (d, J = 7.3 Hz, 3H), 1.24-1.11 (m, 1H), 0.95 (t, J = 7.6 Hz, 3H); LCMS (electrospray) m/z 487.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- propionamidoethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 425 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55-13.09 (m, 1H), 11.07 (s, 1H), 8.73 (s, 1H), 8.16 (s, 1H), 8.07- 7.83 (m, 1H), 7.54 (d, J = 9.1 Hz, 1H), 7.32 (dd, J = 1.7, 9.1 Hz, 1H), 6.30-5.95 (m, 1H), 5.65-5.44 (m, 1H), 5.11-4.76 (m, 1H), 4.54-3.95 (m, 1H), 2.20-2.12 (m, 1H), 1.75-1.59 (m, 1H), 1.33 (d, J = 6.7 Hz, 3H), 1.17 (ddt J = 6.2, 6.2, 9.1, 12.2 Hz, 1H); LCMS (electrospray) m/z 481.0 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((1,1- difluoropropan-2-yl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 426 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.66-13.47 (m, 1H), 11.09 (s, 1H), 8.80 (s, 1H), 8.67 (br d, J = 6.8 Hz, 1H), 8.16 (s, 1H), 8.06 (s, 1H), 8.00 (br s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 1.4, 9.3 Hz, 1H), 5.62-5.48 (m, 1H), 5.09-4.80 (m, 1H), 2.16 (quin, J = 6.9 Hz, 1H), 1.73-1.61 (m, 1H), 1.57 (d, J = 7.0 Hz, 3H), 1.22-1.10 (m, 1H); LCMS (electrospray) m/z 458.9 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- formamidoethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 427 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.74-13.07 (m, 1H), 11.09 (s, 1H), 8.80 (s, 1H), 8.43 (s, 1H), 8.16 (s, 1H), 7.96 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.35 (dd, J = 1.7, 9.2 Hz, 1H), 5.06-4.80 (m, 1H), 4.60 (t, J = 6.4 Hz, 1H), 4.50-4.39 (m, 2H), 4.32 (t, J = 6.5 Hz, 1H), 4.15 (t, J = 6.2 Hz, 1H), 3.75 (br t, J = 6.7 Hz, 1H), 2.22-2.11 (m, 1H), 1.73- 1.60 (m, 1H), 1.49 (d, J = 6.7 Hz, 3H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 487.3 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (oxetan-3-ylamino)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 428 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30 (br s, 1H), 11.19 (s, 1H), 10.04 (d, J = 4.5 Hz, 1H), 8.84 (s, 1H), 8.16 (s, 1H), 8.04 (s, 1H), 7.62 (d, J = 9.1 Hz, 1H), 7.49-7.39 (m, 1H), 5.70-5.46 (m, 1H), 5.11- 4.78 (m, 1H), 2.17 (td, J = 6.9, 13.8 Hz, 1H), 1.69 (d, J = 7.0 Hz, 3H), 1.67-1.59 (m, 1H), 1.29-1.09 (m, 1H); LCMS (electrospray) m/z 527.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (2,2,2-trifluoroacetamido)ethyl)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 429 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30 (br s, 1H), 11.05 (s, 1H), 8.72 (s, 1H), 8.14 (s, 1H), 7.91 (s, 1H), 7.58 (d, J = 9.0 Hz, 1H), 7.38-7.32 (m, 1H), 5.09-4.81 (m, 1H), 4.08-3.99 (m, 1H), 2.19-2.13 (m, 1H), 1.71-1.62 (m, 1H), 1.51 (d, J = 6.7 Hz, 3H), 1.32-1.23 (m, 1H), 1.21-1.13 (m, 1H), 1.04- 0.94 (m, 1H), 0.69-0.56 (m, 1H); LCMS (electrospray) m/z 496.3 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1-((1- cyanocyclopropyl)amino)ethyl)-6-fluoro- 1H-indazol-4-yl)imidazo[1,2-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 430 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.99-13.36 (m, 1H), 11.09 (s, 1H), 8.79 (s, 1H), 8.51-8.44 (m, 1H), 8.46 (s, 1H), 8.41 (br d, J = 6.7 Hz, 1H), 8.15 (s, 1H), 7.97 (s, 1H), 7.57 (d, J = 9.2 Hz, 1H), 7.35 (dd, J = 1.7, 9.3 Hz, 1H), 5.45 (br t, J = 7.0 Hz, 1H), 5.07-4.76 (m, 1H), 3.14-3.03 (m, 1H), 2.10 (br d, J = 8.7 Hz, 1H), 2.21-2.01 (m, 1H), 2.00-1.81 (m, 4H), 1.64 (dt, J = 4.2, 6.7 Hz, 1H), 1.75-1.60 (m, 1H), 1.55 (br d, J = 7.2 Hz, 3H), 1.17 (ddd, J = 2.8, 6.2, 12.3 Hz, 1H); LCMS (electrospray) m/z 513.3 (M + H)+. H N-(1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)imidazo[1,2-a]pyridin-6-yl)- 1H-indazol-7- yl)ethyl)cyclobutanecarboxamide 431 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.37 (br s, 1H), 11.25 (s, 1H), 8.92 (s, 1H), 8.81 (d, J = 5.7 Hz, 1H), 8.22 (s, 1H), 8.19 (s, 1H), 8.10 (s, 1H), 7.66 (d, J = 9.2 Hz, 1H), 7.49 (d, J = 9.4 Hz, 1H), 5.06-4.89 (m, 1H), 2.24-2.15 (m, 1H), 1.78-1.62 (m, 1H), 1.26-1.17 (m, 1H), 0.30-0.20 (m, 2H); LCMS (electrospray) m/z 453.9 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1H- imidazol-5-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 432 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (s, 1H), 11.08 (s, 1H), 8.68 (s, 1H), 8.19 (s, 1H), 7.81 (s, 1H), 7.54 (d, J = 9.3 Hz, 1H), 7.30 (dd, J = 9.3, 1.6 Hz, 1H), 6.48 (d, J = 18.1 Hz, 2H), 4.93 (ddd, J = 66.4, 10.0, 6.2 Hz, 1H), 3.40 (s, 4H), 2.19-2.12 (m, 1H), 1.71-1.62 (m, 1H), 1.19-1.12 (m, 1H); LCMS (electrospray) m/z 472.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((4,5-dihydro- 1H-imidazol-2-yl)amino)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 433 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 1H-NMR (400 MHz, DMSO-D6) δ 13.31 (s, 1H), 11.11 (s, 1H), 8.79 (d, J = 1.6 Hz, 1H), 8.19 (s, 1H), 7.98 (d, J = 1.6 Hz, 1H), 7.94 (d, J = 4.9 Hz, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.35 (dd, J = 9.1, 1.9 Hz, 1H), 4.93 (ddd, J = 66.2, 10.2, 6.3 Hz, 1H), 4.25 (q, J = 7.1 Hz, 1H), 2.67-2.60 (m, 3H), 2.19-2.08 (m, 1H), 1.71-1.61 (m, 1H), 1.55 (d, J = 7.1 Hz, 3H), 1.24- 1.10 (m, 1H); LCMS (electrospray) m/z 473.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (methylamino)-1-oxopropan-2-yl)-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 434 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70 (s, 1H), 11.13 (s, 1H), 8.85 (s, 1H), 8.18 (s, 1H), 8.04-8.01 (m, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 9.3, 1.6 Hz, 1H), 5.05-4.84 (m, 1H), 4.10 (d, J = 12.6 Hz, 2H), 2.20-2.13 (m, 1H), 2.08 (d, J = 9.3 Hz, 3H), 1.67 (dtd, J = 23.3, 6.8, 3.7 Hz, 1H), 1.24-1.14 (m, 1H), LCMS (electrospray) m/z 449.05 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- ((methylthio)methyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 435 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.71 (s, 1H), 11.12 (s, 1H), 8.79 (s, 1H), 8.23 (s, 1H), 8.03 (d, J = 1.1 Hz, 1H), 7.60 (d, J = 9.3 Hz, 1H), 7.36 (dd, J = 9.3, 1.6 Hz, 1H), 6.42 (s, 1H), 5.04-4.84 (m, 1H), 3.21 (s, 3H), 2.58 (d, J = 4.4 Hz, 3H), 2.20-2.13 (m, 1H), 1.70-1.63 (m, 1H), 1.19-1.13 (m, 1H) m/z 474.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1,3- dimethylureido)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 436 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.58 (s, 1H), 11.12 (s, 1H), 8.82 (t, J = 1.4 Hz, 1H), 8.18 (d, J = 12.1 Hz, 1H), 8.01 (s, 1H), 7.58 (d, J = 9.3 Hz, 1H), 7.38 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 1H), 4.64 (q, J = 7.1 Hz, 1H), 2.19-2.12 (m, 1H), 2.02- 1.96 (m, 3H), 1.81-1.77 (m, 3H), 1.66 (dtd, J = 23.3, 6.9, 3.8 Hz, 1H), 1.21-1.13 (m, 1H), LCMS (electrospray) m/z 463.00 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (methylthio)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 437 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.71 (s, 1H), 11.12 (s, 1H), 8.85 (d, J = 1.1 Hz, 1H), 8.21-8.16 (m, 1H), 8.03 (d, J = 1.1 Hz, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 1H), 4.54-4.43 (m, 2H), 2.68 (d, J = 13.7 Hz, 3H), 2.20-2.13 (m, 1H), 1.67 (dtd, J = 23.3, 6.9, 3.8 Hz, 1H), 1.20-1.13 (m, 1H) LCMS (electrospray) m/z 465.00 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- ((methylsulfinyl)methyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 438 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69 (s, 1H), 11.12 (s, 1H), 8.85 (t, J = 1.4 Hz, 1H), 8.18 (s, 1H), 8.04 (s, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 3H), 3.11 (s, 3H), 2.19-2.12 (m, 1H), 1.66 (dtd, J = 23.5, 6.7, 3.5 Hz, 1H), 1.22-1.13 (m, 1H), LCMS (electrospray) m/z 481.00 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7- ((methylsulfonyl)methyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 439 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.81 (s, 1H), 11.14 (s, 1H), 9.65 (d, J = 6.0 Hz, 1H), 8.86 (s, 1H), 8.21 (d, J = 8.8 Hz, 2H), 8.13 (s, 1H), 7.61 (d, J = 9.3 Hz, 1H), 7.39 (dd, J = 9.1, 1.4 Hz, 1H), 6.69 (d, J = 6.6 Hz, 1H), 5.05-4.84 (m, 1H), 2.21-2.14 (m, 1H), 1.73-1.62 (m, 1H), 1.22-1.14 (m, 1H), LCMS (electrospray) m/z 471.00 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7- (cyano(formamido)methyl)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 440 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.33 (s, 1H), 11.12 (s, 1H), 8.85 (t, J = 1.4 Hz, 1H), 8.16 (s, 1H), 7.97 (d, J = 0.8 Hz, 1H), 7.58 (d, J = 8.8 Hz, 1H), 7.39 (dd, J = 9.3, 1.6 Hz, 1H), 5.04-4.83 (m, 2H), 3.93-3.87 (m, 1H), 3.38 (d, J = 3.3 Hz, 2H), 3.24 (s, 3H), 2.16 (dt, J = 14.4, 6.7 Hz, 1H), 1.66 (dtd, J = 23.2, 6.9, 3.8 Hz, 1H), 1.24-1.13 (m, 1H), 0.95 (d, J = 6.0 Hz, 3H); LCMS (electrospray) m/z 490.10 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-((1S,2R)-1,2- dimethoxypropyl)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 441 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.60 (br s, 1H), 11.08 (s, 1H), 9.39 (br d, J = 6.5 Hz, 1H), 8.80 (s, 1H), 8.16 (s, 1H), 8.02 (br s, 1H), 7.57 (d, J = 9.3 Hz, 1H), 7.36 (dd, J = 1.8, 9.2 Hz, 1H), 6.28 (t, J = 53.6 Hz, 1H), 5.55 (br t, J = 6.8 Hz, 1H), 5.04- 4.81 (m, 1H), 2.23-2.10 (m, 1H), 1.73-1.67 (m, 1H), 1.65 (d, J = 7.2 Hz, 3H), 1.17 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 509.2 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1-(2,2- difluoroacetamido)ethyl)-6-fluoro-1H- indazol-4-yl)imidazo[1,2-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 442 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.20 (s, 1H), 12.37 (d, J = 1.3 Hz, 1H), 11.08 (s, 1H), 8.85 (s, 1H), 8.18 (s, 1H), 8.00 (s, 1H), 7.67 (d, J = 3.1 Hz, 1H), 7.58 (d, J = 9.2 Hz, 1H), 7.40 (dd, J = 1.7. 9.2 Hz, 1H), 4.93 (m, 1H), 2.48 (s, 3H), 2.16 (m, 2H), 1.67 (m, 2H), 1.17 (m, 2H); LCMS (electrospray) m/z 468.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(2- methyl-1H-imidazol-5-yl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 443 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68 (s, 1H), 11.11 (s, 1H), 8.81 (d, J = 1.1 Hz, 1H), 8.17 (d, J = 9.3 Hz, 1H), 8.05 (d, J = 1.1 Hz, 1H), 7.59 (d, J = 9.3 Hz, 1H), 7.37 (dd, J = 9.1, 1.9 Hz, 1H), 5.04- 4.83 (m, 1H), 4.64-4.59 (m, 1H), 2.48 (s, 2H), 2.19-2.12 (m, 1H), 1.83-1.81 (m, 3H), 1.71-1.61 (m, 1H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 478.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (methylsulflnyl)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 444 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.54 (s, 1H), 11.12 (s, 1H), 8.84 (s, 1H), 8.18 (s, 1H), 8.04 (s, 1H), 7.60 (d, J = 9.3 Hz, 1H), 7.38 (dd, J = 9.3, 1.6 Hz, 1H), 5.15 (d, J = 7.1 Hz, 1H), 5.04-4.83 (m, 1H), 3.06 (s, 3H), 2.20-2.13 (m, 1H), 1.97-1.91 (m, 3H), 1.72-1.62 (m, 1H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 494.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-6-fluoro-7-(1- (methylsulfonyl)ethyl)-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 445 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26 (s, 1H), 11.08 (s, 1H), 8.79 (s, 1H), 8.18 (s, 1H), 8.00 (d, J = 23.6 Hz, 2H), 7.58 (d, J = 8.8 Hz, 1H), 7.35 (dd, J = 9.1, 1.9 Hz, 1H), 5.04-4.83 (m, 1H), 4.24 (q, J = 7.1 Hz, 1H), 3.11 (td, J = 12.6, 7.1 Hz, 2H), 2.20- 2.13 (m, 1H), 1.70-1.63 (m, 1H), 1.54 (d, J = 7.1 Hz, 3H), 1.21-1.13 (m, 1H), 1.01 (t, J = 7.1 Hz, 3H); LCMS (electrospray) m/z 487.1 (M + H)+. H (1S,2S)-N-(6-(5-chloro-7-(1-(ethylamino)- 1-oxopropan-2-yl)-6-fluoro-1H-indazol-4- yl)imidazo[1,2-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 446 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.09 (s, 1H), 11.13 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.74 (s, 1H), 7.63 (d, J = 0.9 Hz, 1H), 7.49 (d, J = 8.6 Hz, 1H), 7.32 (d, J = 8.6 Hz, 1H), 6.91 (s, 1H), 6.86 (dd, J = 1.9, 7.0 Hz, 1H), 5.06-4.98 (m, 1H), 4.88-4.84 (m, 1H), 2.34 (s, 3H), 2.15 (td, J = 6.9, 13.8 Hz, 1H), 1.74- 1.61 (m, 1H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 350.1 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(5-methyl-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 447 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.82 (s, 1H), 7.65 (d, J = 0.9 Hz, 1H), 7.45 (d, J = 11.5 Hz, 1H), 6.93 (s, 1H), 6.81 (dd, J = 1.8, 7.1 Hz, 1H), 6.56 (dd, J = 11.8, 17.9 Hz, 1H), 5.63 (br d, J = 18.0 Hz, 1H), 5.46-5.36 (m, 1H), 5.06-4.82 (m, 1H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.73-1.59 (m, 1H), 1.17 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H)); LCMS (electrospray) m/z 380.1 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-vinyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 HCl 448 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.88 (d, J = 1.0 Hz, 1H), 7.75 (d, J = 1.0 Hz, 1H), 7.63 (dd, J = 1.0, 8.8 Hz, 1H), 7.51 (d, J = 8.8 Hz, 1H), 6.95 (s, 1H), 6.92 (dd, J = 2.0, 7.1 Hz, 1H), 5.05-4.83 (m, 1H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.17 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z 370.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl 449 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.10 (s, 1H), 8.56 (br d, J = 7.0 Hz, 1H), 7.90 (s, 1H), 7.74 (s, 1H), 7.58 (br d, J = 9.2 Hz, 1H), 7.35 (d, J = 8.9 Hz, 1H), 6.98 (br d, J = 7.1 Hz, 1H), 6.89 (s, 1H), 5.08- 4.80 (m, 1H), 3.80 (s, 3H), 2.19-2.08 (m, 1H), 1.75-1.60 (m, 1H), 1.26-1.07 (m, 1H); LCMS (electrospray) m/z 366.1 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(5-methoxy-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 HCl 450 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.18 (br s, 1H), 8.68 (br s, 1H), 8.12-7.54 (m, 5H), 7.04-6.85 (m, 2H), 5.05-4.84 (m, 1H), 3.10 (br s, 6H), 2.16 (td, J = 7.0, 14.0 Hz, 1H), 1.73-1.62 (m, 1H), 1.23-1.14 (m, 1H); LCMS (electrospray) m/z 379.1 (M + H)+. J (1S,2S)-N-(5-(5-(dimethylamino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 3 HCl 451 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.19-13.15 (m, 1H), 11.17 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.87 (s, 1H), 7.82-7.74 (m, 2H), 7.64 (s, 1H), 6.93 (s, 1H), 6.83 (dd, J = 1.8, 7.1 Hz, 1H), 5.08-4.81 (m, 1H), 2.20-2.10 (m, 1H), 1.74-1.59 (m, 1H), 1.17 (tdd, J = 6.2, 9.0, 12.4 Hz, 1H); LCMS (electrospray) m/z 404.1 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(5- (trifluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 HCl 452 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.10 (br s, 1H), 11.13 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.68 (s, 1H), 7.59 (d, J = 1.0 Hz, 1H), 7.53 (d, J = 8.6 Hz, 1H), 7.36 (d, J = 8.7 Hz, 1H), 6.90 (s, 1H), 6.81 (dd, J = 1.9, 7.0 Hz, 1H), 5.06-4.81 (m, 1H), 2.70-2.59 (m, 2H), 2.20-2.10 (m, 1H), 1.75-1.58 (m, 1H), 1.18 (td, J = 3.1, 6.1 Hz, 1H), 1.12 (t, J = 7.5 Hz, 3H); LCMS (electrospray) m/z 364.2 (M + H)+. J (1S,2S)-N-(5-(5-ethyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 453 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.97 (d, J = 0.7 Hz, 1H), 7.77 (d, J = 8.8 Hz, 1H), 7.69-7.64 (m, 1H), 7.61 (d, J = 1.1 Hz, 1H), 6.92 (s, 1H), 6.82 (dd, J = 2.0, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 2.33 (s, 3H), 2.21- 2.11 (m, 1H), 1.73-1.61 (m, 1H), 1.18 (tdd, J = 6.1, 8.9, 12.3 Hz, 1H); LCMS (electrospray) m/z 378.2 (M + H)+. J (1S,2S)-N-(5-(5-acetyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl 454 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.11 (s, 1H), 8.58 (d, J = 7.1 Hz, 1H), 7.82 (s, 1H), 7.66 (s, 1H), 7.40 (d, J = 12.0 Hz, 1H), 6.93-6.87 (m, 2H), 5.05- 4.82 (m, 1H), 2.67 (s, 6H), 2.19-2.09 (m, 1H), 1.73-1.61 (m, 1H), 1.22-1.12 (m, 1H); LCMS (electrospray) m/z = 397.1 (M + H+) J (1S,2S)-N-(5-(5-(dimethylamino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 3 TFA 455 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43 (br s, 1H), 11.15 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.83 (s, 1H), 7.70 (dd, J = 0.8, 1.8 Hz, 1H), 7.67-7.63 (m, 1H), 7.58-7.55 (m, 1H), 6.95 (s, 1H), 6.88 (dd, J = 1.9, 7.2 Hz, 1H), 5.05-4.83 (m, 1H), 2.20-2.10 (m, 1H), 1.72-1.61 (m, 1H), 1.18 (qd, J = 6.2, 15.1 Hz, 1H); LCMS (electrospray) m/z = 414.0 (M + H+) J (1S,2S)-N-(5-(5-bromo-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 456 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.21 (s, 1H), 8.73 (d, J = 7.2 Hz, 1H), 8.19 (s, 1H), 7.94 (d, J = 1.2 Hz, 1H), 7.85-7.73 (m, 2H), 7.09 (dd, J = 2.0, 7.1 Hz, 1H), 7.02 (s, 1H), 5.08-4.82 (m, 1H), 2.16 (td, J = 7.0, 13.8 Hz, 1H), 1.74-1.62 (m, 1H), 1.18 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS (electrospray): m/z = 361.1 (M + H+) J (1S,2S)-N-(5-(5-cyano-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 HCl 457 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.83 (s, 1H), 7.74 (d, J = 0.9 Hz, 1H), 7.34 (d, J = 10.5 Hz, 1H), 6.98 (dd, J = 1.8, 7.1 Hz, 1H), 6.92 (s, 1H), 5.06-4.99 (m, 1H), 4.90- 4.82 (m, 1H), 2.15 (td, J = 7.0, 13.6 Hz, 1H), 2.01- 1.93 (m, 1H), 1.74-1.61 (m, 1H), 1.22-1.13 (m, 1H), 0.77-0.69 (m, 2H), 0.33-0.25 (m, 2H); LCMS (electrospray) m/z = 394.1 (M + H+) J (1S,2S)-N-(5-(5-cyclopropyl-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 458 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.50 (br s, 1H), 11.17 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 7.92 (s, 1H), 7.79 (d, J = 1.0 Hz, 1H), 7.68 (dd, J = 0.9, 9.0 Hz, 1H), 6.97 (s, 1H), 6.96 (d, J = 2.0 Hz, 1H), 6.96- 6.93 (m, 1H), 5.06-5.00 (m, 1H), 4.88-4.84 (m, 1H), 2.18-2.12 (m, 1H), 1.75-1.59 (m, 1H), 1.22- 1.14 (tdd, J = 6.2, 9.2, 12.4 Hz, 1H); LCMS (electrospray)m/z = 388.0 (M + H+) J (1S,2S)-N-(5-(5-chloro-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 459 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.10 (s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.75-7.67 (m, 2H), 7.48 (d, J = 8.8 Hz, 1H), 7.02 (d, J = 8.8 Hz, 1H), 6.96-6.88 (m, 2H), 5.07-4.82 (m, 1H), 2.20- 2.08 (m, 1H), 2.03-1.94 (m, 1H), 1.74-1.60 (m, 1H), 1.22-1.11 (m, 1H), 0.90-0.78 (m, 2H), 0.70- 0.60 (m, 2H); LCMS (electrospray) m/z = 376.1 (M + H+) J (1S,2S)-N-(5-(5-cyclopropyl-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 460 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.17 (br s, 1H), 11.15 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.77 (s, 1H), 7.67 (d, J = 0.9 Hz, 1H), 7.38 (d, J = 9.9 Hz, 1H), 6.93 (s, 1H), 6.87 (dd, J = 2.0, 7.1 Hz, 1H), 5.06-4.81 (m, 1H), 2.23 (d, J = 2.6 Hz, 3H), 2.15 (td, J = 6.9, 13.8 Hz, 1H), 1.75-1.59 (m, 1H), 1.17 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z = 368.1 (M + H+) J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 461 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (br s, 1H), 11.14 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.82 (s, 1H), 7.69 (s, 1H), 7.58 (s, 2H), 6.94 (dd, J = 1.9, 7.0 Hz, 1H), 6.91 (s, 1H), 5.09-4.80 (m, 1H), 4.50 (s, 2H), 2.22-2.09 (m, 1H), 1.75-1.58 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z = 366.0 (M + H+) J (1S,2S)-2-fluoro-N-(5-(5- (hydroxymethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 462 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 8.63 (d, J = 7.0 Hz, 1H), 7.64 (d, J = 3.1 Hz, 1H), 7.59 (d, J = 0.8 Hz, 1H), 7.36 (d, J = 12.3 Hz, 1H), 6.92 (s, 1H), 6.78 (dd, J = 1.8, 7.1 Hz, 1H), 5.07-4.97 (m, 1H), 4.88-4.84 (m, 1H), 3.13-3.00 (m, 1H), 2.18- 2.11 (m, 1H), 1.74-1.60 (m, 1H), 1.28 (dd, J = 7.1, 11.6 Hz, 6H), 1.21-1.08 (m, 1H); LCMS (electrospray) m/z = 396.1 (M + H+) J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- isopropyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 463 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.25 (br s, 1H), 11.33-10.98 (m, 1H), 11.13 (s, 1H), 8.61 (d, J = 7.0 Hz, 1H), 7.76 (s, 1H), 7.66-7.59 (m, 2H), 7.56-7.51 (m, 1H), 6.92 (s, 1H), 6.87 (dd, J = 1.8, 7.1 Hz, 1H), 5.23-4.71 (m, 1H), 2.39 (s, 3H), 2.20-2.10 (m, 1H), 1.75-1.58 (m, 1H), 1.17 (tdd, J = 6.2, 9.1, 12.2 Hz, 1H); LCMS (electrospray) m/z = 382.1 (M + H+) J (1S,2S)-2-fluoro-N-(5-(5-(methylthio)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 464 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (br s, 1H), 11.17 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.86 (s, 1H), 7.74 (d, J = 1.0 Hz, 1H), 7.66-7.61 (m, 1H), 6.96 (s, 1H), 6.90 (dd, J = 2.0, 7.1 Hz, 1H), 5.08-4.80 (m, 1H), 2.14 (br d, J = 7.2 Hz, 1H), 1.75-1.60 (m, 1H), 1.21-1.14 (m, 1H); LCMS (electrospray) m/z = 432.0 (M + H+) J (1S,2S)-N-(5-(5-bromo-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 465 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52 (br s, 1H), 11.17 (s, 1H), 8.67 (d, J = 7.0 Hz, 1H), 7.94 (s, 1H), 7.78-7.74 (m, 1H), 7.73-7.69 (m, 1H), 7.66 (s, 1H), 7.11-6.80 (m, 3H), 5.07-4.83 (m, 1H), 2.19- 2.10 (m, 1H), 1.74-1.62 (m, 1H), 1.18 (tdd, J = 6.4, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z = 386.2 (M + H+) J (1S,2S)-N-(5-(5-(difluoromethyl)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 466 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.15 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.70 (s, 1H), 7.63 (s, 1H), 7.39 (d, J = 10.4 Hz, 1H), 6.93 (s, 1H), 6.82 (dd, J = 1.8, 7.0 Hz, 1H), 5.06-4.81 (m, 1H), 2.66-2.57 (m, 2H), 2.20-2.09 (m, 1H), 1.74-1.60 (m, 1H), 1.22-1.14 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS (electrospray) m/z = 382.1 (M + H+) J (1S,2S)-N-(5-(5-ethyl-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 467 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27 (s, 1H), 11.15 (s, 1H), 8.67-8.61 (m, 1H), 7.97 (s, 1H), 7.84-7.80 (m, 1H), 7.56-7.48 (m, 1H), 7.05-6.99 (m, 1H), 6.95 (s, 1H), 5.08-4.82 (m, 1H), 3.67 (s, 2H), 3.71-3.63 (m, 1H), 2.07 (s, 1H), 1.75-1.61 (m, 1H), 1.26-1.09 (m, 1H); LCMS (electrospray) m/z = 384.1 (M + H+) J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- methoxy-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 468 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.60 (br s, 1H), 11.21 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.93 (s, 1H), 7.69 (s, 1H), 7.60 (d, J = 11.2 Hz, 1H), 7.09-6.79 (m, 3H), 5.08-4.81 (m, 1H), 2.19-2.11 (m, 1H), 1.73-1.61 (m, 1H), 1.23-1.14 (m, 1H); LCMS (electrospray) m/z = 404.1 (M + H+) J (1S,2S)-N-(5-(5-(difluoromethyl)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 469 05embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (s, 1H), 11.14 (br d, J = 3.1 Hz, 1H), 8.62 (d, J = 7.0 Hz, 1H), 7.52 (s, 1H), 7.44 (d, J = 9.8 Hz, 1H), 6.90 (s, 1H), 6.74 (dd, J = 1.8, 7.1 Hz, 1H), 5.09-4.79 (m, 1H), 2.19-2.12 (m, 1H), 2.09 (t, J = 2.4 Hz, 3H), 1.75- 1.60 (m, 1H), 1.23-1.09 (m, 1H); LCMS (electrospray) m/z = 402.0 (M + H+) J (1S,2S)-N-(5-(3-chloro-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 470 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (d, J = 3.5 Hz, 1H), 8.63 (d, J = 7.0 Hz, 1H), 7.53 (d, J = 0.7 Hz, 1H), 7.29 (d, J = 10.0 Hz, 1H), 6.91 (s, 1H), 6.75 (dd, J = 1.8, 7.0 Hz, 1H), 5.11-4.79 (m, 1H), 2.15 (td, J = 6.8, 13.4 Hz, 1H), 2.07 (t, J = 2.4 Hz, 3H), 1.90 (d, J = 4.3 Hz, 3H), 1.74-1.59 (m, 1H), 1.24- 1.10 (m, 1H); LCMS (electrospray) m/z 382.0 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-3,5- dimethyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA s 471 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.37 (s, 1H), 11.15 (s, 1H), 8.59 (d, J = 7.1 Hz, 1H), 7.60 (d, J = 1.0 Hz, 1H), 6.95 (d, J = 10.1 Hz, 1H), 6.91 (s, 1H), 6.88 (dd, J = 2.0, 7.1 Hz, 1H), 5.11-4.77 (m, 1H), 2.43 (s, 6H), 2.14 (td, J = 6.9, 13.9 Hz, 1H), 1.74-1.60 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 414.4 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 3-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 472 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53 (s, 1H), 11.15 (br d, J = 5.6 Hz, 1H), 8.59 (d, J = 7.0 Hz, 1H), 7.52 (s, 1H), 7.45 (d, J = 9.7 Hz, 1H), 6.90 (s, 1H), 6.75 (dd, J = 1.7, 7.0 Hz, 1H), 5.09-4.80 (m, 1H), 3.79 (d, J = 2.9 Hz, 1H), 2.20-2.14 (m, 1H), 2.12 (br d, J = 1.7 Hz, 3H), 1.74-1.59 (m, 1H), 1.27- 1.08 (m, 1H); LCMS (electrospray) m/z 392.2 (M + H+) J (1S,2S)-N-(5-(3-ethynyl-6-fluoro-5- methyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 473 09embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.49 (d, J = 7.2 Hz, 1H), 7.51 (s, 1H), 7.17 (d, J = 9.7 Hz, 1H), 6.80 (br d, J = 5.4 Hz, 1H), 4.98-4.76 (m, 1H), 2.15 (s, 3H), 2.12-2.03 (m, 1H), 1.87-1.73 (m, 1H), 1.40-1.30 (m, 1H), 1.27-1.15 (m, 1H), 0.83-0.74 (m, 1H), 0.69 (br s, 1H), 0.55-0.40 (m, 2H); LCMS (electrospray) m/z 408.4 (M + H+) J (1S,2S)-N-(5-(3-cyclopropyl-6-fluoro-5- methyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 474 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.17 (d, J = 4.4 Hz, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.53 (s, 1H), 7.37 (d, J = 9.8 Hz, 1H), 6.91 (s, 1H), 6.73 (dd, J = 1.8, 7.1 Hz, 1H), 6.04-5.92 (m, 1H), 5.85-5.75 (m, 1H), 5.06-4.82 (m, 2H), 2.15 (br d, J = 6.5 Hz, 1H), 2.07 (t, J = 2.4 Hz, 3H), 1.74-1.60 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 394.3 (M + H+) J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 3-vinyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 475 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (br d, J = 4.8 Hz, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.55 (s, 1H), 7.29 (d, J = 9.9 Hz, 1H), 6.90 (s, 1H), 6.76 (dd, J = 1.8, 7.0 Hz, 1H), 5.07-4.81 (m, 1H), 2.31-2.24 (m, 2H), 2.14 (br d, J = 6.7 Hz, 1H), 2.06 (t, J = 2.4 Hz, 3H), 1.75-1.59 (m, 1H), 1.24-1.09 (m, 1H), 0.90 (dt, J = 4.0, 7.5 Hz, 3H); LCMS (electrospray) m/z 396.3 (M + H+) J (1S,2S)-N-(5-(3-ethyl-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 476 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.12 (br d, J = 0.7 Hz, 1H), 11.18 (s, 1H), 8.69 (d, J = 7.2 Hz, 1H), 8.04 (br s, 1H), 7.80 (s, 1H), 6.98 (s, 1H), 6.95 (dd, J = 1.8, 7.1 Hz, 1H), 5.05-4.84 (m, 1H), 2.18- 2.11 (m, 1H), 1.73-1.62 (m, 1H), 1.23-1.15 (m, 1H); LCMS (electrospray) m/z 422.1 (M + H)+. J (1S,2S)-N-(5-(5,7-dichloro-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 477 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31 (br s, 1H), 11.14 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.77 (s, 1H), 7.63 (d, J = 1.0 Hz, 1H), 6.92 (s, 1H), 6.84 (dd, J = 1.8, 7.1 Hz, 1H), 5.11-4.75 (m, 1H), 2.47 (d, J = 1.6 Hz, 3H), 2.22 (d, J = 2.9 Hz, 3H), 2.15 (td, J = 6.8, 13.8 Hz, 1H), 1.74-1.60 (m, 1H), 1.17 (tdd, J = 6.3, 9.1, 12.4 Hz, 1H); LCMS (electrospray) m/z 382.4 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5,7- dimethyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 478 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16-12.54 (m, 1H), 11.20 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.00 (s, 1H), 7.82 (s, 1H), 7.00 (s, 1H), 6.96 (dd, J = 1.8, 7.2 Hz, 1H), 5.11-4.79 (m, 1H), 2.15 (td, J = 6.9, 13.8 Hz, 1H), 1.96 (s, 3H), 1.92 (s, 3H), 1.76-1.60 (m, 1H), 1.18 (tdd, J = 6.4, 9.1, 12.2 Hz, 1H); LCMS (electrospray) m/z 464.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- (dimethylphosphoryl)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 479 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.80 (br s, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.90 (br s, 1H), 7.69 (s, 1H), 6.94 (s, 1H), 6.87 (dd, J = 2.0, 7.1 Hz, 1H), 5.10-4.78 (m, 1H), 2.27 (d, J = 2.8 Hz, 3H), 2.19-2.07 (m, 1H), 1.74-1.60 (m, 1H), 1.24- 1.11 (m, 1H); LCMS (electrospray) m/z 402.0 (M + H)+. J (1S,2S)-N-(5-(7-chloro-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 480 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.00 (br s, 1H), 11.18 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 8.08 (br s, 1H), 7.80 (d, J = 0.8 Hz, 1H), 6.98 (s, 1H), 6.95 (dd, J = 1.9, 7.2 Hz, 1H), 5.08-4.79 (m, 1H), 2.15 (td, J = 7.0, 13.6 Hz, 1H), 1.75-1.60 (m, 1H), 1.26- 1.09 (m, 1H); LCMS (electrospray) m/z 466.3 (M + H)+. J (1S,2S)-N-(5-(7-bromo-5-chloro-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 481 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.54 (d, J = 7.1 Hz, 1H), 7.85 (d, J = 3.2 Hz, 1H), 7.59 (s, 1H), 6.98 (s, 1H), 6.86 (dd, J = 1.9, 7.2 Hz, 1H), 5.00- 4.96 (m, 1H), 2.34 (d, J = 3.2 Hz, 3H), 2.20-2.16 (m, 1H), 1.92-1.72 (m, 1H), 1.30-1.15 (m, 1H); LCMS (electrospray) m/z 386.0 (M + H)+. J (1S,2S)-N-(5-(6,7-difluoro-5-methyl-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 482 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.55 (d, J = 7.1 Hz, 1H), 7.89 (s, 1H), 7.63 (s, 1H), 7.00 (s, 1H), 6.87 (dd, J = 1.7, 7.1 Hz, 1H), 4.99-4.91 (m, 1H), 2.31 (d, J = 3.1 Hz, 3H), 2.14-2.04 (m, 1H), 1.87-1.75 (m, 1H), 1.27-1.16 (m, 1H); LCMS (electrospray) m/z 435.9 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(trifluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 483 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.36 (br s, 1H), 11.16 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.81 (s, 1H), 7.65 (s, 1H), 7.52 (s, 1H), 7.15 (dd, J = 11.1, 18.0 Hz, 1H), 6.92 (s, 1H), 6.87 (dd, J = 1.8, 7.1 Hz, 1H), 6.11 (br d, J = 17.6 Hz, 1H), 5.51 (d, J = 11.6 Hz, 1H), 5.05-4.85 (m, 1H), 2.36 (s, 3H), 2.14 (br d, J = 8.1 Hz, 1H), 1.72-1.64 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 376.1 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(5-methyl-7-vinyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 484 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (br s, 1H), 11.16 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.87 (s, 1H), 7.73 (d, J = 1.0 Hz, 1H), 6.95 (s, 1H), 6.91 (dd, J = 1.9, 7.2 Hz, 1H), 5.10-4.78 (m, 1H), 3.00 (br s, 6H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.74-1.61 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 431.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 485 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.79 (s, 1H), 11.17 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.98 (s, 1H), 7.79 (d, J = 1.0 Hz, 1H), 6.98 (s, 1H), 6.94 (dd, J = 2.0, 7.1 Hz, 1H), 5.08-4.77 (m, 1H), 2.57 (s, 3H), 2.15 (td, J = 6.9, 13.9 Hz, 1H), 1.74-1.61 (m, 1H), 1.18 (tdd, J = 6.3, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 434.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 486 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (br s, 1H), 11.20 (s, 1H), 8.72 (d, J = 7.2 Hz, 1H), 8.10 (s, 1H), 7.84 (d, J = 1.0 Hz, 1H), 7.02 (s, 1H), 6.96 (dd, J = 1.9, 7.2 Hz, 1H), 5.07-4.77 (m, 1H), 3.56 (s, 3H), 2.15 (quin, J = 6.9 Hz, 1H), 1.75-1.58 (m, 1H), 1.18 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z 466.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylsulfonyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 487 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69 (br s, 1H), 11.19 (s, 1H), 8.66 (d, J = 7.0 Hz, 1H), 7.92 (br s, 1H), 7.69 (d, J = 1.0 Hz, 1H), 6.94 (s, 1H), 6.87 (dd, J = 1.9, 7.1 Hz, 1H), 5.07-4.82 (m, 1H), 2.27 (d, J = 3.0 Hz, 3H), 2.20-2.10 (m, 1H), 1.74-1.60 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 448.1 (M + H)+. J (1S,2S)-N-(5-(7-bromo-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 488 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (s, 1H), 11.18 (s, 1H), 8.65 (d, J = 7.0 Hz, 1H), 7.84 (s, 1H), 7.68 (s, 1H), 6.93 (s, 1H), 6.87 (dd, J = 1.9, 7.1 Hz, 1H), 5.05-4.84 (m, 1H), 2.52 (br s, 3H), 2.24 (d, J = 2.9 Hz, 3H), 2.19-2.10 (m, 1H), 1.73-1.61 (m, 1H), 1.22-1.13 (m, 1H); LCMS (electrospray) m/z 414.2 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 489 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.23 (s, 1H), 11.21 (s, 1H), 8.70 (d, J = 7.2 Hz, 1H), 7.95 (s, 1H), 7.74 (d, J = 0.9 Hz, 1H), 6.97 (s, 1H), 6.90 (dd, J = 1.9, 7.2 Hz, 1H), 5.05-4.84 (m, 1H), 3.50 (s, 3H), 2.27 (d, J = 2.8 Hz, 3H), 2.15 (td, J = 6.9, 13.9 Hz, 1H), 1.73-1.62 (m, 1H), 1.25-1.12 (m, 1H); LCMS (electrospray) m/z 446.2 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylsulfonyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 490 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 8.62 (d, J = 7.2 Hz, 1H), 7.75 (s, 1H), 7.61 (d, J = 1.0 Hz, 1H), 6.90 (s, 1H), 6.84 (dd, J = 1.9, 7.1 Hz, 1H), 5.05-5.00 (m, 1H), 4.88-4.83 (m, 1H), 2.96 (d, J = 2.0 Hz, 6H), 2.20 (d, J = 3.4 Hz, 3H), 2.17- 2.09 (m, 1H), 1.73-1.61 (m, 1H), 1.21-1.12 (m, 1H); LCMS (electrospray) m/z 411.2 (M + H)+. J (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-methyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 491 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.14 (s, 1H), 8.62 (d, J = 7.0 Hz, 1H), 7.79 (br s, 1H), 7.62 (d, J = 1.0 Hz, 1H), 6.91 (s, 1H), 6.84 (dd, J = 1.9, 7.1 Hz, 1H), 5.08-4.80 (m, 1H), 4.08 (s, 3H), 2.23 (d, J = 3.1 Hz, 3H), 2.15 (td, J = 6.9, 14.0 Hz, 1H), 1.75-1.59 (m, 1H), 1.24-1.11 (m, 1H); LCMS (electrospray) m/z 398.2 (M + H)+. J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7- methoxy-5-methyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 492 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.84 (br s, 1H), 11.16 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.94 (s, 1H), 7.77-7.72 (m, 1H), 6.96 (s, 1H), 6.91 (dd, J = 1.9, 7.1 Hz, 1H), 5.09-4.77 (m, 1H), 4.16 (d, J = 1.5 Hz, 3H), 2.15 (td, J = 6.9, 13.7 Hz, 1H), 1.74-1.59 (m, 1H), 1.24-1.10 (m, 1H); LCMS (electrospray) m/z 418.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- methoxy-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 493 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.80 (br s, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.94 (br s, 1H), 7.75 (s, 1H), 6.95 (s, 1H), 6.92 (dd, J = 1.8, 7.2 Hz, 1H), 5.13-4.78 (m, 1H), 4.39 (br d, J = 6.5 Hz, 2H), 2.21-2.09 (m, 1H), 1.74-1.60 (m, 1H), 1.41 (t, J = 7.0 Hz, 3H), 1.24-1.12 (m, 1H); LCMS (electrospray) m/z 432.4 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-ethoxy-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 494 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.14 (s, 1H), 8.60 (d, J = 7.1 Hz, 1H), 7.88 (s, 1H), 7.68 (dd, J = 0.8, 1.8 Hz, 1H), 6.92 (s, 1H), 6.89 (dd, J = 2.0, 7.1 Hz, 1H), 5.08-4.78 (m, 1H), 3.17 (d, J = 2.8 Hz, 3H), 2.14 (td, J = 7.0, 13.9 Hz, 1H), 1.74-1.58 (m, 1H), 1.17 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z 417.4 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylamino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 495 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br d, J = 2.8 Hz, 1H), 11.18 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 8.17 (s, 1H), 7.90 (br s, 1H), 7.77-7.68 (m, 1H), 6.95 (s, 1H), 6.91 (dd, J = 2.0, 7.1 Hz, 1H), 5.06- 4.83 (m, 1H), 3.30 (br s, 4H), 2.57 (br s, 4H), 2.28 (s, 3H), 2.19-2.10 (m, 1H), 1.73-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS (electrospray) m/z 486.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(4- methylpiperazin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 FA 496 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (1 H, s) 8.62 (1 H, d, J = 7.20 Hz) 7.89 (1 H, br s) 7.70 (1 H, d, J = 1.00 Hz) 7.04-6.79 (2 H, m) 5.07-4.70 (1 H, m) 2.15 (1 H, dt, J = 13.85, 7.02 Hz) 1.73-1.61 (1 H, m) 1.25-1.16 (4 H, m); LCMS (electrospray) m/z 431.0 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(ethylamino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 497 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.78-13.23 (1 H, m) 11.18 (1 H, s) 8.66 (1 H, d, J = 7.20 Hz) 7.90 (1 H, s) 7.83-7.73 (1 H, m) 7.05-6.90 (2 H, m) 5.10-4.83 (1 H, m) 3.30 (4 H, q, J = 6.65 Hz) 2.15 (1 H, dt, J = 13.77, 6.98 Hz) 1.77-1.61 (1 H, m) 1.27-1.14 (1 H, m) 1.02 (6 H, t, J = 7.09 Hz); LCMS (electrospray) m/z 459.0 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(diethylamino)- 6-fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 498 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.53 (br s, 1H), 11.16 (s, 1H), 8.65 (d, J = 7.2 Hz, 1H), 7.90 (br s, 1H), 7.74 (d, J = 1.0 Hz, 1H), 6.95 (s, 1H), 6.93- 6.88 (m, 1H), 5.05-4.83 (m, 1H), 3.92-3.76 (m, 4H), 3.30-3.21 (m, 4H), 2.14 (td, J = 6.9, 13.9 Hz, 1H), 1.73-1.61 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 473.3 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- morpholino-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 499 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.24 (br s, 1H), 11.14 (s, 1H), 8.61 (d, J = 7.2 Hz, 1H), 7.89 (br s, 1H), 7.69 (d, J = 1.0 Hz, 1H), 6.92 (s, 1H), 6.88 (dd, J = 2.0, 7.1 Hz, 1H), 5.07-4.82 (m, 1H), 3.72 (br s, 4H), 2.19-2.10 (m, 1H), 1.99-1.90 (m, 4H), 1.74-1.61 (m, 1H), 1.23-1.12 (m, 1H); LCMS (electrospray) m/z 457.3 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (pyrrolidin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 500 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.61 (br s, 1H), 11.17 (s, 1H), 8.81 (br s, 2H), 8.67 (d, J = 7.1 Hz, 1H), 7.94 (br s, 1H), 7.73 (d, J = 1.0 Hz, 1H), 6.97 (s, 1H), 6.90 (dd, J = 1.9, 7.2 Hz, 1H), 5.08-4.81 (m, 1H), 3.62-3.40 (m, 8H), 2.22-2.09 (m, 1H), 1.74-1.59 (m, 1H), 1.26-1.11 (m, 1H); LCMS (electrospray) m/z 472.3 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (piperazin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 TFA 501 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.10 (br s, 1H), 11.14 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.88 (br s, 1H), 7.68 (d, J = 0.9 Hz, 1H), 6.92 (s, 1H), 6.88 (dd, J = 1.9, 7.1 Hz, 1H), 5.16-4.74 (m, 1H), 4.51-4.25 (m, 4H), 2.35 (quin, J = 7.3 Hz, 2H), 2.14 (td, J = 6.9, 13.9 Hz, 1H), 1.76-1.57 (m, 1H), 1.29-1.06 (m, 1H); LCMS (electrospray) m/z 443.3 (M + H)+. J (1S,2S)-N-(5-(7-(azetidin-1-yl)-5-chloro- 6-fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 502 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (br s, 1H), 11.17 (s, 1H), 9.37 (br s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.90 (br s, 1H), 7.74 (d, J = 1.0 Hz, 1H), 6.96 (s, 1H), 6.92 (dd, J = 2.0, 7.1 Hz, 1H), 5.05-4.84 (m, 1H), 3.13 (br s, 2H), 2.92 (d, J = 2.4 Hz, 3H), 2.72 (s, 3H), 2.70 (s, 3H), 2.14 (br d, J = 7.1 Hz, 1H), 2.02 (br s, 4H), 1.73-1.62 (m, 1H), 1.48 (br s, 4H), 1.23-1.13 (m, 1H); LCMS(electrospray) m/z542.3 (M + H+). J (1S,2S)-N-(5-(5-chloro-7-((4- (dimethylamino)cyclohexyl)(methyl)amino)- 6-fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 3 TFA 503 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.94-13.16 (m, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.90 (s, 1H), 7.82-7.71 (m, 1H), 7.84-7.70 (m, 1H), 7.04-6.85 (m, 2H), 5.09-4.82 (m, 1H), 3.44- 3.32 (m, 1H), 3.24-3.06 (m, 1H), 2.95-2.81 (m, 3H), 2.23-2.07 (m, 1H), 1.90-1.76 (m, 3H), 1.74- 1.34 (m, 6H), 1.26-1.07 (m, 3H); LCMS(electrospray) m/z 515.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((4- hydroxycyclohexyl)(methyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 3 TFA 504 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 8.37 (br s, 2H), 7.91 (s, 1H), 7.74 (d, J = 1.0 Hz, 1H), 6.96 (s, 1H), 6.92 (dd, J = 2.0, 7.2 Hz, 1H), 5.07-4.82 (m, 1H), 3.10 (br s, 1H), 2.91 (d, J = 2.6 Hz, 3H), 2.56- 2.52 (m, 5H), 2.15 (td, J = 6.9, 13.5 Hz, 1H), 2.06 (br d, J = 9.9 Hz, 2H), 1.99 (br d, J = 11.5 Hz, 2H), 1.72-1.61 (m, 1H), 1.54-1.44 (m, 2H), 1.38-1.26 (m, 2H), 1.21-1.14 (m, 1H); LCMS(electrospray) m/z 528.3 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl((1R,4R)-4- (methylamino)cyclohexyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 3 TFA 505 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35 (br s, 1H), 11.18 (s, 1H), 8.67 (d, J = 7.2 Hz, 1H), 8.33 (br s, 2H), 7.94 (s, 1H), 7.79-7.75 (m, 1H), 6.97 (s, 1H), 6.94 (dd, J = 2.0, 7.1 Hz, 1H), 5.06-4.84 (m, 1H), 3.08 (br s, 1H), 2.85 (s, 3H), 2.57 (t, J = 5.4 Hz, 3H), 2.54-2.52 (m, 2H), 2.15 (td, J = 7.2, 14.0 Hz, 1H), 1.83 (br s, 4H), 1.72-1.56 (m, 5H), 1.23-1.13 (m, 1H); LCMS(electrospray) m/z 528.3 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl((1S,4S)-4- (methylamino)cyclohexyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 3 TFA 506 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.33 (br s, 1H), 11.11 (s, 1H), 8.58 (d, J = 7.0 Hz, 1H), 7.71 (s, 1H), 7.57 (d, J = 0.9 Hz, 1H), 6.88 (s, 1H), 6.84-6.79 (m, 2H), 5.07-4.80 (m, 1H), 3.99 (s, 3H), 2.35 (s, 3H), 2.14 (td, J = 7.1, 14.0 Hz, 1H), 1.73-1.61 (m, 1H), 1.17 (tdd, J = 6.2, 8.9, 12.3 Hz, 1H); LCMS(electrospray) m/z 380.2 (M + H+). J (1S,2S)-2-fluoro-N-(5-(7-methoxy-5- methyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)cyclopropane-1- carboxamide. 2 TFA 507 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.76 (br s, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.94 (br s, 1H), 7.75 (d, J = 1.0 Hz, 1H), 6.95 (s, 1H), 6.92 (dd, J = 2.0, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 4.33 (br s, 2H), 4.27-4.20 (m, 1H), 3.81-3.74 (m, 1H), 3.69 (dt, J = 6.1, 7.6 Hz, 1H), 2.18-2.10 (m, 1H), 2.07- 1.98 (m, 1H), 1.92-1.81 (m, 2H), 1.80-1.73 (m, 1H), 1.72-1.62 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 488.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- ((tetrahydrofuran-2-yl)methoxy)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 508 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.30 (br s, 1H), 11.16 (s, 1H), 8.62 (br d, J = 7.1 Hz, 1H), 8.45 (br s, 2H), 7.85 (s, 1H), 7.70 (s, 1H), 6.93 (s, 1H), 6.89 (dd, J = 2.0, 7.1 Hz, 1H), 5.27 (br d, J = 8.9 Hz, 1H), 5.05-4.83 (m, 1H), 3.60 (br s, 1H), 2.99 (br s, 1H), 2.58 (br t, J = 5.2 Hz, 3H), 2.52 (br s, 1H), 2.18- 2.12 (m, 1H), 2.08 (br d, J = 9.8 Hz, 4H), 1.72-1.62 (m, 1H), 1.45-1.32 (m, 4H), 1.23-1.14 (m, 1H); J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((4- (methylamino)cyclohexyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 3 TFA 509 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.16 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.79 (s, 1H), 7.64 (d, J = 0.9 Hz, 1H), 6.91 (s, 1H), 6.85 (dd, J = 2.0, 7.1 Hz, 1H), 5.10-4.81 (m, 1H), 4.31 (br d, J = 6.8 Hz, 2H), 2.23 (d, J = 3.1 Hz, 3H), 2.14 (td, J = 6.9, 13.9 Hz, 1H), 1.73-1.61 (m, 1H), 1.39 (t, J = 7.0 Hz, 3H), 1.17 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 412.2 (M + H+). J (1S,2S)-N-(5-(7-ethoxy-6-fluoro-5- methyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 510 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.16-12.81 (m, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.84 (s, 1H), 7.72-7.66 (m, 1H), 6.95-6.86 (m, 2H), 6.00-5.59 (m, 2H), 5.17-4.76 (m, 1H), 2.21- 2.09 (m, 1H), 1.76-1.59 (m, 1H), 1.43-1.36 (m, 1H), 1.26-1.11 (m, 1H); LCMS(electrospray) m/z 403.1 (M + H+). J (1S,2S)-N-(5-(7-amino-5-chloro-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 511 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.28 (s, 1H), 11.12 (s, 1H), 8.58 (d, J = 7.1 Hz, 1H), 7.70 (d, J = 1.2 Hz, 1H), 7.57 (dd, J = 0.9, 1.7 Hz, 1H), 6.87 (s, 1H), 6.84-6.79 (m, 2H), 5.05-4.83 (m, 1H), 4.27 (q, J = 7.0 Hz, 2H), 2.34 (s, 3H), 2.19-2.09 (m, 1H), 1.72-1.61 (m, 1H), 1.46 (t, J = 7.0 Hz, 3H), 1.17 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 393.9 (M + H+). J (1S,2S)-N-(5-(7-ethoxy-5-methyl-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 512 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.27 (br s, 1H), 11.15 (s, 1H), 9.49 (br s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.88 (br s, 1H), 7.69 (d, J = 1.0 Hz, 1H), 6.93 (s, 1H), 6.90 (dd, J = 2.0, 7.2 Hz, 1H), 5.33 (br s, 1H), 5.11-4.77 (m, 1H), 3.19 (br d, J = 9.0 Hz, 1H), 2.77 (s, 3H), 2.76 (s, 3H), 2.52 (d, J = 2.0 Hz, 1H), 2.12 (br d, J = 11.7 Hz, 3H), 2.04 (br d, J = 10.8 Hz, 2H), 1.72-1.61 (m, 1H), 1.61-1.51 (m, 2H), 1.46- 1.32 (m, 2H), 1.17 (tdd, J = 6.2, 9.0, 12.4 Hz, 1H); LCMS(electrospray) m/z 528.3 (M + H+). J (1S,2S)-N-(5-(5-chloro-7-((4- (dimethylamino)cyclohexyl)amino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 3 TFA 513 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (s, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.76 (s, 1H), 7.64 (s, 1H), 6.93 (s, 1H), 6.82 (d, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 2.69-2.62 (m, 2H), 2.50 (s, 3H), 2.16-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.28- 1.12 (m, 1H), 1.12-1.08 (m, 3H); LCMS (electrospray) m/z 428.1 (M + H)+. J (1S,2S)-N-(5-(5-ethyl-6-fluoro-7- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide dihydrochloride. 2 HCl 514 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63-13.08 (m, 1H), 11.19 (s, 1H), 8.67 (td, J = 1.0, 7.1 Hz, 1H), 8.03-7.86 (m, 1H), 7.83-7.56 (m, 4H), 7.06- 6.86 (m, 2H), 5.14-4.81 (m, 2H), 3.24-3.15 (m, 1H), 2.95-2.84 (m, 4H), 2.15 (td, J = 7.0, 13.9 Hz, 1H), 2.02-1.91 (m, 2H), 1.86-1.74 (m, 2H), 1.73- 1.45 (m, 4H), 1.41-1.28 (m, 1H), 1.25-1.12 (m, 1H); LCMS(electrospray) m/z 514.1 (M + H+). J (1S,2S)-N-(5-7-((4- aminocyclohexyl)(methyl)amino)-5- chloro-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 3 TFA 515 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.32 (br d, J = 13.8 Hz, 1H), 11.16 (s, 1H), 8.63 (br d, J = 6.9 Hz, 1H), 7.95-7.60 (m, 5H), 6.99-6.79 (m, 2H), 5.35- 4.78 (m, 2H), 4.09-3.63 (m, 1H), 4.05-3.45 (m, 1H), 3.24-2.98 (m, 3H), 2.15 (td, J = 6.9, 13.7 Hz, 1H), 2.09-1.93 (m, 2H), 1.77 (br s, 3H), 1.72- 1.61 (m, 1H), 1.53-1.34 (m, 2H), 1.26-1.14 (m, 1H); LCMS(electrospray) m/z 500.4 (M + H+). J (1S,2S)-N-(5-(7-((4- aminocyclohexyl)amino)-5-chloro-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 3 TFA 516 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.54-12.40 (m, 1H), 11.16 (s, 1H), 8.62 (d, J = 7.3 Hz, 1H), 7.98-7.77 (m, 1H), 7.71 (br s, 1H), 7.02-6.86 (m, 2H), 6.84-6.66 (m, 1H), 5.07-4.82 (m, 1H), 3.47 (br s, 2H), 3.26 (br s, 1H), 2.15 (td, J = 6.8, 13.6 Hz, 1H), 1.99 (br d, J = 10.3 Hz, 1H), 1.82 (br d, J = 10.4 Hz, 1H), 1.74-1.62 (m, 4H), 1.55 (br d, J = 10.4 Hz, 1H), 1.39 (d, J = 5.1 Hz, 9H), 1.36-1.11 (m, 3H); LCMS(electrospray) m/z 600.1 (M + H+). J tert-butyl (4-((5-chloro-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7- yl)amino)cyclohexyl)carbamate. 2 TFA 517 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70-12.88 (m, 1H), 11.24-11.06 (m, 1H), 8.71-8.53 (m, 1H), 7.93-7.64 (m, 2H), 7.05-6.57 (m, 2H), 5.10-4.69 (m, 1H), 3.92-3.72 (m, 3H), 2.27-2.08 (m, 1H), 1.81-1.45 (m, 8H), 1.34-1.09 (m, 2H); LCMS(electrospray) m/z 501.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((4- hydroxycyclohexyl)amino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 518 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (br s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.68 (br s, 1H), 7.62 (s, 1H), 6.91 (s, 1H), 6.83 (dd, J = 1.8, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 3.26 (br d, J = 6.1 Hz, 4H), 2.61 (br d, J = 7.1 Hz, 2H), 2.19-2.10 (m, 1H), 1.74-1.60 (m, 1H), 1.21-1.14 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H), 0.99 (t, J = 7.1 Hz, 6H); LCMS(electrospray) m/z 453.4(M + H+). J (1S,2S)-N-(5-(7-(diethylamino)-5-ethyl-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 519 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.99-12.38 (m, 1H), 11.14 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.68 (s, 1H), 7.58 (d, J = 0.9 Hz, 1H), 6.90 (s, 1H), 6.79 (dd, J = 1.9, 7.0 Hz, 1H), 5.11-4.76 (m, 1H), 2.97 (s, 3H), 2.97 (s, 3H), 2.65-2.53 (m, 2H), 2.14 (td, J = 6.9, 13.8 Hz, 1H), 1.75-1.60 (m, 1H), 1.22- 1.14 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z425.2 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-5-ethyl- 6-fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 520 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.79 (br s, 1H), 11.18 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 7.99 (br s, 1H), 7.80 (d, J = 0.7 Hz, 1H), 6.98 (s, 1H), 6.96 (dd, J = 1.9, 7.2 Hz, 1H), 5.06-4.82 (m, 1H), 3.53 (t, J = 6.7 Hz, 2H), 3.12-3.04 (m, 2H), 2.15 (td, J = 7.1, 13.8 Hz, 1H), 1.73-1.61 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 464 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((2- hydroxyethyl)thio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 521 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.62 (s, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 8.07 (d, 1H), 7.78 (s, 1H), 7.65 (d, 1H), 6.94 (s, 1H), 6.83 (dd, 1H), 5.08-4.83 (m, 1H), 3.64 (s, 2H), 2.63 (d, 2H), 2.60 (d, 3H), 2.20-2.11 (m, 1H), 1.75-1.61 (m, 1H), 1.24-1.15 (m, 1H), 1.11 (t, 3H); LCMS(electrospray) m/z 485.2 (M + H+). J (1S,2S)-N-(5-(5-ethyl-6-fluoro-7-((2- (methylamino)-2-oxoethyl)thio)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide bis(2,2,2-trifluoroacetate). 2 TFA 522 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.72-13.26 (m, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.78 (s, 1H), 7.64 (d, J = 0.8 Hz, 1H), 6.95 (s, 1H), 6.82 (dd, J = 1.9, 7.1 Hz, 1H), 5.13-4.76 (m, 1H), 3.97 (s, 2H), 3.02 (s, 3H), 2.83 (s, 3H), 2.66-2.59 (m, 2H), 2.19-2.08 (m, 1H), 1.74-1.61 (m, 1H), 1.23-1.15 (m, 1H), 1.11 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 499.4 (M + H+). J (1S,2S)-N-(5-7-((2-(dimethylamino)-2- oxoethyl)thio)-5-ethyl-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide bis(2,2,2-trifluoroacetate). 2 TFA 523 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.46 (s, 1H), 11.16 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.84 (s, 1H), 7.68 (d, J = 0.7 Hz, 1H), 6.93 (s, 1H), 6.88 (dd, J = 2.0, 7.1 Hz, 1H), 5.08-4.81 (m, 2H), 3.51 (t, J = 6.9 Hz, 2H), 3.01 (br t, J = 6.8 Hz, 2H), 2.24 (d, J = 2.9 Hz, 3H), 2.15 (td, J = 6.9, 14.0 Hz, 1H), 1.73- 1.61 (m, 1H), 1.17 (tdd, J = 6.2, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 444.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2- hydroxyethyl)thio)-5-methyl-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 524 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.13 (s, 1H), 8.58 (d, J = 7.1 Hz, 1H), 7.67 (s, 1H), 7.55 (d, J = 0.8 Hz, 1H), 6.88 (s, 1H), 6.78 (dd, J = 1.9, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 3.50 (q, J = 7.0 Hz, 2H), 2.60 (br d, J = 7.6 Hz, 2H), 2.14 (td, J = 7.2, 13.9 Hz, 1H), 1.74-1.59 (m, 1H), 1.22-1.07 (m, 7H); LCMS(electrospray) m/z 425.2 (M + H+). J (1S,2S)-N-(5-(5-ethyl-7-(ethylamino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 525 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48-12.86 (m, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.0 Hz, 1H), 7.68 (s, 1H), 7.60 (d, J = 0.9 Hz, 1H), 6.91 (s, 1H), 6.81 (dd, J = 1.9, 7.0 Hz, 1H), 5.08-4.79 (m, 1H), 3.23 (q, J = 7.0 Hz, 2H), 2.95 (d, J = 1.6 Hz, 3H), 2.60 (br d, J = 7.1 Hz, 2H), 2.18-2.10 (m, 1H), 1.72-1.61 (m, 1H), 1.20-1.14 (m, 1H), 1.12-1.04 (m, 6H); LCMS(electrospray) m/z 439.2 (M + H+). J (1S,2S)-N-(5-(5-ethyl-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 526 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70-13.32 (m, 1H), 13.12-12.20 (m, 1H), 11.17 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.79 (s, 1H), 7.65 (d, J = 0.9 Hz, 1H), 6.94 (s, 1H), 6.83 (dd, J = 2.0, 7.1 Hz, 1H), 5.07-4.82 (m, 1H), 3.77 (br s, 2H), 2.63 (br d, J = 6.8 Hz, 2H), 2.21-2.09 (m, 1H), 1.74-1.61 (m, 1H), 1.24-1.14 (m, 1H), 1.10 (t, J = 7.4 Hz, 3H); LCMS(electrospray) m/z 472.1 (M + H+). J 2-((5-ethyl-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7-yl)thio)acetic acid. 2 TFA 527 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64-13.45 (m, 1H), 11.24-11.12 (m, 1H), 8.72-8.62 (m, 1H), 8.02-7.73 (m, 4H), 7.03-6.89 (m, 2H), 5.13-4.83 (m, 1H), 2.88 (br d, J = 17.4 Hz, 2H), 2.08 (s, 5H), 2.04-1.93 (m, 2H), 1.75-1.58 (m, 3H), 1.28-1.18 (m, 3H); LCMS(electrospray) m/z 500.1 (M + H+). J (1S,2S)-N-(5-(7-((3- aminocyclopentyl)(methyl)amino)-5- chloro-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 2 TFA 528 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.75 (s, 1H), 7.88 (s, 1H), 7.82-7.76 (m, 1H), 7.74-7.68 (m, 1H), 2.19-2.11 (m, 1H), 1.92-1.81 (m, 1H), 1.35-1.22 (m, 2H); LCMS(electrospray) m/z 404.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- hydroxy-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 2 TFA 529 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68 (s, 1H), 11.16 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.88 (d, J = 1.3 Hz, 1H), 7.68 (d, J = 1.0 Hz, 1H), 6.94 (s, 1H), 6.90 (dd, J = 1.8, 7.1 Hz, 1H), 5.07-4.82 (m, 1H), 2.54 (s, 3H), 2.28 (s, 3H), 2.19-2.10 (m, 1H), 1.79- 1.57 (m, 1H), 1.26-1.12 (m, 1H); LCMS(electrospray) m/z 446.0 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5,7- bis(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 2 TFA 530 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 13.40 (br s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.81 (s, 1H), 7.67 (dd, J = 0.7, 1.7 Hz, 1H), 7.52 (dd, J = 0.9, 9.3 Hz, 1H), 6.93 (s, 1H), 6.90 (dd, J = 1.8, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 2.26 (s, 3H), 2.15 (td, J = 7.0, 13.9 Hz, 1H), 1.75-1.61 (m, 1H), 1.21-1.14 (m, 1H); LCMS(electrospray) m/z 400.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 531 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.48 (s, 1H), 11.16 (s, 1H), 8.63 (d, J = 6.8 Hz, 1H), 7.72 (s, 1H), 7.61 (s, 1H), 6.92 (s, 1H), 6.81 (dd, J = 7.2, 2.0 Hz, 1H), 5.04-4.85 (m, 1H), 4.34-4.29 (m, 2H), 2.64- 2.60 (m, 2H), 2.17-2.13 (m, 1H), 1.75-1.65 (m, 1H), 1.40 (t, J = 7.2 Hz, 3H), 1.19-1.15 (m, 1H), 1.12 (t, J = 7.2 Hz, 3H); LCMS(electrospray) m/z 426.2 (M + H+). J (1S,2S)-N-(5-(7-ethoxy-5-ethyl-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 2 TFA 532 embedded image .sup.1H NMR (400 MHz, CHLOROFORM-d) δ 8.46- 8.41 (m, 1 H), 8.37 (d, J = 7.09 Hz, 1 H), 7.80-7.74 (m, 1 H), 7.45 (d, J = 0.86 Hz, 1 H), 7.09 (s, 1 H), 6.73 (dd, J = 7.03, 1.90 Hz, 1 H), 5.00-4.72 (m, 1 H), 2.81-2.64 (m, 2 H), 2.01-1.94 (m, 1 H), 1.92- 1.89 (m, 1 H), 1.28-1.25 (m, 1 H), 1.18 (t, J = 7.46 Hz, 3 H); LCMS(electrospray) m/z 400.0 (M + H+). J (1S,2S)-N-(5-(5-ethyl-6,7-difluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 2 TFA 533 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.18 (s, 1H), 8.67 (d, J = 7.0 Hz, 1H), 7.91 (s, 1H), 7.71 (s, 1H), 6.96 (s, 1H), 6.89 (dd, J = 1.9, 7.1 Hz, 1H), 5.15- 4.65 (m, 1H), 3.13 (s, 3H), 2.24 (d, J = 2.8 Hz, 3H), 2.15 (td, J = 7.0, 14.1 Hz, 1H), 1.76-1.58 (m, 1H), 1.26-1.10 (m, 1H); LCMS(electrospray) m/z 429.11 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylsulfinyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 534 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.39 (br s, 1H), 14.04-12.74 (m, 1H), 11.15 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.80 (s, 1H), 7.64 (d, J = 0.9 Hz, 1H), 7.29 (dd, J = 2.0, 7.3 Hz, 1H), 6.96-6.90 (m, 1H), 6.86 (dd, J = 1.8, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 4.30 (br t, J = 4.9 Hz, 2H), 3.78 (t, J = 5.1 Hz, 2H), 2.24 (d, J = 3.1 Hz, 3H), 2.20-2.08 (m, 1H), 1.75- 1.58 (m, 1H), 1.25-1.13 (m, 1H); LCMS(electrospray) m/z 428.0 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-(2- hydroxyethoxy)-5-methyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. TFA 535 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.41 (d, J = 7.1 Hz, 1H), 7.66 (s, 1H), 7.44 (s, 1H), 6.83 (s, 1H), 6.74 (dd, J = 1.7, 7.1 Hz, 1H), 4.86 (td, J = 3.1, 6.3 Hz, 1H), 4.69 (dt, J = 3.9, 6.2 Hz, 1H), 4.46- 4.38 (m, 2H), 4.33-4.25 (m, 2H), 3.89-3.80 (m, 1H), 2.20-2.16 (m, 1H), 2.18 (d, J = 3.2 Hz, 2H), 2.00 (td, J = 6.9, 13.8 Hz, 1H), 1.78-1.62 (m, 1H), 1.19-1.04 (m, 1H); LCMS(electrospray) m/z 471.1 (M + H+). J 2-((6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 5-methyl-1H-indazol-7-yl)oxy)ethyl carbamate 536 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.19 (s, 1H), 8.67 (d, J = 7.2 Hz, 1H), 7.67 (s, 1H), 6.96 (s, 1H), 6.87 (s, 1H), 6.79 (dd, J = 2.0, 7.2 Hz, 1H), 5.08- 4.79 (m, 1H), 2.19-2.08 (m, 1H), 1.74-1.59 (m, 1H), 1.28-1.09 (m, 2H); LCMS(electrospray) m/z 406.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6,7-difluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide. 1 TFA 537 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31 (br s, 1H), 11.27-11.11 (m, 1H), 10.14 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.91 (s, 1H), 7.80 (d, J = 0.9 Hz, 1H), 6.97 (s, 1H), 6.95 (dd, J = 1.9, 7.2 Hz, 1H), 5.09- 4.82 (m, 1H), 2.18 (s, 3H), 2.16-2.10 (m, 1H), 1.75-1.61 (m, 1H), 1.18 (ddd, J = 2.7, 6.1, 12.5 Hz, 1H); LCMS(electrospray) m/z 445.2 (M + H+). J (1S,2S)-N-(5-(7-acetamido-5-chloro-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide. 1 TFA 538 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.73 (br s, 1H), 11.22 (s, 1H), 8.72 (d, J = 7.0 Hz, 1H), 8.06 (s, 1H), 7.83 (d, J = 1.0 Hz, 1H), 7.01 (s, 1H), 6.97 (dd, J = 2.0, 7.2 Hz, 1H), 5.08-4.83 (m, 1H), 3.20 (s, 3H), 2.16 (td, J = 7.0, 14.0 Hz, 1H), 1.75-1.60 (m, 1H), 1.24-1.13 (m, 1H); LCMS(electrospray) m/z 450 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methylsulfinyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 539 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.15 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.80 (s, 1H), 7.63 (d, J = 0.7 Hz, 1H), 6.91 (s, 1H), 6.85 (dd, J = 1.9, 7.2 Hz, 1H), 6.06-5.88 (m, 1H), 5.05-4.82 (m, 1H), 4.33 (br t, J = 5.4 Hz, 2H), 3.62 (br t, J = 5.8 Hz, 5H), 2.94 (s, 3H), 2.23 (d, J = 3.1 Hz, 3H), 2.18-2.11 (m, 1H), 1.73-1.61 (m, 1H), 1.20-1.14 (m, 1H); LCMS(electrospray) m/z 484.4 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(2-(1-methylureido)ethoxy)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 540 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.95 (s, 1H), 11.16 (s, 1H), 9.93 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.76 (s, 1H), 7.67 (s, 1H), 6.93 (s, 1H), 6.87 (dd, J = 1.7, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 2.24 (d, J = 2.6 Hz, 3H), 2.20-2.10 (m, 4H), 1.73-1.60 (m, 1H), 1.17 (tdd, J = 6.4, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 424.15 (M + H+). J (1S,2S)-N-(5-(7-acetamido-6-fluoro-5- methyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 541 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.96 (br s, 1H), 7.66 (d, J = 1.0 Hz, 1H), 6.94 (s, 1H), 6.88 (dd, J = 2.0, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 2.30 (s, 3H), 2.15 (td, J = 7.0, 14.0 Hz, 1H), 1.74-1.60 (m, 1H), 1.17 (tdd, J = 6.3, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 418 (M + H+). J (1S,2S)-N-(5-(6,7-difluoro-5-(methylthio)- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide. 1 TFA 542 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.97 (s, 1H), 11.16 (s, 1H), 8.63 (d, J = 7.2 Hz, 1H), 8.35 (s, 1H), 7.88 (s, 1H), 7.71 (s, 1H), 6.93 (s, 1H), 6.89 (d, J = 7.2 Hz, 1H), 5.04-4.85 (m, 1H), 3.23 (s, 3H), 2.16- 2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 532.1 (M + H)+. J tert-butyl 2-(5-chloro-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7-yl)-1-methylhydrazine-1- carboxylate 543 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.02-13.34 (m, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.0 Hz, 1H), 7.85 (s, 1H), 7.65 (s, 1H), 6.93 (s, 1H), 6.89 (dd, J = 1.8, 7.1 Hz, 1H), 5.11-4.78 (m, 1H), 4.35 (q, J = 7.0 Hz, 2H), 2.28 (s, 3H), 2.19-2.12 (m, 1H), 1.68 (m, J = 3.2, 6.8, 19.9 Hz, 1H), 1.41 (t, J = 7.0 Hz, 3H), 1.26-1.11 (m, 1H); LCMS(electrospray) m/z 444.2 (M + H+). J (1S,2S)-N-(5-(7-ethoxy-6-fluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 544 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.15 (s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.80 (s, 1H), 7.64 (d, J = 1.0 Hz, 1H), 6.91 (s, 1H), 6.85 (dd, J = 1.9, 7.1 Hz, 1H), 6.28 (br s, 1H), 5.14-4.71 (m, 1H), 4.22 (t, J = 5.4 Hz, 2H), 3.40 (br d, J = 4.1 Hz, 2H), 2.24 (d, J = 3.0 Hz, 3H), 2.19-2.09 (m, 1H), 1.73-1.59 (m, 1H), 1.24-1.07 (m, 1H); LCMS(electrospray) m/z 470.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(2-ureidoethoxy)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 545 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.24-11.04 (m, 1H), 8.74-8.52 (m, 1H), 7.85-7.75 (m, 1H), 7.64 (d, J = 0.9 Hz, 1H), 6.91 (s, 1H), 6.85 (dd, J = 1.8, 7.1 Hz, 1H), 6.27-6.15 (m, 1H), 6.03-5.80 (m, 1H), 5.09-4.80 (m, 1H), 4.31-4.12 (m, 2H), 3.47- 3.34 (m, 2H), 2.57 (s, 3H), 2.23 (d, J = 3.1 Hz, 3H), 2.19-2.08 (m, 1H), 1.75-1.60 (m, 1H), 1.25- 1.10 (m, 1H); LCMS(electrospray) m/z 484.2 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(2-(3-methylureido)ethoxy)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 546 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52-13.40 (m, 1H), 11.16 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.85 (br s, 1H), 7.68 (s, 1H), 6.94 (s, 1H), 6.89 (dd, J = 1.6, 7.0 Hz, 1H), 5.04-4.83 (m, 1H), 4.05 (br t, J = 6.7 Hz, 2H), 3.16 (br d, J = 5.5 Hz, 2H), 2.53 (br s, 3H), 2.25 (d, J = 2.7 Hz, 3H), 2.17-2.13 (m, 1H), 2.04 (td, J = 2.4, 4.9 Hz, 1H), 1.68 (tdd, J = 3.3, 6.6, 19.7 Hz, 1H), 1.17 (ddd, J = 2.6, 6.2, 12.3 Hz, 1H); LCMS(electrospray) m/z 501.2 (M + H+). J 2-((6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 5-methyl-1H-indazol-7-yl)thio)ethyl methylcarbamate. 1 TFA 547 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67-13.25 (m, 1H), 11.16 (s, 1H), 9.63 (br t, J = 5.2 Hz, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.82 (s, 1H), 7.64 (d, J = 0.9 Hz, 1H), 6.92 (s, 1H), 6.85 (dd, J = 1.9, 7.2 Hz, 1H), 5.07-4.83 (m, 1H), 4.38 (s, 2H), 3.66 (q, J = 5.5 Hz, 3H), 2.23 (d, J = 3.1 Hz, 3H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.75-1.61 (m, 1H), 1.18-1.29 (m, J = 2.9, 6.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 523.3 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(2-(2,2,2-trifluoroacetamido)ethoxy)- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 548 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.32 (s, 1H), 11.19 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.89 (s, 1H), 7.73 (s, 1H), 6.96 (s, 1H), 6.89 (dd, J = 1.8, 7.1 Hz, 1H), 5.15-4.72 (m, 1H), 3.98 (s, 3H), 2.24 (d, J = 2.9 Hz, 3H), 2.20-2.09 (m, 1H), 1.76-1.59 (m, 1H), 1.18 (ddd, J = 2.8, 6.2, 12.2 Hz, 1H); LCMS(electrospray) m/z 426.2 (M + H+). J methyl 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 5-methyl-1H-indazole-7-carboxylate 549 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.66-13.38 (m, 1H), 13.19 (br s, 1H), 11.19 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.85 (s, 1H), 7.72 (s, 1H), 6.96 (s, 1H), 6.89 (dd, J = 1.8, 7.1 Hz, 1H), 5.07-4.84 (m, 1H), 2.24 (d, J = 3.1 Hz, 3H), 2.18-2.13 (m, 1H), 1.72-1.62 (m, 1H), 1.20-1.14 (m, 1H); LCMS(electrospray) m/z 412.2 (M + H+). J 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 5-methyl-1H-indazole-7-carboxylic acid. 1 TFA 550 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.22-11.13 (m, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.95-7.87 (m, 1H), 7.72-7.70 (m, 1H), 6.96-6.93 (m, 1H), 6.92-6.89 (m, 1H), 5.07-4.81 (m, 1H), 3.21 (s, 3H), 2.30- 2.25 (m, 3H), 2.25-2.23 (m, 1H), 2.20-2.09 (m, 1H), 1.79 (s, 3H), 1.74-1.63 (m, 1H), 1.28-1.09 (m, 1H); LCMS(electrospray) m/z 438.16 (M + H+) J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(N-methylacetamido)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide. 1 TFA 551 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.20 (s, 1H), 8.70 (d, J = 7.1 Hz, 1H), 7.99 (s, 1H), 7.83 (d, J = 0.9 Hz, 1H), 7.03-6.95 (m, 2H), 5.10- 4.82 (m, 1H), 2.22-2.09 (m, 1H), 1.79-1.60 (m, 1H), 1.26-1.11 (m, 1H); LCMS(electrospray) m/z 432.2 (M + H+). J 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazole-7-carboxylic acid. 1 TFA 552 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.07-13.87 (m, 1H), 11.19 (s, 1H), 8.69 (br d, J = 7.1 Hz, 1H), 8.07-8.01 (m, 1H), 7.82 (d, J = 0.7 Hz, 1H), 6.99 (s, 1H), 6.97 (br d, J = 2.0 Hz, 1H), 5.05-4.83 (m, 1H), 3.23 (s, 3H), 2.18-2.11 (m, 1H), 1.82 (s, 3H), 1.71-1.64 (m, 1H), 1.22-1.13 (m, 1H); LCMS(electrospray) m/z 459.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(N- methylacetamido)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide. 1 TFA 553 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 12.95 (s, 1H), 11.15 (s, 1H), 8.60 (d, J = 7.2 Hz, 1H), 7.77 (s, 1H), 7.68 (s, 1H), 7.42 (s, 1H), 6.91-6.88 (m, 2H), 5.02 (s, 1H), 5.04-4.85 (m, 1H), 2.66 (s, 3H), 2.16- 2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 432.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(2- methylhydrazineyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 554 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.22 (s, 1H), 8.71 (d, J = 7.1 Hz, 1H), 8.05 (s, 1H), 7.85 (d, J = 1.0 Hz, 1H), 7.00 (s, 1H), 6.97 (dd, J = 2.0, 7.2 Hz, 1H), 5.08-4.81 (m, 1H), 4.00 (s, 3H), 2.19-2.11 (m, 1H), 1.75-1.60 (m, 1H), 1.21-1.13 (m, 1H); LCMS(electrospray) m/z 446.0 (M + H+). J methyl 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazole-7-carboxylate 555 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (br s, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.0 Hz, 1H), 7.89 (s, 1H), 7.77 (s, 1H), 7.04-6.89 (m, 2H), 5.15-4.82 (m, 1H), 4.58 (d, J = 4.3 Hz, 1H), 4.08 (br d, J = 5.4 Hz, 1H), 3.70 (br s, 1H), 2.90 (s, 3H), 2.11 (dt, J = 7.0, 13.6 Hz, 2H), 1.81-1.62 (m, 5H), 1.59-1.43 (m, 2H), 1.25-1.13 (m, 1H); LCMS(electrospray) m/z 501.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((3- hydroxycyclopentyl)(methyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 556 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.88-13.56 (m, 1H), 11.20 (s, 1H), 8.70 (d, J = 7.1 Hz, 1H), 8.00 (s, 1H), 7.82 (d, J = 0.7 Hz, 1H), 6.99 (s, 1H), 6.96 (d, J = 2.0 Hz, 1H), 5.05-4.85 (m, 1H), 3.13 (s, 3H), 2.93 (s, 3H), 2.18-2.11 (m, 1H), 1.72- 1.62 (m, 1H), 1.18 (ddd, J = 2.9, 6.1, 12.3 Hz, 1H); LCMS(electrospray) m/z459.1(M + H+). J 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N,N-dimethyl-1H-indazole-7-carboxamide 557 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.18 (br d, J = 2.5 Hz, 1H), 11.14 (s, 1H), 8.62 (d, J = 7.2 Hz, 1H), 7.74 (s, 1H), 7.62 (s, 1H), 6.90 (s, 1H), 6.87-6.81 (m, 1H), 5.17-4.73 (m, 2H), 3.65-3.57 (m, 2H), 3.28-3.18 (m, 2H), 2.97 (d, J = 2.3 Hz, 3H), 2.25- 2.10 (m, 4H), 1.76-1.58 (m, 1H), 1.26-1.11 (m, 1H); LCMS(electrospray) m/z 441.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7-((2- hydroxyethyl)(methyl)amino)-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 558 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43 (br s, 1H), 11.14 (s, 1H), 8.59 (d, J = 7.0 Hz, 1H), 7.78 (s, 1H), 7.62 (s, 1H), 6.91 (s, 1H), 6.87 (dd, J = 1.9, 7.1 Hz, 1H), 5.06-4.82 (m, 1H), 2.97 (d, J = 2.0 Hz, 6H), 2.26 (s, 3H), 2.19-2.10 (m, 1H), 1.73-1.61 (m, 1H), 1.22-1.12 (m, 1H); LCMS(electrospray) m/z 443 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 559 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.29 (br s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.0 Hz, 1H), 7.86 (br s, 1H), 7.71 (s, 1H), 7.00-6.86 (m, 2H), 5.44 (br s, 1H), 5.11-4.94 (m, 1H), 4.90-4.77 (m, 1H), 4.40- 4.11 (m, 2H), 2.25-2.09 (m, 2H), 2.04-1.86 (m, 1H), 1.84-1.57 (m, 5H), 1.30-1.08 (m, 1H); LCMS(electrospray) m/z 487.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((3- hydroxycyclopentyl)amino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 560 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.68-13.53 (m, 1H), 11.24-11.17 (m, 1H), 8.70 (d, J = 7.1 Hz, 1H), 8.67-8.60 (m, 1H), 7.99-7.93 (m, 1H), 7.81 (d, J = 0.9 Hz, 1H), 6.99 (s, 1H), 6.97-6.92 (m, 1H), 5.07-4.81 (m, 1H), 2.91 (d, J = 4.4 Hz, 3H), 2.20-2.10 (m, 1H), 1.75-1.55 (m, 1H), 1.07 (s, 1H); LCMS(electrospray) m/z 445.1(M + H+). J 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N-methyl-1H-indazole-7-carboxamide 561 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.18 (br s, 1H), 8.65 (d, J = 7.2 Hz, 1H), 7.88 (s, 1H), 7.76 (s, 1H), 7.09-6.87 (m, 2H), 5.08-4.84 (m, 1H), 3.87-3.71 (m, 1H), 3.59-3.43 (m, 1H), 3.60-3.42 (m, 1H), 2.89-2.81 (m, 3H), 2.46-2.39 (m, 2H), 2.21-2.09 (m, 1H), 2.24-2.07 (m, 1H), 2.20-1.95 (m, 1H), 1.99 (br d, J = 4.9 Hz, 1H), 1.79-1.62 (m, 3H), 1.26-1.12 (m, 2H); LCMS(electrospray) m/z 487.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((3- hydroxycyclobutyl)(methyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 562 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.11 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.83 (s, 1H), 7.65 (s, 1H), 6.91 (s, 1H), 6.86 (dd, J = 1.9, 7.1 Hz, 1H), 2.24 (d, J = 2.9 Hz, 3H), 2.00-1.87 (m, 1H), 0.88-0.77 (m, 4H); LCMS(electrospray) m/z 395.12 (M + H+). J N-(5-(6-fluoro-5-methyl-7-(methylthio)- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropanecarboxamide 563 embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.55- 8.47 (m, 1H), 7.79-7.72 (m, 1H), 7.58-7.54 (m, 1H), 7.00-6.93 (m, 1H), 6.89-6.83 (m, 1H), 5.02- 4.93 (m, 1H), 4.60-4.56 (m, 1H), 3.29-3.24 (m, 2H), 3.01-2.94 (m, 3H), 2.33-2.25 (m, 3H), 2.17- 2.07 (m, 1H), 1.89-1.77 (m, 1H), 1.27-1.19 (m, 1H), 1.15-1.09 (m, 3H); LCMS(electrospray) m/z 425.2 (M + H+). J (1S,2S)-N-(5-(7-(ethyl(methyl)amino)-6- fluoro-5-methyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 564 00embedded image .sup.1H NMR (400 MHz, METHANOL-d.sub.4) δ 8.43- 8.38 (m, 1H), 7.77-7.72 (m, 1H), 7.59-7.54 (m, 1H), 6.89-6.86 (m, 1H), 6.85-6.81 (m, 1H), 4.88- 4.82 (m, 1H), 4.72-4.64 (m, 1H), 3.20-3.15 (m, 2H), 3.20 (br s, 1H), 2.90 (d, J = 1.8 Hz, 2H), 2.95- 2.88 (m, 1H), 2.04-1.94 (m, 1H), 1.78-1.65 (m, 1H), 1.17-1.07 (m, 1H), 1.05-0.99 (m, 3H); LCMS(electrospray) m/z 445.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-7- (ethyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 565 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.18 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 7.80 (d, J = 4.8 Hz, 1H), 7.62 (d, J = 0.9 Hz, 1H), 6.92 (s, 1H), 6.80 (dd, J = 1.9, 7.1 Hz, 1H), 5.08-4.70 (m, 1H), 3.02 (d, J = 2.3 Hz, 6H), 2.20-2.12 (m, 1H), 1.73-1.62 (m, 1H), 1.22-1.14 (m, 1H); LCMS(electrospray) m/z 465.1 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-5-(trifluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 566 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (br s, 1H), 11.19 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.86 (s, 1H), 7.73 (s, 1H), 6.97 (s, 1H), 6.89 (dd, J = 1.9, 7.2 Hz, 1H), 5.07-4.80 (m, 1H), 2.74 (d, J = 6.4 Hz, 3H), 2.28 (d, J = 3.2 Hz, 3H), 2.20-2.09 (m, 1H), 1.74- 1.61 (m, 1H), 1.25-1.13 (m, 1H); LCMS(electrospray) m/z 409.14 (M + H+). J (1S,2S)-N-(5-(7-acetyl-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 567 03embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.28 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.83 (s, 1H), 7.67 (s, 1H), 6.89 (s, 1H), 6.87 (d, J = 1.8 Hz, 1H), 5.03-4.81 (m, 1H), 2.23 (d, J = 2.8 Hz, 3H), 1.64- 1.45 (m, 1H), 1.27 (qd, J = 6.5, 13.1 Hz, 1H); LCMS(electrospray) m/z 413.11 (M + H+). J (1S,2R)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 568 04embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.28 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.83 (s, 1H), 7.67 (d, J = 0.7 Hz, 1H), 6.88 (s, 1H), 6.87 (d, J = 1.8 Hz, 1H), 5.04-4.79 (m, 1H), 2.49-2.40 (m, 3H), 2.23 (d, J = 2.8 Hz, 3H), 1.62-1.45 (m, 1H), 1.27 (qd, J = 6.4, 13.1 Hz, 1H); LCMS(electrospray) m/z 413.11 (M + H+). J (1R,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 569 05embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.45 (br s, 1H), 11.10 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.81 (s, 1H), 7.66 (s, 1H), 7.52 (d, J = 9.3 Hz, 1H), 6.91 (s, 1H), 6.88 (dd, J = 1.8, 7.1 Hz, 1H), 2.26 (s, 3H), 2.00- 1.88 (m, 1H), 0.90-0.77 (m, 4H); LCMS(electrospray) m/z 382.1(M + H+) J N-(5-(6-fluoro-5-(methylthio)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropanecarboxamide 570 06embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43 (br s, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.1 Hz, 1H), 7.84 (s, 1H), 7.73-7.67 (m, 1H), 6.94 (s, 1H), 6.89 (dd, J = 2.0, 7.1 Hz, 1H), 5.16-4.74 (m, 1H), 3.12 (s, 3H), 2.92 (s, 3H), 2.24 (d, J = 2.9 Hz, 3H), 2.19-2.10 (m, 1H), 1.74-1.60 (m, 1H), 1.18 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 439.2 (M + H+). J 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N,N,5-trimethyl-1H-indazole-7- carboxamide 571 07embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (br s, 1H), 11.28 (br s, 1H), 8.63 (d, J = 7.1 Hz, 1H), 7.81 (s, 1H), 7.67 (s, 1H), 7.52 (d, J = 9.3 Hz, 1H), 6.93- 6.87 (m, 2H), 5.05-4.81 (m, 1H), 2.48-2.42 (m, 1H), 2.26 (s, 3H), 1.61-1.46 (m, 1H), 1.33-1.20 (m, 1H); LCMS(electrospray) m/z 400.1(M + H+). J (1R,2S)-2-fluoro-N-(5-(6-fluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 572 08embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.40 (br s, 1H), 11.28 (s, 1H), 8.63 (d, J = 7.0 Hz, 1H), 7.81 (s, 1H), 7.67 (s, 1H), 7.52 (d, J = 9.2 Hz, 1H), 6.93-6.87 (m, 2H), 5.03-4.80 (m, 1H), 2.46-2.42 (m, 1H), 2.26 (s, 3H), 1.61-1.46 (m, 1H), 1.27 (qd, J = 6.3, 13.0 Hz, 1H); LCMS(electrospray) m/z 400.1(M + H+). J (1S,2R)-2-fluoro-N-(5-(6-fluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 573 09embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.42 (br s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.0 Hz, 1H), 7.82 (s, 1H), 7.68 (s, 1H), 7.52 (d, J = 9.4 Hz, 1H), 6.93 (s, 1H), 6.90 (dd, J = 1.8, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 2.26 (s, 3H), 2.15 (td, J = 7.1, 14.1 Hz, 1H), 1.74- 1.61 (m, 1H), 1.22-1.12 (m, 1H); LCMS(electrospray) m/z 400.1(M + H+). J (1R,2R)-2-fluoro-N-(5-(6-fluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 574 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.47 (br s, 1H), 11.16 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.84 (s, 1H), 7.67 (s, 1H), 6.93 (s, 1H), 6.87 (dd, J = 1.8, 7.1 Hz, 1H), 5.08-4.79 (m, 1H), 3.30 (s, 3H), 2.25-2.23 (m, 1H), 2.24 (d, J = 2.9 Hz, 3H), 2.14 (br dd, J = 6.0, 8.1 Hz, 1H), 1.76-1.60 (m, 1H), 1.24-1.13 (m, 1H); LCMS(electrospray) m/z 413.11 (M + H+). J (1R,2R)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 575 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.74 (s, 1H), 11.22 (s, 1H), 8.72 (d, J = 7.1 Hz, 1H), 8.40 (s, 1H), 8.02 (s, 1H), 7.85 (d, J = 1.0 Hz, 1H), 7.02 (s, 1H), 6.97 (dd, J = 1.9, 7.2 Hz, 1H), 5.14-4.76 (m, 1H), 2.77 (d, J = 6.1 Hz, 3H), 2.21-2.12 (m, 1H), 1.75- 1.61 (m, 1H), 1.26-1.12 (m, 2H); LCMS(electrospray) m/z 430.3 (M + H+). J (1S,2S)-N-(5-(7-acetyl-5-chloro-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 576 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70-13.43 (m, 1H), 11.22 (s, 1H), 8.71 (d, J = 6.8 Hz, 1H), 8.08 (s, 2H), 7.95 (s, 1H), 7.82 (s, 1H), 7.03-6.91 (m, 2H), 5.10-4.81 (m, 1H), 2.15 (d, J = 6.8 Hz, 1H), 1.76-1.59 (m, 1H), 1.18 (d, J = 7.2 Hz, 1H); LCMS(electrospray) m/z 431.1 (M + H+). J 5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazole-7-carboxamide 577 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (br s, 1H), 11.14 (s, 1H), 8.60 (d, J = 6.9 Hz, 1H), 7.78 (s, 1H), 7.64 (s, 1H), 6.91 (s, 1H), 6.88 (dd, J = 1.6, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 3.23 (q, J = 6.7 Hz, 2H), 2.95 (s, 3H), 2.26 (s, 3H), 2.19-2.10 (m, 1H), 1.74- 1.61 (m, 1H), 1.21-1.14 (m, 1H), 1.07 (t, J = 7.0 Hz, 3H); LCMS(electrospray) m/z 457 (M + H+). J (1S,2S)-N-(5-(7-(ethyl(methyl)amino)-6- fluoro-5-(methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 578 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.62-12.96 (m, 1H), 11.16 (br s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.98 (s, 1H), 7.83 (s, 1H), 7.50 (d, J = 10.4 Hz, 1H), 7.04 (dd, J = 1.8, 7.1 Hz, 1H), 6.95 (s, 1H), 5.06- 4.81 (m, 1H), 3.86 (q, J = 6.9 Hz, 2H), 2.15 (td, J = 7.0, 13.6 Hz, 1H), 1.73-1.62 (m, 1H), 1.22- 1.15 (m, 1H), 1.11 (t, J = 7.0 Hz, 3H). LCMS: m/z 398.0 (M + H+) J (1S,2S)-N-(5-(5-ethoxy-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 579 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.31-11.12 (m, 1H), 8.82-8.55 (m, 1H), 8.00-7.87 (m, 1H), 7.85- 7.70 (m, 1H), 7.03-6.90 (m, 2H), 5.10-4.82 (m, 1H), 2.56-2.53 (m, 3H), 2.24-2.11 (m, 1H), 1.75- 1.61 (m, 1H), 1.26-1.13 (m, 1H); LCMS(electrospray) m/z 402.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 580 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31-12.98 (m, 1H), 11.21-11.07 (m, 1H), 8.61 (d, J = 7.0 Hz, 1H), 7.78-7.71 (m, 1H), 7.64-7.58 (m, 1H), 6.93- 6.88 (m, 2H), 6.84 (br d, J = 7.1 Hz, 1H), 5.06- 4.82 (m, 1H), 4.07 (br t, J = 5.9 Hz, 2H), 3.35- 3.27 (m, 2H), 2.98 (s, 3H), 2.53 (d, J = 4.5 Hz, 3H), 2.20 (d, J = 3.0 Hz, 3H), 2.16-2.09 (m, 1H), 1.72- 1.61 (m, 1H), 1.20-1.13 (m, 1H); LCMS(electrospray) m/z = 498.2 (M + H+). J 2-((6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 5-methyl-1H-indazol-7- yl)(methyl)amino)ethyl methylcarbamate 581 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 1.12-1.24 (m, 1 H), 1.61-1.74 (m, 1 H), 2.11-2.20 (m, 1 H), 4.82- 5.07 (m, 1 H), 6.95-6.98 (m, 1 H), 6.99 (s, 1 H) 7.50 (s, 1 H), 7.63 (s, 1 H), 7.77 (s, 1 H), 7.83 (d, J = 1.00 Hz, 1 H), 8.06 (s, 1 H), 8.71 (d, J = 7.13 Hz, 1 H), 11.20 (s, 1 H), 13.85-13.92 (m, 1 H); LCMS(electrospray) m/z 438.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-7- (difluoromethyl)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 582 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.19 (s, 1H), 8.69 (d, J = 7.1 Hz, 1H), 8.06 (s, 1H), 7.74 (s, 1H), 6.97 (s, 1H), 6.90 (dd, J = 1.8, 7.1 Hz, 1H), 5.10- 4.72 (m, 1H), 2.26 (d, J = 2.6 Hz, 3H), 2.15 (td, J = 6.6, 13.5 Hz, 1H), 1.73-1.60 (m, 1H), 1.25- 1.13 (m, 1H); LCMS(electrospray) m/z 393.1 (M + H+). J (1S,2S)-N-(5-(7-cyano-6-fluoro-5-methyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 583 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.38 (s, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.2 Hz, 1H), 8.29 (s, 1H), 7.93 (d, J = 1.0 Hz, 1H), 7.23 (d, J = 13.7 Hz, 1H), 7.16 (dd, J = 2.0, 7.2 Hz, 1H), 6.94 (s, 1H), 5.06- 4.83 (m, 1H), 2.95 (d, J = 2.0 Hz, 6H), 2.14 (br s, 1H), 1.77-1.57 (m, 1H), 1.17 (br s, 1H); LCMS(electrospray) m/z 397.2 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 584 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.31-13.17 (m, 1H), 11.26-11.08 (m, 1H), 8.66 (d, J = 7.1 Hz, 1H), 8.49-8.38 (m, 1H), 7.85-7.76 (m, 1H), 7.70 (s, 1H), 6.95 (s, 1H), 6.88 (s, 1H), 5.07-4.82 (m, 1H), 2.90 (d, J = 4.6 Hz, 3H), 2.25 (d, J = 3.1 Hz, 3H), 2.15 (td, J = 6.7, 13.8 Hz, 1H), 1.74-1.62 (m, 1H), 1.21-1.09 (m, 1H); LCMS(electrospray) m/z 425.1 (M + H+). J 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N,5-dimethyl-1H-indazole-7-carboxamide 585 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.82-13.52 (m, 1H), 11.19 (s, 1H), 8.69 (d, J = 7.0 Hz, 1H), 7.91 (s, 1H), 7.70 (d, J = 0.9 Hz, 1H), 6.96 (s, 1H), 6.86 (dd, J = 1.9, 7.1 Hz, 1H), 5.06-4.83 (m, 1H), 2.68-2.63 (m, 2H), 2.19-2.10 (m, 1H), 1.74-1.62 (m, 1H), 1.20-1.14 (m, 1H), 1.10 (t, J = 7.5 Hz, 3H); LCMS(electrospray) m/z 450.2 (M + H+). J (1S,2S)-N-(5-(5-ethyl-6-fluoro-7- (trifluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 586 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.21 (s, 1H), 8.73 (d, J = 7.2 Hz, 1H), 8.24 (s, 1H), 7.86 (s, 1H), 7.02 (s, 1H), 6.97 (dd, J = 1.9, 7.2 Hz, 1H), 5.10- 4.78 (m, 1H), 2.22-2.10 (m, 1H), 1.76-1.58 (m, 1H), 1.22-1.15 (m, 1H); LCMS(electrospray) m/z 413.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-7-cyano-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 587 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.11 (s, 1H), 11.17 (s, 1H), 8.68-8.66 (m, 1H), 8.45(s, 1H), 8.04 (s, 1H), 7.52 (d, J = 11.2 Hz, 1H), 7.22-7.21 (m, 1H), 6.99 (s, 1H), 5.02-4.86 (m, 1H), 2.15 (br s, 1H), 1.72-1.70 (m, 1 H) 1.19-1.18 (m, 1 H); LCMS(electrospray) m/z 438.2 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 588 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.84-13.52 (m, 1H), 11.32-11.10 (m, 1H), 8.75-8.60 (m, 1H), 7.97-7.76 (m, 1H), 7.72-7.64 (m, 1H), 6.99-6.91 (m, 1H), 6.89-6.80 (m, 1H), 5.09-4.81 (m, 1H), 4.26-4.07 (m, 2H), 2.75-2.62 (m, 2H), 2.24-2.10 (m, 1H), 1.77-1.62 (m, 1H), 1.23-1.15 (m, 1H), 1.15-1.09 (m, 3H); LCMS(electrospray) m/z 453.1 (M + H+). J (1S,2S)-N-(5-(7-((cyanomethyl)thio)-5- ethyl-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 589 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64 (s, 1 H) 11.17 (s, 1 H) 8.65 (d, J = 7.2 Hz, 1 H) 8.38 (s, 1 H) 8.02 (s, 1 H) 7.37 (d, J = 8.8 Hz, 1 H) 7.22-7.19 (m, 1 H) 6.98 (s, 1 H), 5.05-4.84 (m, 1 H) 2.52 (s, 3 H) 2.16-2.13 (m, 1H) 1.72-1.64 (m, 1H) 1.20- 1.15 (m, 1 H); LCMS(electrospray) m/z 400.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-7- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 590 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.74 (br s, 1H), 8.24 (d, J = 8.3 Hz, 1H), 7.79 (s, 1H), 7.76 (d, J = 11.9 Hz, 1H), 7.66 (d, J = 8.3 Hz, 1H), 5.19-4.94 (m, 1H), 2.26 (td, J = 6.9, 13.6 Hz, 1H), 1.84-1.70 (m, 1H), 1.39-1.27 (m, 1H); LCMS(electrospray) m/z 440.2 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5- (trifluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 591 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (s, 1H), 11.18 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.89 (d, J = 0.7 Hz, 1H), 7.72-7.41 (m, 2H), 6.95 (s, 1H), 6.89 (dd, J = 1.8, 7.0 Hz, 1H), 5.09-4.81 (m, 1H), 2.24 (d, J = 2.6 Hz, 3H), 2.19-2.11 (m, 1H), 1.76-1.60 (m, 1H), 1.25-1.11 (m, 1H); LCMS(electrospray) m/z 418.1 (M + H+). J (1S,2S)-N-(5-(7-(difluoromethyl)-6- fluoro-5-methyl-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 592 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.95 (s, 1H), 11.18 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.94 (s, 1H), 7.72 (s, 1H), 6.95 (s, 1H), 6.90 (dd, J = 1.8, 7.1 Hz, 1H), 5.11-4.78 (m, 1H), 2.28 (d, J = 2.8 Hz, 3H), 2.20-2.10 (m, 1H), 1.74-1.61 (m, 1H), 1.24-1.12 (m, 1H); LCMS(electrospray) m/z 452.2 (M + H+). J (1S,2S)-2-fluoro-N-(5-(6-fluoro-5-methyl- 7-(trifluoromethoxy)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 593 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.43-13.58 (m, 1 H) 11.13 (s, 1 H) 8.62 (d, J = 7.13 Hz, 1 H) 8.36 (s, 1 H) 7.94 (d, J = 1.25 Hz, 1 H) 7.36 (s, 2 H) 7.17 (dd, J = 7.25, 2.00 Hz, 1 H) 6.95 (s, 1 H) 4.80- 5.07 (m, 1 H) 2.63 (s, 3 H) 2.10-2.18 (m, 1 H) 1.62-1.73 (m, 1 H) 1.17 (ddt, J = 12.32, 9.04, 6.27, 6.27 Hz, 1 H); LCMS(electrospray) m/z = 382.1 (M + H+). J (1S,2S)-2-fluoro-N-(5-(7-(methylthio)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)cyclopropane-1-carboxamide 594 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.69 (s, 1H), 11.14 (s, 1H), 8.93 (s, 1H), 8.26-8.23 (m, 2H), 7.65 (d, J = 9.3 Hz, 1H), 7.51-7.39 (m, 1H), 5.11-4.77 (m, 1H), 4.13 (s, 3H), 2.18 (td, J = 6.8, 13.8 Hz, 1H), 1.81-1.59 (m, 1H), 1.27-1.11 (m, 1H); LCMS(electrospray) m/z 470.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1- methyl-1H-tetrazol-5-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 595 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26 (br s, 1H), 11.11 (s, 1H), 8.57 (br d, J = 7.1 Hz, 1H), 8.28 (s, 1H), 7.84 (s, 1H), 7.26 (br d, J = 7.7 Hz, 1H), 7.13 (dd, J = 2.0, 7.3 Hz, 1H), 6.90 (s, 1H), 6.80 (br d, J = 7.7 Hz, 1H), 5.08-4.79 (m, 1H), 2.93 (s, 6H), 2.14 (quin, J = 6.9 Hz, 1H), 1.74-1.60 (m, 1H), 1.17 (tdd, J = 6.2, 9.0, 12.3 Hz, 1H); LCMS(electrospray) m/z 379.1 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 596 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63 (s, 1H), 11.19 (s, 1H), 8.63 (d, J = 7.2 Hz, 1H), 8.45 (br, 1H), 7.97 (s, 1H), 7.84 (s, 1H), 6.99 (s, 1H), 6.85 (d, J = 7.2 Hz, 1H), 5.04-4.85 (m, 1H), 3.53 (s, 3H), 2.16-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.28- 1.12 (m, 1H); LCMS (electrospray) m/z 495.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl(pyrimidin-2-yl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 597 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67 (s, 1H), 11.19 (s, 1H), 8.67 (d, J = 7.2 Hz, 1H), 7.82 (s, 1H), 7.69 (s, 1H), 6.94 (s, 1H), 6.85 (d, J = 7.2 Hz, 1H), 5.04-4.87 (m, 1H), 4.50 (q, J = 7.2 Hz, 1H), 2.69- 2.60 (m, 2H), 4.23 (s, 2H), 2.16-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.60 (d, J = 12 Hz, 3H), 1.28- 1.11 (m, 4H); LCMS (electrospray) m/z 467.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- ((cyanomethyl)thio)-6-fluoro-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 598 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.15 (s, 1H), 11.17 (s, 1H), 8.63 (d, J = 7.6 Hz, 1H), 7.96 (s, 1H), 7.67 (s, 1H), 6.94 (s, 1H), 6.88 (d, J = 7.2 Hz, 1H), 5.04-4.87 (m, 1H), 2.30 (s, 3H), 2.15-2.13 (m, 1H), 1.71-1.64 (m, 1H), 1.24-1.18 (m, 1H); LCMS (electrospray) m/z 418.10 (M + H)+. J (1R,2R)-N-(5-(6,7-difluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 599 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.13 (s, 1H), 11.29 (s, 1H), 8.64 (d, J = 6.0 Hz, 1H), 7.96 (s, 1H), 7.66 (s, 1H), 6.90-6.88 (m, 2H), 5.00-4.84 (m, 1H), 2.50-2.43 (m, 1H), 2.30 (s, 3H), 1.58-1.49 (m, 1H), 1.30-1.24 (m, 1H); LCMS (electrospray) m/z 418.10 (M + H)+. J (1S,2R)-N-(5-(6,7-difluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 600 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.11 (s, 1H), 11.29 (s, 1H), 8.64 (d, J = 7.2 Hz, 1H), 7.96 (s, 1H), 7.66 (s, 1H), 6.90-6.88 (m, 2H), 5.00-4.84 (m, 1H), 2.50- 2.43 (m, 1H), 2.30 (s, 3H), 1.57 (m, 1H), 1.29-1.24 (m, 1H); LCMS (electrospray) m/z 418.10 (M + H)+. J (1R,2S)-N-(5-(6,7-difluoro-5- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 601 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.39 (s, 1H), 11.19 (s, 1H), 9.49 (s, 1H), 8.69 (d, J = 7.2 Hz, 1 H), 8.42 (d, J = 4.4 Hz, 1H), 7.91 (s, 1H), 7.83- 7.82 (m, 1H), 6.99-6.97 (m, 1H), 6.86 (t, J = 5.0 Hz, 1H), 5.05-4.85 (m, 1H), 2.17-2.13 (m, 1H), 1.71-1.63 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 481.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (pyrimidin-2-ylamino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 602 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63 (s, 1H), 11.21 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.05 (s, 1H), 7.85 (s, 1H), 7.00 (s, 1H), 6.98 (d, J = 7.2 Hz, 1H), 5.04-4.87 (m, 1H), 4.23 (s, 2H), 2.16-2.12 (m, 1H), 1.70-1.63 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 459.1 (M + H)+. J (1S,2S)-N-(5-(7-((1-cyanoethyl)thio)-5- ethyl-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 603 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.65 (s, 1H), 11.19 (s, 1H), 8.67 (d, J = 7.2 Hz, 1H), 7.81 (s, 1H), 7.71 (s, 1H), 6.94 (s, 1H), 6.87 (d, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 2.66-2.63 (m, 2H), 2.18- 2.11 (m, 1H), 1.73 (s, 6H), 1.70-1.62 (m, 1H), 1.28-1.12 (m, 1H), 1.12 (t, J = 5.2 Hz, 3H); LCMS (electrospray) m/z 481.1 (M + H)+. J (1S,2S)-N-(5-(7-((2-cyanopropan-2- yl)thio)-5-ethyl-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 604 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.93-13.02 (m, 1H), 11.17 (s, 1H), 8.63 (d, J = 7.2 Hz, 1H), 8.05 (s, 1H), 7.69 (d, J = 1.0 Hz, 1H), 7.52 (dd, J = 0.8, 9.5 Hz, 1H), 6.96 (s, 1H), 6.89 (td, J = 2.2, 7.2 Hz, 1H), 5.14-4.72 (m, 1H), 2.85 (s, 3H), 2.72 (d, J = 1.6 Hz, 3H), 2.14 (td, J = 6.9, 13.8 Hz, 1H), 1.75-1.59 (m, 1H), 1.17 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 425.2 (M + H+). J 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N,N-dimethyl-1H-indazole-7-carboxamide 605 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.93-13.02 (m, 1H), 11.17 (s, 1H), 8.63 (d, J = 7.2 Hz, 1H), 8.05 (s, 1H), 7.69 (d, J = 1.0 Hz, 1H), 7.52 (dd, J = 0.8, 9.5 Hz, 1H), 6.96 (s, 1H), 6.89 (td, J = 2.2, 7.2 Hz, 1H), 5.14-4.72 (m, 1H), 2.85 (s, 3H), 2.72 (d, J = 1.6 Hz, 3H), 2.14 (td, J = 6.9, 13.8 Hz, 1H), 1.75-1.59 (m, 1H), 1.17 (tdd, J = 6.2, 9.1, 12.3 Hz, 1H); LCMS(electrospray) m/z 425.2 (M + H+ J 6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N,N-dimethyl-1H-indazole-5-carboxamide 606 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.16 (s, 1H), 8.64 (br d, J = 7.1 Hz, 1H), 8.06 (s, 1H), 7.83 (s, 1H), 7.03 (br dd, J = 1.8, 7.1 Hz, 1H), 6.96 (s, 1H), 5.06-4.82 (m, 1H), 3.86 (br d, J = 7.0 Hz, 2H), 2.55 (s, 3H), 2.18-2.12 (m, 1H), 1.73-1.61 (m, 1H), 1.26-1.15 (m, 1H), 1.11 (br t, J = 6.9 Hz, 3H); LCMS(electrospray) m/z 444.2 (M + H+). J (1S,2S)-N-(5-(5-ethoxy-6-fluoro-7- (methylthio)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 607 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.06-13.49 (m, 1H), 10.62 (br s, 1H), 9.03 (d, J = 7.0 Hz, 1H), 8.56 (s, 1H), 8.25 (s, 1H), 7.58 (s, 1H), 7.44 (dd, J = 1.8, 7.1 Hz, 1H), 5.46-5.25 (m, 1H), 2.69 (br s, 1H), 2.27- 2.21 (m, 1H), 1.69-1.61 (m, 1H); LCMS(electrospray) m/z 472.0 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (trifluoromethoxy)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 608 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.64 (s, 1H), 11.19 (s, 1H), 8.67 (d, J = 7.2 Hz, 1H), 7.82 (s, 1H), 7.71 (s, 1H), 6.94 (s, 1H), 6.88 (d, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 2.66-2.63 (m, 2H), 2.18- 2.11 (m, 1H), 1.73-7.72 (m, 2H), 1.70-1.62 (m, 1H), 1.62-1.60 (m, 1H), 1.28-1.12 (m, 1H), 1.12 (t, J = 5.2 Hz, 3H); LCMS (electrospray) m/z 479.1 (M + H)+. J (1S,2S)-N-(5-(7-((1- cyanocyclopropyl)thio)-5-ethyl-6-fluoro- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 609 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63 (s, 1H), 11.20 (s, 1H), 8.99 (s, 1H), 8.69 (d, J = 7.2 Hz, 1H), 8.21 (d, J = 6.4 Hz, 2H), 7.99 (s, 1H), 7.83-7.82 (m, 1H), 7.01-6.98 (m, 2H), 6.62 (d, J = 4.8 Hz, 2H), 5.04-4.85 (m, 1H), 2.17-2.12 (m, 1H), 1.71- 1.63 (m, 1H), 1.21-1.16 (m, 1H); LCMS (electrospray) m/z 480.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (pyridin-4-ylamino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 610 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.28 (br s, 1H), 11.15 (s, 1H), 8.60 (d, J = 7.0 Hz, 1H), 7.96 (s, 1H), 7.77 (s, 1H), 7.01 (dd, J = 1.8, 7.3 Hz, 1H), 6.92 (s, 1H), 5.04-4.83 (m, 1H), 3.83 (q, J = 7.0 Hz, 2H), 2.98 (br s, 6H), 2.18-2.11 (m, 1H), 1.72-1.6 (m, 1H), 1.18 (br s, 1H), 1.11 (t, J = 7.0 Hz, 3H); LCMS(electrospray) m/z 441.1 (M + H+). J (1S,2S)-N-(5-(7-(dimethylamino)-5- ethoxy-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 611 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.96 (s, 1H), 11.17 (s, 1H), 8.64 (d, J = 7.2 Hz, 1H), 8.18-8.12 (m, 1H), 7.81 (s, 1H), 7.02-6.93 (m, 2H), 5.04- 4.84 (m, 1H), 3.96-3.82 (m, 2H), 2.18-2.09 (m, 1H), 1.70-1.60 (m, 1H), 1.20-1.16 (m, 1H), 1.12 (t, J = 6.8 Hz, 3H); LCMS(electrospray) m/z 416.1 (M + H+). J (1S,2S)-N-(5-(5-ethoxy-6,7-difluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 612 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.85 (s, 1H), 11.22 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.01 (s, 1H), 7.82 (s, 1H), 6.99 (s, 1H), 6.97 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 4.72 (s, 2H), 3.03 (s, 3H), 2.18-2.11 (m, 1H), 1.70-1.62 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. J 5-chloro-N-(cyanomethyl)-6-fluoro-4-(2- ((1S,2S)-2-fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- N-methyl-1H-indazole-7-carboxamide 613 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.62 (s, 1H), 11.21 (s, 1H), 8.70 (d, J = 7.2 Hz, 1H), 8.55 (s, 1H), 7.98 (s, 1H), 7.84 (s, 1H), 7.00-6.99 (m, 2H), 5.03- 4.86 (m, 1H), 3.52 (s, 3H), 2.17-2.12 (m, 1H), 1.71-1.64 (m, 1H), 1.21-1.14 (m, 1H); LCMS (electrospray) m/z 513.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((5- fluoropyrimidin-2-yl)(methyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 614 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.75 (s, 1H), 11.20 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.22 (d, J = 6.8 Hz, 1H), 8.04 (s, 1H), 7.84 (s, 1H), 7.01 (dd, J = 2.2, 7.0 Hz, 2H), 6.60 (d, J = 5.6 Hz, 1H), 5.06- 4.86 (m, 1H), 3.41 (s, 3H), 2.19-2.12 (m, 1H), 1.73-1.63 (m, 1H), 1.21-1.17 (m, 1H); LCMS (electrospray) m/z 494.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl(pyridin-4-yl)amino)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 615 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.02 (s, 1H), 11.21 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.09 (s, 1H), 7.83 (s, 1H), 7.00 (s, 1H), 6.97 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 4.79 (dd, J = 18 Hz, 110 Hz, 2H), 2.18-2.11 (m, 1H), 1.90 (s, 3H), 1.70-1.62 (m, 1H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 484.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(N- (cyanomethyl)acetamido)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 616 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 11.19 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 8.38 (dd, J = 1.6, 4.4 Hz, 2H), 7.89 (s, 1H), 7.73-7.72 (m, 1H), 7.21 (d, J = 6.0 Hz, 2H), 6.95 (s, 1H), 6.90 (dd, J = 2.4, 7.2 Hz, 1H), 5.05-4.84 (m, 1H), 3.54 (t, 2H), 3.06 (d, J = 2.0 Hz, 3H), 2.86 (t, J = 7.4 Hz, 2H), 2.18-2.11 (m, 1H), 1.72-1.64 (m, 1H), 1.21- 1.13 (m, 1H); LCMS (electrospray) m/z 522.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl(2-(pyridin-4-yl)ethyl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 617 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.70 (s, 1H), 11.21 (s, 1H), 8.91 (d, J = 0.8 Hz, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.58 (d, J = 2.0 Hz, 1H), 8.01 (s, 1H), 7.85 (s, 1H), 7.01-6.99 (m, 2H), 5.04-4.85 (m, 1H), 3.55 (s, 3H), 2.18-2.11 (m, 1H), 1.71-1.64 (m, 1H), 1.21-1.14 (m, 1H); LCMS (electrospray) m/z 496.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl(1,3,5-triazin-2-yl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 618 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67 (s, 1H), 11.21 (s, 1H), 8.88 (d, J = 2.0 Hz, 1H), 8.71 (d, J = 7.2 Hz, 1H), 8.38 (s, 1H), 8.01 (s, 1H), 7.85 (s, 1H), 7.01-6.99 (m, 2H), 5.05-4.84 (m, 1H), 3.63 (s, 3H), 2.18-2.11 (m, 1H), 1.71-1.63 (m, 1H), 1.21- 1.11 (m, 1H); LCMS (electrospray) m/z 496.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (methyl(1,2,4-triazin-3-yl)amino)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 619 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.29 (s, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.3 Hz, 1H), 7.87 (s, 1H), 7.71 (s, 1H), 6.92-6.90 (m, 2H), 5.18-5.17 (m, 1H), 5.03-4.85 (m, 1H), 4.03 (s, 1H), 2.17-2.09 (m, 1H), 1.72-1.62 (m, 1H), 1.23 (d, J = 6.4 Hz, 6H), 1.20-1.15 (m, 1H); LCMS (electrospray) m/z 445.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (isopropylamino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 620 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 11.19 (s, 1H), 8.65 (d, J = 7.2 Hz, 1H), 7.88 (s, 1H), 7.76 (s, 1H), 6.94 (s, 1H), 6.92 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 3.93 (t, J = 9.6 Hz, 1H), 2.84 (s, 3H), 2.18-2.07 (m, 3H), 1.96-1.86 (m, 2H), 1.72-1.57 (m, 3H), 1.28-1.12 (m, 1H); LCMS (electrospray) m/z 471.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- (cyclobutyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 621 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.81 (s, 1H), 11.21 (s, 1H), 8.69 (d, J = 7.2 Hz, 1H), 7.88 (s, 1H), 7.81 (s, 1H), 6.97 (s, 1H), 6.95 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 3.02 (q, J = 7.3 Hz, 2H), 2.18- 2.08 (m, 1H), 1.72-1.62 (m, 1H), 1.22-1.13 (m, 4H); LCMS (electrospray) m/z 448.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(ethylthio)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 622 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (s, 1H), 11.20 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.89 (s, 1H), 7.76 (d, J = 1.2 Hz, 1H), 6.95-6.93 (m, 2H), 5.03- 4.84 (m, 1H), 3.56 (s, 1H), 2.89 (d, J = 3.6 Hz, 3H), 2.18-2.11 (m, 1H), 1.72-1.62 (m, 1H), 1.22- 1.15 (m, 7H); LCMS (electrospray) m/z 459.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (isopropyl(methyl)amino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 623 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.66 (s, 1H), 11.21 (s, 1H), 8.70 (d, J = 7.2 Hz, 1H), 7.97 (s, 1H), 7.80 (m, 1H), 6.97-6.94 (m, 2H), 5.05-4.85 (m, 1H), 3.84 (t, J = 7.8 Hz, 2H), 3.60 (t, J = 8.0 Hz, 2H), 2.82 (s, 3H), 2.18-2.11 (m, 1H), 1.73-1.62 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 486.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- methyl-2-oxoimidazolidin-1-yl)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 624 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.13 (s, 1H), 11.17 (s, 1H), 8.62 (d, J = 6.8 Hz, 1H), 7.86 (s, 1H), 7.69 (d, J = 0.8 Hz, 1H), 6.96-6.86 (m, 2H), 5.05- 4.83 (m, 1H), 4.68-4.58 (m, 2H), 4.37-4.30 (m, 1H), 4.27-4.16 (m, 2H), 3.27 (s, 3H), 2.18-2.09 (m, 1H), 1.73-1.61 (m, 1H), 1.20-1.12 (m, 1H); LCMS (electrospray) m/z 473.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- methoxyazetidin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 625 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 11.19 (s, 1H), 8.65 (d, J = 7.2 Hz, 1H), 7.87 (s, 1H), 7.76 (s, 1H), 6.94 (s, 1H), 6.92 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 3.01-2.98 (m, 4H), 2.18-2.08 (m, 1H), 1.72-1.62 (m, 1H), 1.22-1.13 (m, 4H), 0.63-0.60 (m, 2H), 0.49-0.45 (m, 2H); LCMS (electrospray) m/z 457.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- (cyclopropyl(methyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 626 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.02 (s, 1H), 11.24 (s, 1H), 10.49 (s, 1H), 8.73 (d, J = 7.2 Hz, 1H), 8.07 (s, 1H), 7.89-7.87 (m, 1H), 7.02 (s, 1H), 7.00 (dd, J = 7.0, 1.8 Hz, 1H), 5.06-4.85 (m, 1H), 2.19-2.12 (m, 1H), 1.73-1.63 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 416.05 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-formyl- 1H-indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)-2-fluorocyclopropane-1-carboxamide 627 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.06 (s, 1H), 11.13 (s, 1H), 8.58 (d, J = 6.8 Hz, 1H), 7.81 (s, 1H), 7.64 (s, 1H), 6.90-6.81 (m, 2H), 5.02-4.80 (m, 1H), 4.49-4.40 (m, 2H), 4.20-4.04 (m, 2H), 3.53 (d, J = 6.4 Hz, 2H), 3.25 (s, 3H), 2.99-2.88 (m, 1H), 2.15-2.04 (m, 1H), 1.68-1.57 (m, 1H), 1.17- 1.09 (m, 1H); LCMS (electrospray) m/z 487.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- (methoxymethyl)azetidin-1-yl)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 628 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.62 (s, 1H), 11.20 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 7.95 (d, J = 2.0 Hz, 1H), 7.74 (d, J = 1.2 Hz, 1H), 6.96 (s, 1H), 6.91 (dd, J = 1.6, 7.2 Hz, 1H), 5.06-4.84 (m, 1H), 3.69-3.61 (m, 4H), 3.47-3.39 (m, 4H), 2.18-2.10 (m, 1H), 1.73-1.61 (m, 1H), 1.21-1.12 (m, 1H); LCMS (electrospray) m/z 521.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(1,1- dioxidothiomorpholino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 629 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.57 (s, 1H), 11.20 (s, 1H), 10.49 (s, 1H), 8.68 (d, J = 7.2 Hz, 1H), 8.07 (s, 1H), 7.89-7.87 (m, 1H), 7.02 (s, 1H), 7.00 (dd, J = 7.0, 1.8 Hz, 1H), 5.06-4.85 (m, 1H), 2.19-2.12 (m, 1H), 1.73-1.63 (m, 1H), 1.21-1.15 (m, 1H); LCMS (electrospray) m/z 416.05 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (hydroxymethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 630 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 11.19 (s, 1H), 8.61 (d, J = 7.2 Hz, 1H), 7.91 (s, 1H), 7.76 (s, 1H), 6.94 (s, 1H), 6.87 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 4.55-4.51 (m, 2H), 3.98-3.94 (m, 2H), 2.85-2.80 (m, 1H), 2.15-2.08 (m, 1H), 1.72-1.62 (m, 1H), 1.29-1.12 (m, 4H), 0.86-0.79 (m, 1H); LCMS (electrospray) m/z 457.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- methylazetidin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 631 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.49 (s, 1H), 11.19 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.91 (s, 1H), 7.74 (t, J = 1.2 Hz, 1H), 6.95 (s, 1H), 6.91 (dd, J = 2.4, 7.2 Hz, 1H), 5.06-4.84 (m, 1H), 3.53-3.39 (m, 4H), 2.90-2.82 (m, 4H), 2.19-2.09 (m, 1H), 1.73-1.61 (m, 1H), 1.21-1.12 (m, 1H); LCMS (electrospray) m/z 489.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- thiomorpholino-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 632 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.41 (s, 1H), 11.20 (s, 1H), 8.61 (d, J = 7.2 Hz, 1H), 7.96 (s, 1H), 7.68 (s, 1H), 6.92 (s, 1H), 6.87 (s, J = 7.2 Hz, 1H), 5.04-4.84 (m, 1H), 4.55-4.44 (m, 4H), 2.15-2.08 (m, 1H), 1.72-1.62 (m, 1H), 1.66 (d, J = 22 Hz, 1H), 1.29-1.12 (m, 1H); LCMS (electrospray) m/z 475.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- fluoro-3-methylazetidin-1-yl)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 633 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.90 (br s, 1H), 11.23 (s, 1H), 8.71 (d, J = 7.2 Hz, 1H), 7.99 (d, J = 17.2 Hz, 1H), 7.85-7.83 (m, 1H), 7.00 (s, 1H), 6.97 (dd, J = 7.0, 2.0 Hz, 1H), 5.06-4.85 (m, 1H), 2.18- 2.11 (m, 1H), 1.73-1.63 (m, 1H), 1.21-1.14 (m, 1H); LCMS (electrospray) m/z 439.05 (M + H+). J (1S,2S)-N-(5-(5-chloro-7-((E)-2- cyanovinyl)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 634 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.91 (s, 1H), 11.22 (s, 1H), 8.70 (d, J = 7.2 Hz, 1H), 7.99 (s, 1H), 7.83-7.80 (m, 1H), 6.98 (s, 1H), 6.96 (dd, J = 7.0, 1.8 Hz, 1H), 5.93 (s, 1H), 5.81 (s, 1H), 5.05-4.84 (m, 1H), 2.18-2.11 (m, 1H), 1.72-1.62 (m, 1H), 1.20-1.13 (m, 1H); LCMS (electrospray) m/z 420.00 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- (fluoromethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 635 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.59 (s, 1H), 11.18 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.93 (s, 1H), 7.75 (t, J = 1.4 Hz, 1H), 6.96 (s, 1H), 6.92 (dd, J = 7.1, 1.6 Hz, 1H), 5.08-4.80 (m, 1H), 3.89 (t, J = 11.5 Hz, 2H), 3.32-3.24 (m, 2H), 3.24-3.10 (m, 2H), 2.97 (d, J = 11.5 Hz, 2H), 2.22-2.09 (m, 1H), 1.77-1.61 (m, 1H), 1.22-1.11 (m, 1H); LCMS (electrospray) m/z 505.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1- oxidothiomorpholino)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 636 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.44 (s, 1H), 11.18 (s, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.75 (s, 1H), 7.03-6.84 (m, 2H), 6.42 (s, 1H), 5.10-4.83 (m, 1H), 4.83-4.49 (m, 2H), 2.24-2.04 (m, 1H), 1.76-1.59 (m, 1H), 1.21-1.05 (m, 1H); LCMS (electrospray) m/z 442.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- ((cyanomethyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 637 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.63-14.10 (1H), 11.21 (s, 1H), 8.71 (d, J = 7.1 Hz, 1H), 8.09 (s, 1H), 7.82 (t, J = 1.4 Hz, 1H), 7.28 (s, 2H), 6.99- 6.96 (m, 2H), 6.41 (t, J = 2.2 Hz, 2H), 5.06-4.85 (m, 1H), 2.19-2.12 (m, 1H), 1.73-1.63 (m, 1H), 1.21-1.14 (m, 1H); LCMS (electrospray) m/z 453.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1H- pyrrol-1-yl)-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 638 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 11.20 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.92 (s, 1H), 7.80 (d, J = 1.1 Hz, 1H), 7.02-6.87 (m, 2H), 5.76 (s, 1H), 5.09-4.81 (m, 1H), 2.23-2.07 (m, 1H), 1.75-1.61 (m, 7H), 1.21-1.10 (m, 2H); LCMS (electrospray) m/z 470.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-((2- cyanopropan-2-yl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 639 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.67-13.30 (m, 1H), 11.18 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.94 (s, 1H), 7.79 (d, J = 1.0 Hz, 1H), 7.05-6.79 (m, 2H), 5.63 (s, 1H), 5.38 (s, 1H), 5.15-4.77 (m, 1H), 2.21 (s, 3H), 2.18-2.09 (m, 1H), 1.74-1.60 (m, 1H), 1.25-1.12 (m, 1H); LCMS (electrospray) m/z 428.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(prop- 1-en-2-yl)-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 640 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.61 (br d, J = 2.1 Hz, 1H), 11.18 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.92 (s, 1H), 7.76 (d, J = 0.9 Hz, 1H), 7.07-6.84 (m, 2H), 5.10-4.76 (m, 1H), 3.62 (td, J = 7.0, 14.1 Hz, 1H), 2.15 (td, J = 6.9, 13.8 Hz, 1H), 1.76-1.59 (m, 1H), 1.44 (d, J = 7.0 Hz, 6H), 1.18 (tdd, J = 6.2, 9.0, 12.3 Hz, 1H); LCMS (electrospray) m/z 430.2 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- isopropyl-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 641 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.32 (s, 1H), 11.03 (s, 1H), 8.61 (d, J = 7.1 Hz, 1H), 7.95 (s, 1H), 7.73 (s, 1H), 6.98-6.88 (m, 2H), 6.24-5.96 (m, 1H), 5.05-4.81 (m, 1H), 3.34-3.24 (m, 1H), 2.22-2.09 (m, 1H), 1.78-1.58 (m, 4H), 1.22-1.11 (m, 1H); LCMS (electrospray) m/z 456.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-((1- cyanoethyl)amino)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 642 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.11 (s, 1H), 10.83 (s, 1H), 8.54 (d, J = 7.1 Hz, 1H), 7.90-7.72 (m, 1H), 7.62 (s, 1H), 6.88 (s, 1H), 6.86-6.79 (m, 1H), 5.56-5.24 (m, 1H), 5.00-4.74 (m, 1H), 4.34- 3.50 (m, 4H), 2.38-2.03 (m, 3H), 1.75-1.56 (m, 1H), 1.19-1.04 (m, 1H); LCMS (electrospray) m/z 475.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(3- fluoropyrrolidin-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 643 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.83 (s, 1H), 11.08 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.99 (s, 1H), 7.82 (d, J = 5.5 Hz, 1H), 7.67-6.83 (m, 7H), 5.59- 5.07 (m, 3H), 5.05-4.79 (m, 1H), 2.23-2.09 (m, 1H), 1.79-1.62 (m, 2H), 1.43 (d, J = 7.1 Hz, 2H), 1.23-1.09 (m, 1H); LCMS (electrospray) m/z 591.20 (M + H)+. J benzyl (5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7-yl)(1-cyanoethyl)carbamate 644 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.21 (s, 1H), 8.72 (d, J = 7.2 Hz, 1H), 8.07 (s, 1H), 7.87 (d, J = 1.0 Hz, 1H), 7.05-6.99 (m, 2H), 6.95 (br s, 1H), 6.27 (t, J = 3.2 Hz, 1H), 6.16-6.11 (m, 1H), 5.08-4.84 (m, 1H), 2.16 (td, J = 6.8, 14.1 Hz, 1H), 2.10-2.04 (m, 3H), 1.78-1.63 (m, 1H), 1.23-1.15 (m, 1H); LCMS (electrospray) m/z 467.1 (M + H+). J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(2- methyl-1H-pyrrol-1-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 645 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.95-13.76 (m, 1H), 10.54 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 8.47 (s, 1H), 7.98 (s, 1H), 7.76 (d, J = 1.0 Hz, 1H), 6.91 (dd, J = 2.0, 7.1 Hz, 1H), 6.76 (s, 1H), 4.92- 4.85 (m, 1H), 4.03-3.91 (m, 2H), 3.76 (dd, J = 1.3, 10.6 Hz, 1H), 2.57 (s, 3H), 2.38-2.29 (m, 1H), 1.06 (d, J = 7.2 Hz, 3H); LCMS (electrospray) m/z 476.1(M + H+). J (3S,4R)-4-methyltetrahydrofuran-3-yl (5- (5-chloro-6-fluoro-7-(methylthio)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2- yl)carbamate 646 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.51 (s, 1H), 11.07 (s, 1H), 9.60-9.58 (m, 1H), 8.64 (d, J = 7.1 Hz, 1H), 7.87 (s, 1H), 7.72 (s, 1H), 7.53 (s, 1H), 7.28 (s, 1H), 6.94 (s, 1H), 6.90 (dd, J = 7.1, 1.8 Hz, 1H), 3.80 (s, 3H), 2.99 (7H), 2.32 (dd, J = 9.1, 4.3 Hz, 2H), 2.00-1.95 (m, 1H), 1.68-1.55 (m, 1H), 1.37-1.18 (m, 2H), 0.97 (d J = 6.2 Hz 3H). LCMS (electrospray) m/z 507.1 (M + H)+. J (1S,2R,3S)-N-(5-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2-methyl- 3-(1-methyl-1H-pyrazol-4- yl)cyclopropane-1-carboxamide 647 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.52 (s, 1H), 9.05 (s, 1H), 8.57 (d, J = 7.0 Hz, 1H), 7.87 (s, 1H), 7.65 (dd, J = 1.77, 0.79 Hz, 1H), 6.85-6.81 (m, 2H), 6.72 (s, 1H), 3.01 (s, 6H), 2.62-2.58 (m, 1H), 0.69- 0.65 (m, 2H), 0.46-0.44 (m, 2H); LCMS (electrospray) m/z 428.0 (M + H)+. J 1-(5-(5-chloro-7-(dimethylamino)-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-3-cyclopropylurea 648 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.03 (s, 1H), 8.63 (d, J = 7.2 Hz, 1H), 8.55 (s, 1H), 7.87 (s, 1H), 7.71 (s, 1H), 7.53 (s, 1H), 7.26 (s, 1H), 6.97 (s, 1H), 6.90 (dd , J = 7.1, 1.8 Hz, 1H), 3.77 (s, 3H), 3.02 (d, J = 2.2 Hz, 6H), 2.22-2.14 (m, 1H), 2.09 (d, J = 4.5 Hz, 3 H), 1.63-1.54 (m, 1H), 1.26 (d, J = 6.1 Hz, 5H), 1.06 (t, J = 7.0 Hz, 2H); LCMS (electrospray) m/z 507.1 (M + H)+. J (1S,2S,3S)-N-(5-(5-chloro-7- (dimethylamino)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2-methyl- 3-(1-methyl-1H-pyrazol-4- yl)cyclopropane-1-carboxamide 649 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 11.20 (s, 1H), 8.71 (d, J = 7.1 Hz, 1H), 8.13 (s, 1H), 7.84-7.80 (m, 1H), 7.50-7.38 (m, 1H), 7.00 (s, 1H), 6.97 (dd , J = 7.19, 1.94 Hz, 1 H), 6.66 (dd, J = 2.94, 1.69 Hz, 1 H), 5.09-4.81 (m, 1H), 3.15-2.95 (m, 5H), 2.20- 2.11 (m, 1H), 1.75-1.61 (m, 1H), 1.22-1.12 (m, 1H); LCMS (electrospray) m/z 524.1 (M + H)+. J 1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7-yl)-N,N-dimethyl-1H- pyrrole-3-carboxamide 650 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.17-13.20 (m, 1H), 11.17 (s, 1H), 8.66 (d, J = 7.2 Hz, 1H), 7.94 (s, 1H), 7.76 (s, 1H), 7.00-6.89 (m, 2H), 5.10- 4.80 (m, 1H), 4.74 (br s, 1H), 2.15 (quin, J = 6.9 Hz, 1H), 1.77-1.59 (m, 1H), 1.37 (d, J = 6.0 Hz, 6H), 1.26-1.09 (m, 1H); LCMS (electrospray) m/z 446.0 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7- isopropoxy-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 651 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.55 (s, 1H), 11.19 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.90 (d, J = 1.1 Hz, 1H), 7.76 (t, J = 1.1 Hz, 1H), 6.96-6.92 (m, 2H), 5.05-4.84 (m, 1H), 3.59 (q, J = 8.6 Hz, 1H), 2.18-1.91 (m, 8H), 1.72-1.62 (m, 3H), 1.24-1.06 (m, 1H); LCMS (electrospray) m/z 456.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-cyclopentyl-6- fluoro-1H-indazol-4-yl)pyrazolo[1,5- a]pyridin-2-yl)-2-fluorocyclopropane-1- carboxamide 652 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.35 (s, 1H), 11.15 (s, 1H), 8.65 (d, J = 7.1 Hz, 1H), 7.90 (s, 1H), 7.79 (t, J = 1.4 Hz, 1H), 7.59 (s, 1H), 6.93 (dd, J = 6.3, 2.5 Hz, 2H), 5.74 (t, J = 7.4 Hz, 1H), 5.01-4.80 (m, 1H), 2.15-2.08 (m, 1H), 1.64 (dtd, J = 23.2, 6.9, 3.8 Hz, 1H), 1.17-1.10 (m, 1H); LCMS (electrospray) m/z 487.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(2,2,2- trifluoro-1-hydroxyethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 653 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.25 (br s, 1H), 11.14 (s, 1H), 8.61 (d, J = 7.2 Hz, 1H), 7.85 (br s, 1H), 7.70 (s, 1H), 6.92 (s, 1H), 6.91-6.88 (m, 1H), 5.32 (br d, J = 9.5 Hz, 1H), 5.06-4.82 (m, 1H), 2.21-2.06 (m, 1H), 1.75-1.61 (m, 1H), 1.26 (d, J = 6.4 Hz, 3H), 1.21-1.14 (m, 1H), 1.04 (br s, 1H), 0.48-0.35 (m, 2H), 0.34-0.18 (m, 2H); LCMS (electrospray) m/z 471.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-((1- cyclopropylethyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 654 0embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.26 (s, 1H), 11.15 (s, 1H), 8.61 (d, J = 7.0 Hz, 1H), 7.85 (m, 1H), 7.70 (d, J = 1.0 Hz, 1H), 6.91 (m, 2H), 5.65 (m, 1H), 4.95 (m, 1H), 3.31 (s, 2H), 2.14 (m, 1H), 1.67 (m, 1H), 1.18 (m, 1H), 1.08 (m, 1H), 0.48 (d, J = 7.1 Hz, 2H), 0.27 (m, 2H); LCMS (electrospray) m/z 457.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7- ((cyclopropylmethyl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 655 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.56 (br s, 1H), 11.17 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.91 (s, 1H), 7.78 (s, 1H), 6.96 (br d, J = 2.2 Hz, 1H), 6.95-6.91 (m, 1H), 5.07-4.82 (m, 1H), 3.85-3.74 (m, 2H), 3.67 (br s, 1H), 3.25 (s, 3H), 2.21-2.09 (m, 1H), 1.74-1.60 (m, 1H), 1.40 (br d, J = 6.1 Hz, 3H), 1.22-1.12 (m, 1H); LCMS (electrospray) m/z 460.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((R)-1- methoxypropan-2-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 656 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.56 (br s, 1H), 11.17 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.91 (s, 1H), 7.78 (d, J = 1.0 Hz, 1H), 6.96 (d, J = 2.6 Hz, 1H), 6.95-6.92 (m, 1H), 5.07-4.79 (m, 1H), 3.85-3.73 (m, 2H), 3.67 (br s, 1H), 3.25 (s, 3H), 2.15 (td, J = 6.8, 13.7 Hz, 1H), 1.73-1.61 (m, 1H), 1.40 (br d, J = 6.2 Hz, 3H), 1.18 (ddd, J = 2.8, 6.2, 12.3 Hz, 1H); LCMS (electrospray) m/z 460.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-((S)-1- methoxypropan-2-yl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 657 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 11.15 (s, 1H), 8.62 (d, J = 7.1 Hz, 1H), 8.04-7.83 (m, 1H), 7.71 (d, J = 1.0 Hz, 1H), 6.92 (s, 1H), 6.90 (dd, J = 7.1, 2.0 Hz, 1H), 6.33-5.92 (m, 1H), 5.67- 5.51 (m, 1H), 5.07-4.81 (m, 1H), 4.53-4.03 (m, 1H), 2.21-2.05 (m, 1H), 1.75-1.57 (m, 1H), 1.32 (d, J = 6.6 Hz, 3H), 1.17 (ddt, J = 12.26, 9.07, 6.16, 6.16 Hz, 1 H); LCMS (electrospray) m/z 481.0 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-((1,1- difluoropropan-2-yl)amino)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 658 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.15 (s, 1H), 11.19 (s, 1H), 8.68 (d, J = 7.1 Hz, 1H), 7.92 (s, 1H), 7.78 (d, J = 1.0 Hz, 1H), 6.98 (s, 1H), 6.94 (dd, J = 2.0, 7.1 Hz, 1H), 5.57 (dd, J = 5.4, 10.8 Hz, 1H), 5.18 (d, J = 3.4 Hz, 1H), 5.07-4.83 (m, 1H), 4.55 (dd, J = 3.7 Hz, 1H), 4.47 (dd, J = 4.6, 8.9 Hz, 1H), 3.72 (dd, J = 1.2, 9.0 Hz, 1H), 2.26 (dd, J = 5.4, 12.5 Hz, 1H), 2.20-2.02 (m, 2H), 1.76-1.62 (m, 1H), 1.28-1.12 (m, 2H); LCMS (electrospray) m/z 474.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(4- hydroxytetrahydrofuran-2-yl)-1H-indazol- 4-yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 659 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.80-13.56 (m, 1H), 11.18 (s, 1H), 8.77 (br d, J = 6.6 Hz, 1H), 8.67 (d, J = 7.1 Hz, 1H), 8.06 (s, 1H), 7.94 (s, 1H), 7.77 (d, J = 0.9 Hz, 1H), 6.96 (s, 1H), 6.93 (dd, J = 1.8, 7.2 Hz, 1H), 5.56 (br t, J = 7.2 Hz, 1H), 5.11-4.78 (m, 1H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.73-1.62 (m, 1H), 1.58 (d, J = 7.2 Hz, 3H), 1.18 (tdd, J = 6.4, 9.0, 12.4 Hz, 1H); LCMS (electrospray) m/z 459.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1- formamidoethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 660 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.73-13.44 (m, 1H), 11.17 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 8.46- 8.32 (m, 1H), 7.92 (s, 1H), 7.77 (s, 1H), 6.96 (s, 1H), 6.93 (dd, J = 2.0, 7.2 Hz, 1H), 5.46 (br t, J = 7.0 Hz, 1H), 5.09-4.77 (m, 1H), 2.20-2.07 (m, 3H), 1.78-1.61 (m, 1H), 1.55 (br d, J = 7.2 Hz, 3H), 1.27-1.07 (m, 1H), 0.95 (t, J = 7.6 Hz, 3H); LCMS (electrospray) m/z 487.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1- propionamidoethyl)-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 661 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.77-13.42 (m, 1H), 11.18 (s, 1H), 8.67 (d, J = 7.1 Hz, 1H), 8.54- 8.48 (m, 1H), 8.34 (br s, 1H), 7.91 (s, 1H), 7.77 (d, J = 0.7 Hz, 1H), 6.95 (s, 1H), 6.93 (dd, J = 2.0, 7.2 Hz, 1H), 5.45 (br t, J = 7.1 Hz, 1H), 5.05-4.83 (m, 1H), 3.08 (br t, J = 8.3 Hz, 1H), 2.19-2.01 (m, 3H), 1.99-1.83 (m, 3H), 1.75-1.61 (m, 2H), 1.55 (d, J = 7.2 Hz, 3H), 1.17 (ddd, J = 2.8, 6.1, 12.3 Hz, 1H); LCMS (electrospray) m/z 513.2 (M + H)+. J N-(1-(5-chloro-6-fluoro-4-(2-((1S,2S)-2- fluorocyclopropane-1- carboxamido)pyrazolo[1,5-a]pyridin-5-yl)- 1H-indazol-7- yl)ethyl)cyclobutanecarboxamide 662 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ14.24-12.89 (m, 1H), 11.19 (s, 1H), 10.54-9.82 (m, 1H), 8.68 (d, J = 7.0 Hz, 1H), 7.97 (s, 1H), 7.00-6.92 (m, 2H), 5.56 (q, J = 7.0 Hz, 1H), 5.07-4.81 (m, 1H), 2.21- 2.08 (m, 1H), 1.69 (d, J = 7.0 Hz, 3H), 1.66-1.60 (m, 1H), 1.26-1.09 (m, 1H); LCMS (electrospray) m/z 527.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-6-fluoro-7-(1- (2,2,2-trifluoroacetamido)ethyl)-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 663 embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ13.90-13.44 (m, 1H), 11.21-11.13 (m, 1H), 8.94-8.80 (m, 1H), 8.66 (d, J = 7.2 Hz, 1H), 8.56 (s, 1H), 7.96-7.86 (m, 1H), 7.80-7.73 (m, 1H), 6.95 (s, 1H), 6.94-6.91 (m, 1H), 5.54-5.41 (m, 1H), 4.93 (s, 1H), 2.22-2.09 (m, 1H), 1.90-1.82 (m, 3H), 1.73-1.61 (m, 1H), 1.54 (d, J = 7.0 Hz, 3H), 1.21-1.13 (m, 1H); LCMS (electrospray) m/z 473.1 (M + H)+. J (1S,2S)-N-(5-(7-(1-acetamidoethyl)-5- chloro-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 664 00embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.73 (s, 1H), 11.21 (s, 1H), 8.70 (d, J = 7.1 Hz, 1H), 7.97 (s, 1H), 7.77 (s, 1H), 7.00 (s, 1H), 6.93 (dd, J = 7.1, 2.2 Hz, 1H), 6.40 (s, 1H), 5.05-4.85 (m, 1H), 3.20 (s, 3H), 2.58 (d, J = 4.4 Hz, 3H), 2.18-2.11 (m, 1H), 1.72- 1.64 (m, 1H), 1.21-1.15 (m, 1H) m/z 474.10 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(1,3- dimethylureido)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide 665 01embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 14.06-13.53 (m, 1H), 11.18 (s, 1H), 9.82-9.45 (m, 1H), 8.67 (d, J = 7.1 Hz, 1H), 7.95 (s, 1H), 7.78 (d, J = 0.9 Hz, 1H), 6.99-6.91 (m, 2H), 6.44-6.11 (m, 1H), 5.61-5.51 (m, 1H), 5.05-4.83 (m, 1H), 2.15 (td, J = 7.0, 13.8 Hz, 1H), 1.70 (dt, J = 3.7, 6.9 Hz, 1H), 1.65 (d, J = 7.2 Hz, 3H), 1.24-1.12 (m, 1H); LCMS (electrospray) m/z 509.2 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-(1-(2,2- difluoroacetamido)ethyl)-6-fluoro-1H- indazol-4-yl)pyrazolo[1,5-a]pyridin-2-yl)- 2-fluorocyclopropane-1-carboxamide 666 02embedded image .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ 13.33 (s, 1H), 11.20 (s, 1H), 8.67 (t, J = 8.0 Hz, 1H), 7.91 (s, 1H), 7.82 (t, J = 1.1 Hz, 1H), 6.97 (dd, J = 7.1, 2.2 Hz, 2H), 5.04-4.85 (m, 2H), 3.90 (t, J = 6.3 Hz, 1H), 3.38 (d, J = 6.6 Hz, 3H), 3.25 (s, 3H), 2.14 (t, J = 8.0 Hz, 1H), 1.71-1.64 (m, 1H), 1.18 (dd, J = 12.1, 8.8 Hz, 1H), 0.95 (d, J = 6.6 Hz, 3H); LCMS (electrospray) m/z 490.1 (M + H)+. J (1S,2S)-N-(5-(5-chloro-7-((1S,2R)-1,2- dimethoxypropyl)-6-fluoro-1H-indazol-4- yl)pyrazolo[1,5-a]pyridin-2-yl)-2- fluorocyclopropane-1-carboxamide

(252) Evaluation of Compounds

(253) HPK1 Kinase Assay

(254) HPK1 kinase activity was measured by Promega's ADP-Glo™ kinase assay. In this assay, 5 ng of recombinant human HPK1 (signalchem) is incubated with 5 μL of compounds (0.5% DMSO), 5 μL of MBP (0.5 μg/μl) and 5 μL of ATP (25 μM) in buffer (40 mM Tris, 7.5; 20 mM MgCl.sub.2; 0.1 mg/ml BSA; 5 μM DTT). The assay was started by incubating the reaction mixture in a 96-well plate at 30′ C for 40 minutes. After the incubation, 25 uL ADP-Glo reagent was added and the reaction was incubated at room temperature for 40-min to stop the reaction and degrade residual ATP. The ADP product was then converted to ATP by adding 50 uL per well of detection reagent. Luminescence was detected after 30-min room temperature incubation with the Molecular device I3X plate reader. The IC.sub.50 values were calculated from a series of percent inhibition values determined at a range of inhibitor concentration using software routines as implemented in the GraphPad Prism 7 software and SigmaPlot13.0.

(255) Table 2 shows IC.sub.50 values of the invented compounds which represent + for >1000 nM, ++ for 501-1000 nM, +++ for 101-500 nM, ++++ for <100 nM.

(256) TABLE-US-00002 TABLE 2 In vitro activity against HPK1 data Example HPK1 IC.sub.50 (nM) 1 +++ 2 +++ 3 + 4 ++ 5 +++ 6 +++ 7 +++ 8 + 9 + 10 + 11 ++ 12 + 13 + 14 + 15 +++ 16 +++ 17 +++ 18 + 19 + 20 + 21 + 22 + 23 + 24 +++ 25 ++ 26 + 27 + 28 +++ 29 +++ 30 +++ 31 + 32 +++ 33 +++ 34 + 35 +++ 36 +++ 37 +++ 38 + 39 +++ 40 ++++ 41 +++ 42 +++ 43 ++++ 44 ++ 45 + 46 ++++ 47 ++++ 48 ++++ 49 ++ 50 ++++ 51 ++++ 52 + 53 +++ 54 + 55 +++ 56 ++++ 57 ++++ 58 ++++ 59 ++++ 60 + 61 ++++ 62 +++ 63 ++++ 64 ++++ 65 ++++ 66 ++++ 67 ++++ 68 ++++ 69 ++++ 70 ++++ 71 ++++ 72 +++ 73 ++++ 74 +++ 75 +++ 76 +++ 77 ++++ 78 +++ 79 ++++ 80 ++++ 81 ++++ 82 ++++ 83 +++ 84 ++++ 85 ++++ 86 ++++ 87 ++++ 88 ++++ 89 ++++ 90 ++++ 91 +++ 92 ++++ 93 ++++ 94 ++++ 95 ++++ 96 ++++ 97 ++++ 98 ++++ 99 ++++ 100 ++++ 101 ++++ 102 ++++ 103 ++++ 104 ++++ 105 ++++ 106 ++++ 107 ++++ 108 ++++ 109 ++++ 110 ++++ 111 ++++ 112 +++ 113 ++++ 114 +++ 115 ++++ 116 ++++ 117 ++++ 118 ++++ 119 +++ 120 ++++ 121 + 122 ++++ 123 ++++ 124 + 125 ++++ 126 ++++ 127 ++++ 128 +++ 129 ++++ 130 ++++ 131 +++ 132 +++ 133 ++++ 134 ++++ 135 + 136 ++++ 137 ++++ 138 ++++ 139 ++++ 140 + 141 + 142 + 143 ++++ 144 +++ 145 + 146 +++ 147 ++++ 148 + 149 ++++ 150 ++++ 151 + 152 ++++ 153 ++++ 154 ++++ 155 ++++ 156 ++++ 157 +++ 158 +++ 159 ++++ 160 ++++ 161 ++++ 162 ++++ 163 ++++ 164 + 165 ++++ 166 ++++ 167 ++++ 168 +++ 169 ++++ 170 ++++ 171 + 172 ++++ 173 ++++ 174 ++++ 175 ++++ 176 ++++ 177 +++ 178 ++++ 179 ++++ 180 +++ 181 +++ 182 + 183 ++++ 184 ++++ 185 +++ 186 ++++ 187 ++++ 188 + 189 ++++ 190 ++++ 191 ++++ 192 ++++ 193 ++++ 194 ++++ 195 +++ 196 ++++ 197 ++++ 198 ++++ 199 ++++ 200 ++++ 201 + 202 ++++ 203 ++++ 204 ++++ 205 ++++ 206 +++ 207 ++++ 208 ++++ 209 ++++ 210 ++++ 211 ++++ 212 + 213 + 214 + 215 + 216 + 217 ++++ 218 ++++ 219 +++ 220 + 221 +++ 222 ++ 223 ++++ 224 +++ 225 + 226 ++++ 227 + 228 + 229 ++++ 230 + 231 + 232 ++++ 233 ++ 234 + 235 ++++ 236 ++++ 237 ++++ 238 ++++ 239 ++++ 240 ++ 241 + 242 +++ 243 ++++ 244 +++ 245 ++++ 246 ++++ 247 ++++ 248 ++++ 249 +++ 250 ++++ 251 + 252 ++++ 253 ++++ 254 ++++ 255 ++++ 256 ++++ 257 ++++ 258 ++++ 259 + 260 ++++ 261 ++++ 262 ++++ 263 ++++ 264 ++++ 265 ++++ 266 ++++ 267 +++ 268 ++++ 269 ++++ 270 +++ 271 ++++ 272 ++++ 273 ++++ 274 ++++ 275 ++++ 276 ++++ 277 +++ 278 + 279 ++++ 280 ++++ 281 ++++ 282 ++++ 283 ++++ 284 +++ 285 ++++ 286 + 287 ++++ 288 ++++ 289 + 290 ++++ 291 ++++ 292 ++++ 293 ++++ 294 ++++ 295 ++++ 296 ++++ 297 ++++ 298 ++++ 299 +++ 300 ++++ 301 ++++ 302 +++ 303 ++++ 304 ++++ 305 ++++ 306 ++++ 307 ++++ 308 +++ 309 ++++ 310 ++++ 311 ++++ 312 ++++ 313 + 314 + 315 ++++ 316 ++++ 317 ++++ 318 ++++ 319 ++++ 320 ++++ 321 ++++ 322 +++ 323 ++++ 324 ++++ 325 + 326 ++++ 327 ++++ 328 ++++ 329 ++++ 330 ++++ 331 ++++ 332 ++++ 333 ++++ 334 ++++ 335 ++++ 336 ++++ 337 ++++ 338 +++ 339 ++++ 340 +++ 341 ++++ 342 ++++ 343 ++++ 344 +++ 345 ++++ 346 ++++ 347 ++++ 348 ++++ 349 ++++ 350 ++++ 351 ++++ 352 +++ 353 ++++ 354 + 355 + 356 ++++ 357 ++++ 358 ++++ 359 ++++ 360 ++++ 361 ++++ 362 ++++ 363 ++++ 364 ++++ 365 ++++ 366 ++++ 367 ++++ 368 ++++ 369 ++++ 370 ++++ 371 ++++ 372 ++++ 373 ++++ 374 ++++ 375 ++++ 376 ++++ 377 ++++ 378 ++++ 379 ++++ 380 ++++ 381 ++++ 382 +++ 383 ++++ 384 ++++ 385 ++++ 386 ++++ 387 ++++ 388 ++++ 389 ++++ 390 ++++ 391 ++++ 392 ++++ 393 ++++ 394 ++++ 395 ++++ 396 ++++ 397 ++++ 398 ++++ 399 ++++ 400 ++++ 401 ++++ 402 +++ 403 + 404 ++++ 405 ++++ 406 ++++ 407 ++++ 408 ++++ 409 ++++ 410 ++++ 411 ++++ 412 ++++ 413 ++++ 414 ++++ 415 ++++ 416 ++++ 417 ++++ 418 ++++ 419 ++++ 420 ++++ 421 ++++ 422 ++++ 423 ++++ 424 ++++ 425 ++++ 426 ++++ 427 ++++ 428 ++++ 429 ++++ 430 ++++ 431 +++ 432 ++++ 433 ++++ 434 ++++ 435 ++++ 436 ++++ 437 ++++ 438 ++++ 439 ++++ 440 ++++ 441 ++++ 442 ++++ 443 ++++ 444 ++++ 445 ++++ 446 ++++ 447 ++++ 448 ++++ 449 +++ 450 + 451 ++++ 452 ++++ 453 ++ 454 +++ 455 ++++ 456 ++ 457 ++++ 458 ++++ 459 +++ 460 ++++ 461 + 462 ++++ 463 ++++ 464 ++++ 465 ++++ 466 ++++ 467 ++++ 468 ++++ 469 ++++ 470 +++ 471 +++ 472 + 473 + 474 +++ 475 + 476 ++++ 477 ++++ 478 ++ 479 ++++ 480 ++++ 481 ++++ 482 ++++ 483 ++++ 484 ++++ 485 ++++ 486 ++++ 487 ++++ 488 ++++ 489 ++++ 490 ++++ 491 ++++ 492 ++++ 493 ++++ 494 ++++ 495 ++++ 496 ++++ 497 ++++ 498 ++++ 499 ++++ 500 +++ 501 ++++ 502 ++++ 503 ++++ 504 ++++ 505 ++++ 506 ++++ 507 ++++ 508 ++++ 509 ++++ 510 ++++ 511 ++++ 512 ++++ 513 ++++ 514 ++++ 515 ++++ 516 ++++ 517 ++++ 518 ++++ 519 ++++ 520 ++++ 521 ++++ 522 ++++ 523 ++++ 524 ++++ 525 ++++ 526 ++++ 527 ++++ 528 ++++ 529 ++++ 530 ++++ 531 ++++ 532 ++++ 533 ++++ 534 ++++ 535 ++++ 536 ++++ 537 ++++ 538 ++++ 539 ++++ 540 ++++ 541 ++++ 542 ++++ 543 ++++ 544 ++++ 545 ++++ 546 ++++ 547 ++++ 548 ++++ 549 + 550 ++++ 551 + 552 ++++ 553 ++++ 554 ++++ 555 ++++ 556 ++++ 557 ++++ 558 ++++ 559 ++++ 560 ++++ 561 ++++ 562 ++++ 563 ++++ 564 ++++ 565 ++++ 566 +++ 567 ++++ 568 ++++ 569 ++++ 570 ++++ 571 ++++ 572 ++++ 573 ++++ 574 ++++ 575 ++++ 576 + 577 ++++ 578 ++++ 579 ++++ 580 ++++ 581 ++++ 582 ++++ 583 ++++ 584 +++ 585 ++++ 586 ++++ 587 ++++ 588 ++++ 589 ++++ 590 ++++ 591 ++++ 592 ++++ 593 ++++ 594 ++++ 595 +++ 596 ++++ 597 ++++ 598 ++++ 599 ++++ 600 ++++ 601 ++++ 602 ++++ 603 ++++ 604 +++ 605 + 606 ++++ 607 ++++ 608 ++++ 609 ++++ 610 ++++ 611 ++++ 612 ++++ 613 ++++ 614 ++++ 615 ++++ 616 ++++ 617 ++++ 618 ++++ 619 ++++ 620 ++++ 621 ++++ 622 ++++ 623 ++++ 624 ++++ 625 ++++ 626 ++++ 627 ++++ 628 ++++ 629 ++++ 630 ++++ 631 ++++ 632 ++++ 633 ++++ 634 ++++ 635 ++++ 636 ++++ 637 ++++ 638 ++++ 639 ++++ 640 ++++ 641 ++++ 642 ++++ 643 +++ 644 ++++ 645 ++++ 646 ++++ 647 ++++ 648 ++++ 649 ++++ 650 ++++ 651 ++++ 652 ++++ 653 ++++ 654 ++++ 655 ++++ 656 ++++ 657 ++++ 658 ++++ 659 ++++ 660 ++++ 661 ++++ 662 ++++ 663 ++++ 664 ++++ 665 ++++ 666 +++

(257) IFNγ and IL-2 Analysis of Human Peripheral Pan T Cells

(258) Human peripheral blood pan T cells were purchased from STEMCELL™ Technologies Inc. Human peripheral blood pan T cells were thawed and suspended in DMEM media (10% FBS and 10 Penicillin/Streptomycin). 8×10.sup.4 T cells were seeded in 96-well plate and incubated with various concentration of compounds and 100 nM Prostaglandin E2 for 1 hr. T cells were stimulated with Dynabeads Human T-Activator CD3/CD28 (Life Technologies) at a 1:3 cells: beads ratio. Cytokine secretion was measured after 24 hr post stimulation using MSD V-PLEX human cytokine kit as suggested by the manufacturer. Data were analyzed with an MESO Quickplex SQ120 (Mesoscale Discovery).

(259) In Table 3, the values represent + for >1000 nM, ++ 200-1,000 nM, +++ for <200 nM and − for not determined.

(260) TABLE-US-00003 TABLE 3 IFNγ and IL-2 secretion of the invented compounds in human peripheral blood pan T cells Example IFNγ (EC.sub.50) IL-2 (EC.sub.50) 104 ++ + 105 ++ + 107 ++ − 110 +++ − 111 ++ − 118 +++ − 123 ++ + 125 +++ − 134 +++ + 152 ++ ++ 156 ++ ++ 161 ++ − 162 ++ − 163 − − 167 ++ + 169 ++ + 170 ++ + 172 ++ − 173 ++ − 174 ++ − 175 +++ − 178 − − 184 +++ − 193 ++ + 194 ++ − 196 ++ − 199 ++ − 258 +++ ++ 291 +++ ++ 293 +++ − 296 +++ ++ 297 +++ +++ 316 ++ + 320 ++ − 324 +++ ++ 326 ++ ++ 327 +++ ++ 329 ++ ++ 330 ++ ++ 332 ++ ++ 333 ++ ++ 334 ++ ++ 359 ++ ++ 361 ++ + 484 +++ ++ 488 ++ − 503 ++ − 509 +++ ++ 520 ++ − 521 +++ +++ 523 +++ − 524 +++ +++ 525 +++ ++ 529 +++ +++ 530 ++ ++ 531 +++ ++ 532 ++ − 534 +++ − 541 ++ − 543 +++ ++ 548 − − 550 ++ ++ 552 ++ ++ 556 +++ ++ 557 +++ ++ 558 +++ ++ 561 ++ ++ 562 ++ − 563 ++ ++ 564 ++ ++ 565 ++ ++ 569 ++ + 570 +++ ++ 574 ++ ++ 577 +++ ++ 579 +++ + 588 +++ +++