HETEROCYCLIC DERIVATIVES AND USE THEREOF

Abstract

A heterocyclic derivative represented by formula (I), or a pharmaceutically acceptable salt or a stereoisomer thereof, which has an inhibitory effect on the activation of STAT3 protein, and is useful for the prevention or treatment of diseases associated with the activation of STAT3 protein.

Claims

1. A compound selected from the group consisting of a heterocyclic derivative represented by formula (I), and a pharmaceutically acceptable salt and a stereoisomer thereof: ##STR00010## wherein one of X.sub.1, X.sub.2, X.sub.3 and X.sub.4 is —C(-Rx)=, and the others are each independently —C(-Rx′)= or —N═; one of Y and Z is —S— or —NH—, and the other is —CH═ or —N═; Rx is ##STR00011## Xs is ═O or ═NH; Ls is —C(—Rs′)(-Rs″)- or —N(-Rs′)-; Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl, C.sub.1-6alkylcarbonyl-C.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl or 5- to 10-membered heterocyclyl, or Rs is linked to Rs′ to form a chain; Rs′ and Rs″ are each independently hydrogen, halogen, C.sub.1-6alkyl, carbamoyl-C.sub.1-6alkyl, C.sub.1-6alkylamino-C.sub.1-6alkyl or diC.sub.1-6alkylamino-C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, or Rs′ is linked to Rs to form a chain; Rx′ is each independently hydrogen, halogen, nitro, amino, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, or C.sub.1-6alkylsulfonyl; A and B are each independently a monocyclic- or bicyclic-saturated or unsaturated C.sub.3-10carbocycle or 5- to 12-membered heterocycle; Rc is ═O, ═NH, ═N(—C.sub.1-6alkyl), or ═N(—OH); R.sub.N is hydrogen or C.sub.1-6alkyl, or R.sub.N is linked to R.sub.A to form a chain; L.sub.B is —[C(—R.sub.L)(—R.sub.L′)].sub.m—, —[C(—R.sub.L)(—R.sub.L′)].sub.n—O—, —O—, —NH—, —N(C.sub.1-6alkyl)-, —S(═O).sub.2—, —C(═O)—, or —C(═CH.sub.2)—, wherein m is an integer of 0 to 3, n is an integer of 1 to 3, R.sub.L and R.sub.L′ are each independently hydrogen, hydroxy, halogen or C.sub.1-6alkyl, or R.sub.L and R.sub.L′ are linked together to form a chain; R.sub.A is hydrogen, halogen, cyano, C.sub.1-6alkyl, haloC.sub.1-6alkyl, cyanoC.sub.1-6alkyl, C.sub.1-6alkylcarbonyl, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, cyanoC.sub.1-6alkoxy, C.sub.1-6alkylamino, diC.sub.1-6alkylamino, C.sub.1-6alkylthio, C.sub.1-6alkylaminocarbonyl, diC.sub.1-6alkylaminocarbonyl, C.sub.2-8alkynyl, C.sub.1-6alkoxycarbonylamino-C.sub.1-6alkoxy, aminoC.sub.1-6alkoxy or 3- to 6-membered heterocyclyl, or R.sub.A is linked to R.sub.N to form a chain; R.sub.B is hydrogen, halogen, hydroxy, cyano, nitro, amino, oxo, aminosulfonyl, sulfonylamido, C.sub.1-6alkylamino, C.sub.1-6alkyl, haloC.sub.1-6alkyl, cyanoC.sub.1-6alkyl, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, cyanoC.sub.1-6alkoxy, C.sub.3-8cycicoalkyloxy, C.sub.2-8alkenyl, C.sub.2-8alkenyloxy, C.sub.2-8alkynyl, C.sub.2-8alkynyloxy, C.sub.1-6alkylamino-C.sub.1-6alkoxy, diC.sub.1-6alkylamino-C.sub.1-6alkoxy, C.sub.1-6alkoxycarbonyl, carbamoyl, carbamoyl-C.sub.1-6alkoxy, C.sub.1-6alkylthio, C.sub.1-6alkylsulfinyl, C.sub.1-6alkylsulfonyl, 5- to 10-membered heterocyclyl, 5- to 10-membered heterocyclyl-C.sub.1-6alkyl, 5- to 10-membered heterocyclyl-C.sub.1-6alkoxy, or 5- to 10-membered heterocyclyl-oxy; p is an integer of 0 to 4, and, when p is 2 or higher, R.sub.A moieties are the same as or different from each other; q is an integer of 0 to 4, and, when q is 2 or higher, R.sub.B moieties are the same as or different from each other; and each of said chains is independently a saturated or unsaturated C.sub.2-10 hydrocarbon chain not containing or containing at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2— in the chain, and unsubstituted or substituted with at least one selected from the group consisting of halogen, C.sub.1-6alkyl and C.sub.1-6alkoxy; and each of said heterocycle and heterocyclyl moieties independently contains at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2—.

2. The compound according to claim 1, wherein one of X.sub.2 and X.sub.3 is —C(-Rx)=, and the other is —C(-Rx′)= or —N═; X.sub.1 and X.sub.4 are each independently —C(-Rx′)= or —N═; one of Y and Z is —S— or —NH—, and the other is —CH═; and Rx and Rx′ are the same as defined in claim 1.

3. The compound according to claim 2, wherein Rx is ##STR00012## Xs is ═O or ═NH; Ls is —C(—Rs′)(-Rs″)- or —N(-Rs′)-; Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl or 5- to 6-membered heterocyclyl, or Rs is linked to Rs′ to form a chain; Rs′ and Rs″ are each independently hydrogen, halogen or C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, or Rs′ is linked to Rs to form a chain; Rx′ is each independently hydrogen or halogen; and each of said chains is independently a saturated or unsaturated C.sub.2-7 hydrocarbon chain not containing or containing at least one heteroatom selected from the group consisting of O, N and S.

4. The compound according to claim 3, wherein A is benzene or a 5- to 10-membered heteroaryl containing 1 to 3 nitrogen atoms; B is a monocyclic- or bicyclic-saturated or unsaturated C.sub.6-10carbocycle or 5- to 10-membered heterocycle; L.sub.B is —[C(—R.sub.L)(—R.sub.L′)].sub.m—, —O—, —NH—, or —N(C.sub.1-6alkyl)-, wherein m is 0 or 1, R.sub.L and R.sub.L′ are each independently hydrogen, hydroxy, halogen or C.sub.1-6alkyl, or R.sub.L and R.sub.L′ are linked together to form C.sub.2-5alkylene; R.sub.A is halogen, C.sub.1-6alkoxycarbonylamino-C.sub.1-6alkoxy, aminoC.sub.1-6alkoxy, or 3- to 6-membered heterocyclyl; R.sub.B is halogen, C.sub.1-6alkyl, C.sub.1-6alkoxy, haloC.sub.1-6alkyloxy, C.sub.2-6alkenyloxy, C.sub.2-6alkynyloxy, C.sub.1-6alkoxycarbonyl, C.sub.3-10carbocyclyl-oxy, or 3- to 10-membered heterocyclyl-C.sub.1-3alkoxy; and each of said heteroaryl, heterocycle and heterocyclyl moieties independently contains 1 to 3 heteroatoms selected from the group consisting of O, N and S.

5. The compound according to claim 1, wherein X.sub.1 and X.sub.4 are —CH═; X.sub.2 is —C(-Rx)=; X.sub.3 is —N═ or —C(-Rx′)-; Y is —C═; Z is —S—; Rx is ##STR00013## Ls is —C(—CH.sub.3)(—CH.sub.3)—; Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxyC.sub.1-6alkyl, C.sub.1-6alkylcarbonylC.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl, or a 5- to 10-membered heterocyclyl containing 1 to 3 heteroatoms selected from the group consisting of O, N and S; Rx′ is hydrogen, halogen, nitro, amino, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, or C.sub.1-6alkylsulfonyl; Rc is ═O; and R.sub.N is hydrogen.

6. The compound according to claim 1, wherein X.sub.1, X.sub.3 and X.sub.4 are —CH═; X.sub.2 is —C(-Rx)=; Y is —C═; Z is —S—; Rx is ##STR00014## Ls is —C(—Rs′)(-Rs″)-; Xs is ═O or ═NH; Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl, C.sub.1-6alkylcarbonyl-C.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl, or a 5- to 10-membered heterocyclyl containing 1 to 3 heteroatoms selected from the group consisting of O, N and S; Rs′ and Rs″ are each independently hydrogen, halogen, C.sub.1-6alkyl, carbamoylC.sub.1-6alkyl, C.sub.1-6alkylamino-C.sub.1-6alkyl or diC.sub.1-6alkylamino-C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, wherein the chain is a saturated or unsaturated C.sub.2-10 hydrocarbon chain not containing or containing at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2— in the chain, and unsubstituted or substituted with at least one selected from the group consisting of halogen, C.sub.1-6alkyl and C.sub.1-6alkoxy; Rc is ═O; and R.sub.N is hydrogen.

7. The compound according to claim 1, wherein X.sub.1, X.sub.3 and X.sub.4 are —CH═; X.sub.2 is —C(-Rx)=; Y is —C═; Z is —S—; Rx is the same as defined in claim 1; Rc is ═O; and R.sub.N is hydrogen.

8. The compound according to claim 1, wherein X.sub.1, X.sub.2 and X.sub.4 are —CH═; X.sub.3 is —C(-Rx)=; Y is —C═; Z is —S— or —NH—; Rx is ##STR00015## Xs is ═O; Ls is —C(—CH.sub.3)(—CH.sub.3)—; Rs is methyl; Rc is ═O; and R.sub.N is hydrogen.

9. The compound according to claim 1, which is selected from the group consisting of: 1) N-(3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 2) N-(3-chloro-5-(2-(3-propoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 3) N-(3-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 4) N-(3-bromo-5-(2-(3-(1,1,2,2-tetrafluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 5) N-(3-chloro-5-(2-(3-(1,1,2,2-tetrafluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 6) N-(3-methoxy-5-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 7) N-(3-chloro-5-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 8) N-(3-chloro-5-(2-(3-(2-morpholinoethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 9) N-(3-bromo-5-(2-(3-isopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 10) N-(3-(2-(3-(but-2-yn-1-yloxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-chlorophenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 11) N-(3-chloro-5-(2-(3-isobutoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 12) N-(3-chloro-5-(2-(3-(2,2,2-trifluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 13) N-(3-chloro-5-(2-(3-(2,2-difluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 14) N-(3-(2-(3-(allyloxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-chlorophenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 15) N-(3-chloro-5-(2-(3-cyclopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 16) N-(3-chloro-5-(2-(3-isopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 17) N-(3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 18) N-(3-chloro-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 19) N-(3-chloro-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 20) N-(3-bromo-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 21) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 22) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 23) 6-chloro-N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 24) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 25) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 26) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxamide; 27) N-(3-chloro-5-(2-(5-chlorothiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 28) N-(3-chloro-5-(2-(5-isopropylthiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 29) N-(3-chloro-5-(2-(5-methoxythiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 30) N-(3-chloro-5-(2-(2-methoxythiophen-3-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 31) N-(3-chloro-5-(2-(1-methyl-1H-pyrrol-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 32) N-(3-chloro-5-(2-(4-methylthiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 33) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxamide; 34) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxamide; 35) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxamide; 36) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxamide; 37) N-(3-chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 38) N-(3-chloro-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 39) N-(3-bromo-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 40) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxamide; 41) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 42) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 43) N-(3-chloro-5-(4-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 44) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 45) 6-chloro-N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 46) N-(3-(4-chlorophenoxy)-5-methoxyphenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 47) N-(3-chloro-5-(3-chloro-5-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 48) N-(3-chloro-5-(3-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 49) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 50) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxamide; 51) N-(3-chloro-5-(3-chloro-4-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 52) N-(3-chloro-5-(3,4-difluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 53) N-(3-chloro-5-(3-fluoro-5-methoxyphenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 54) N-(3-chloro-5-(4-chloro-3-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 55) N-(3-chloro-5-(2-(3-chloro-5-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 56) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxamide; 57) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 58) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 59) N-(3-(azetidin-1-yl)-5-(4-chlorophenoxy)phenyl)-5-(2-(methyl sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 60) N-(3-chloro-5-((6-chloropyridin-3-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 61) N-(3-chloro-5-((5-chloropyridin-2-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 62) N-(2-chloro-6-(3,5-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 63) N-(6-chloro-4-(4-chlorophenoxy)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 64) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 65) N-(2-chloro-6-((6-chloropyridin-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 66) N-(4-chloro-6-(4-chlorophenoxy)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 67) N-(2-chloro-6-(4-(trifluoromethyl)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 68) N-(2-chloro-6-(4-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 69) N-(2-bromo-6-(4-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 70) N-(2-chloro-6-(3-chloro-5-methoxyphenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 71) N-(2-chloro-6-(3-chloro-4-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 72) N-(2-chloro-6-(4-chloro-3-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 73) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxamide; 74) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxamide; 75) N-(2-chloro-6-(4-chlorophenoxy)pyrimidin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 76) N-(6-chloro-2-(4-chlorophenoxy)pyrimidin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 77) N-(2-(4-chlorophenoxy)-6-fluoropyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 78) N-(2-(bicyclo[2.2.1]hept-5-en-2-yloxy)-6-chloropyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 79) N-(2-chloro-6-(3,4-difluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 80) N-(2-chloro-6-(3-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 81) N-(2-chloro-6-(3-(trifluoromethoxy)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 82) N-(2-chloro-6-(3,4-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 83) N-(2-chloro-6-(4-chloro-2-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 84) N-(2-chloro-6-(4-(trifluoromethoxy)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 85) N-(2-chloro-6-((5-chloropyridin-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 86) N-(2-chloro-6-((4-chlorobenzyl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 87) N-(3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 88) N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 89) N-(3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 90) N-(2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 91) N-(4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 92) N-(3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 93) tert-butyl (2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate; 94) N-(3-(2-aminoethoxy)-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 95) N-(5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; 96) (8-chloro-6-(4-chlorophenoxy)-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophen-2-yl)methanone; 97) N-(3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 98) N-(3-chloro-54(2,4-difluorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 99) N-(3-chloro-54(4-chlorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 100) N-(2-chloro-6-((4-chlorophenyl)(methyl)amino)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 101) N-(2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 102) N-(2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 103) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboximidamide 2,2,2-trifluoroacetate; 104) N-(2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 105) N-(2-(4-(tert-butyl)piperidin-1-yl)-6-chloropyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 106) N-(2-chloro-6-(octahydro-2H-pyrido[1,2-a]pyrazin-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 107) N-(2-chloro-6-(7-ethyl-2,7-diazaspiro[4.4]nonan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 108) N-(2-chloro-6-(octahydroisoquinolin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 109) N-(2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 110) N-(2-chloro-6-((1-methyl-1H-pyrazol-5-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 111) N-(2-chloro-6-((1,3,5-trimethyl-1H-pyrazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 112) N-(2-chloro-6-((1-methyl-1H-pyrazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 113) N-(2-chloro-6-((3,5-dimethylisoxazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 114) N-(2-chloro-6-((5-methylthiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 115) N-(2-chloro-6-((2-methylthiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 116) N-(2-chloro-64(4,5-dimethylisoxazol-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 117) N-(2-chloro-6-((5-(trifluoromethyl)thiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 118) methyl 3-((6-chloro-4-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)pyridin-2-yl)oxy)isoxazole-5-carboxylate; 119) N-(2-chloro-6-((4-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; 120) N-(2-chloro-6-((5-methylthiophen-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; and 121) N-(2-chloro-6-((2-chlorothiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide.

10. A pharmaceutical composition for preventing or treating diseases associated with the activation of STAT3 protein, comprising the compound as defined in claim 1 as an active ingredient.

11. The pharmaceutical composition according to claim 10, wherein the diseases associated with the activation of STAT3 protein is selected from the group consisting of solid cancers, hematological or blood cancers, radio- or chemo-resistant cancers, metastatic cancers, inflammatory diseases, immunological diseases, diabetes, macular degeneration, human papillomavirus infection and tuberculosis.

12. The pharmaceutical composition according to claim 11, wherein the diseases associated with the activation of STAT3 protein are selected from the group consisting of breast cancer, lung cancer, stomach cancer, prostate cancer, uterine cancer, ovarian cancer, kidney cancer, pancreatic cancer, liver cancer, colon cancer, skin cancer, head and neck cancer, thyroid cancer, osteosarcoma, acute or chronic leukemia, multiple myeloma, B- or T-cell lymphoma, non-Hodgkin's lymphoma, auto-immune diseases comprising rheumatoid arthritis, psoriasis, hepatitis, inflammatory bowel disease, Crohn's disease, diabetes, macular degeneration, human papillomavirus infection, and tuberculosis.

13. A use of the compound as defined in claim 1 for the manufacture of a medicament for preventing or treating diseases associated with the activation of STAT3 protein.

14. A method for preventing or treating diseases associated with the activation of STAT3 protein in a mammal, which comprises administering the compound as defined in claim 1 to the mammal.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0032] The present invention will be further described in detail herein below.

[0033] In the specification of the present invention, the term “halogen” refers to fluoro, chloro, bromo or iodo, unless specified otherwise.

[0034] The term “alkyl” refers to a linear or branched hydrocarbon moiety, unless specified otherwise.

[0035] The terms “haloalkyl”, “haloalkoxy”, “halophenyl”, etc., respectively refer to alkyl, alkoxy, and phenyl substituted with at least one halogen.

[0036] The term “carbocycle” refers to an aromatic or non-aromatic hydrocarbon ring, which may be saturated or unsaturated, and a monocyclic or polycyclic radical. The term “carbocyclyl” refers to a radical of “carbocycle”, and is used as a term inclusive of “cycloalkyl” and “aryl”. The term “cycloalkyl” refers to a saturated hydrocarbon radical, which may be monocyclic or polycyclic. The term “aryl” refers to an aromatic hydrocarbon ring, which may be monocyclic or polycyclic.

[0037] The terms “carbocycle”, “carbocyclyl”, “cycloalkyl” and “aryl” may refer to, for example, a monocycle or polycycle having 3 to 20 carbon atoms, and will be indicated as “C.sub.3-20 carbocycle”, “C.sub.3-20 carbocyclyl”, “C.sub.3-20 cycloalkyl”, and “C.sub.3-20 aryl”, respectively.

[0038] The term “heterocycle” refers to an aromatic or non-aromatic ring having at least one heteroatom, which may be saturated or unsaturated, and a monocycle or polycycle. The term “heterocyclyl” refers to a radical of “heterocycle”, which is used as a term inclusive of “heterocycloalkyl” and “heteroaryl”. The term “heterocycloalkyl” refers to a saturated ring radical having at least one heteroatom, which may be monocyclic or polycyclic. The term “heteroaryl” refers to an aromatic ring radical having at least one heteroatom, which may be monocyclic or polycyclic.

[0039] The term “heteroatom” may be selected from N, O and S.

[0040] The terms “heterocycle”, “heterocyclyl”, “heterocycloalkyl” and “heteroaryl” may refer to, for example, a mono- or polycycle having 3 to 20 heteroatoms and/or carbon atoms, and will be indicated as “3- to 20-membered heterocycle”, “3- to 20-membered heterocyclyl”, “3- to 20-membered heterocycloalkyl”, and “3- to 20-membered heteroaryl”.

[0041] The term “chain” refers to a saturated or unsaturated C.sub.2-10 hydrocarbon chain not containing any heteroatoms in the chain, for example, ethylene, propylene, butylene and —CH.sub.2—CH═CH—; or a saturated or unsaturated C.sub.2-10 hydrocarbon chain containing at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2— in the chain, for example, —CH.sub.2—O—CH.sub.2—, —CH.sub.2—O—CH.sub.2—O—CH.sub.2—, —CH.sub.2—CH═CH—NH— and —CH.sub.2—CH.sub.2—S(═O).sub.2—CH.sub.2—O—, unless specified otherwise. The chain may be substituted with at least one selected from the group consisting of halogen, C.sub.1-6alkyl and C.sub.1-6alkoxy.

[0042] In accordance with one aspect of the present invention, there is provided a compound selected from the group consisting of a heterocyclic derivative represented by formula (I), and a pharmaceutically acceptable salt and a stereoisomer thereof:

##STR00003##

[0043] wherein

[0044] one of X.sub.1, X.sub.2, X.sub.3 and X.sub.4 is —C(-Rx)=, and the others are each independently —C(-Rx′)=or —N═;

[0045] one of Y and Z is —S— or —NH—, and the other is —CH═ or —N═;

[0046] Rx is

##STR00004##

[0047] Xs is ═O or ═NH;

[0048] Ls is —C(—Rs′)(-Rs″)- or —N(-Rs′)-;

[0049] Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl, C.sub.1-6alkylcarbonyl-C.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl or 5- to 10-membered heterocyclyl, or Rs is linked to Rs′ to form a chain;

[0050] Rs′ and Rs″ are each independently hydrogen, halogen, C.sub.1-6alkyl, carbamoyl-C.sub.1-6alkyl, C.sub.1-6alkylamino-C.sub.1-6alkyl or diC.sub.1-6alkylamino-C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, or Rs′ is linked to Rs to form a chain;

[0051] Rx′ is each independently hydrogen, halogen, nitro, amino, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, or C.sub.1-6alkylsulfonyl;

[0052] A and B are each independently a monocyclic- or bicyclic-saturated or unsaturated C.sub.3-10carbocycle or 5- to 12-membered heterocycle;

[0053] Rc is ═O, ═NH, —N(—C.sub.1-6alkyl), or ═N(—OH);

[0054] R.sub.N is hydrogen or C.sub.1-6alkyl, or R.sub.N is linked to R.sub.A to form a chain;

[0055] L.sub.B is —[C(—R.sub.L)(—R.sub.L′)].sub.m—, —[C(—R.sub.L)(—R.sub.L′)].sub.n—O—, —O—, —NH—, —N(C.sub.1-6alkyl)-, —S(═O).sub.2—, —C(═O)—, or —C(═CH.sub.2)—, wherein m is an integer of 0 to 3, n is an integer of 1 to 3, R.sub.L and R.sub.L′ are each independently hydrogen, hydroxy, halogen or C.sub.1-6alkyl, or R.sub.L and R.sub.L′ are linked together to form a chain;

[0056] R.sub.A is hydrogen, halogen, cyano, C.sub.1-6alkyl, haloC.sub.1-6alkyl, cyanoC.sub.1-6alkyl, C.sub.1-6alkylcarbonyl, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, cyanoC.sub.1-6alkoxy, C.sub.1-6alkylamino, diC.sub.1-6alkylamino, C.sub.1-6alkylthio, C.sub.1-6alkylaminocarbonyl, diC.sub.1-6alkylaminocarbonyl, C.sub.2-8alkynyl, C.sub.1-6 alkoxycarbonylamino-C.sub.1-6alkoxy, aminoC.sub.1-6alkoxy or 3- to 6-membered heterocyclyl, or R.sub.A is linked to R.sub.N to form a chain;

[0057] R.sub.B is hydrogen, halogen, hydroxy, cyano, nitro, amino, oxo, aminosulfonyl, sulfonylamido, C.sub.1-6alkylamino, C.sub.1-6alkyl, haloC.sub.1-6alkyl, cyanoC.sub.1-6alkyl, C.sub.1-6alkoxy, halo C.sub.1-6alkoxy, cyanoC.sub.1-6alkoxy, C.sub.3-8cyclcoalkyloxy, C.sub.2-8alkenyl, C.sub.2-8alkenyloxy, C.sub.2-8alkynyl, C.sub.2-8alkynyloxy, C.sub.1-6alkylamino-C.sub.1-6alkoxy, diC.sub.1-6alkylamino-C.sub.1-6alkoxy, C.sub.1-6alkoxycarbonyl, carbamoyl, carbamoyl-C.sub.1-6alkoxy, C.sub.1-6alkylthio, C.sub.1-6alkylsulfinyl, C.sub.1-6alkylsulfonyl, 5- to 10-membered heterocyclyl, 5- to 10-membered heterocyclyl-C.sub.1-6alkyl, 5- to 10-membered heterocyclyl-C.sub.1-6alkoxy, or 5- to 10-membered heterocyclyl-oxy;

[0058] p is an integer of 0 to 4, and, when p is 2 or higher, R.sub.A moieties are the same as or different from each other;

[0059] q is an integer of 0 to 4, and, when q is 2 or higher, R.sub.B moieties are the same as or different from each other; and

[0060] each of said chains is independently a saturated or unsaturated C.sub.2-10 hydrocarbon chain not containing or containing at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2— in the chain, and unsubstituted or substituted with at least one selected from the group consisting of halogen, C.sub.1-6alkyl and C.sub.1-6alkoxy; and

[0061] each of said heterocycle and heterocyclyl moieties independently contains at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2—.

[0062] In a preferred embodiment of the compound of formula (I),

[0063] one of X.sub.2 and X.sub.3 is —C(-Rx)=, and the other is —C(-Rx′)= or —N═;

[0064] X.sub.1 and X.sub.4 are each independently —C(-Rx′)= or —N═;

[0065] one of Y and Z is —S— or —NH—, and the other is —CH═;

[0066] Rx and Rx′ are the same as defined above in formula (I); and

[0067] Rc, R.sub.N, A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0068] In a preferred embodiment of the compound of formula (I),

[0069] one of X.sub.2 and X.sub.3 is —C(-Rx)=, and the other is —C(-Rx′)= or —N═;

[0070] X.sub.1 and X.sub.4 are each independently —C(-Rx′)= or —N═;

[0071] one of Y and Z is —S— or —NH—, and the other is —CH═;

[0072] Rx is

##STR00005##

[0073] Xs is ═O or ═NH;

[0074] Ls is —C(—Rs′)(-Rs″)- or —N(-Rs′)-;

[0075] Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6 alkyl or 5- to 6-membered heterocyclyl, or Rs is linked to Rs′ to form a chain;

[0076] Rs′ and Rs″ are each independently hydrogen, halogen or C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, or Rs′ is linked to Rs to form a chain;

[0077] Rx′ is each independently hydrogen or halogen;

[0078] each of said chains is independently a saturated or unsaturated C.sub.2-7 hydrocarbon chain not containing or containing at least one heteroatom selected from the group consisting of O, N and S; and

[0079] Rc, R.sub.N, A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0080] In a preferred embodiment of the compound of formula (I),

[0081] one of X.sub.2 and X.sub.3 is —C(-Rx)=, and the other is —C(-Rx′)= or

[0082] X.sub.1 and X.sub.4 are each independently —C(-Rx′)= or —N═;

[0083] one of Y and Z is —S— or —NH—, and the other is —CH═;

[0084] Rx is

##STR00006##

[0085] Xs is ═O or ═NH;

[0086] Ls is —C(—Rs′)(-Rs″)- or —N(-Rs′)-;

[0087] Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl or 5- to 6-membered heterocyclyl, or Rs is linked to Rs′ to form a chain;

[0088] Rs′ and Rs″ are each independently hydrogen, halogen or C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, or Rs′ is linked to Rs to form a chain;

[0089] Rx′ is each independently hydrogen or halogen;

[0090] each of said chains is independently a saturated or unsaturated C.sub.2-7 hydrocarbon chain not containing or containing at least one heteroatom selected from the group consisting of O, N and S;

[0091] Rc and R.sub.N are the same as defined above in formula (I);

[0092] A is benzene or a 5- to 10-membered heteroaryl containing 1 to 3 nitrogen atoms;

[0093] B is a monocyclic- or bicyclic-saturated or unsaturated C.sub.6-10carbocycle or 5- to 10-membered heterocycle;

[0094] L.sub.B is —[C(—R.sub.L)(—R.sub.L)].sub.m—, —O—, —NH—, or —N(C.sub.1-6alkyl)-, wherein m is 0 or 1, R.sub.L and R.sub.L′ are each independently hydrogen, hydroxy, halogen or C.sub.1-6alkyl, or R.sub.L and R.sub.L′ are linked together to form C.sub.2-5alkylene;

[0095] R.sub.A is halogen, C.sub.1-6alkoxycarbonylamino-C.sub.1-6alkoxy, aminoC.sub.1-6alkoxy, or 3- to 6-membered heterocyclyl;

[0096] R.sub.B is halogen, C.sub.1-6alkyl, C.sub.1-6alkoxy, haloC.sub.1-6alkyloxy, C.sub.2-6alkenyloxy, C.sub.2-6alkynyloxy, C.sub.1-6alkoxycarbonyl, C.sub.3-10carbocyclyl-oxy, or 3- to 10-membered heterocyclyl-C.sub.1-3alkoxy; and

[0097] each of said heteroaryl, heterocycle and heterocyclyl moieties independently contains 1 to 3 heteroatoms selected from the group consisting of O, N and S.

[0098] In a preferred embodiment of the compound of formula (I),

[0099] X.sub.1 and X.sub.4 are —CH═;

[0100] X.sub.2 is —C(-Rx)=;

[0101] X.sub.3 is —N═ or —C(-Rx′)-;

[0102] Y is —C;

[0103] Z is —S—;

[0104] Rx is

##STR00007##

[0105] Ls is —C(—CH.sub.3)(—CH.sub.3)—;

[0106] Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxyC.sub.1-6 alkyl, C.sub.1-6alkylcarbonylC.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl, or a 5- to 10-membered heterocyclyl containing 1 to 3 heteroatoms selected from the group consisting of O, N and S;

[0107] Rx′ is hydrogen, halogen, nitro, amino, C.sub.1-6alkoxy, haloC.sub.1-6alkoxy, or C.sub.1-6alkylsulfonyl;

[0108] Rc is ═O;

[0109] R.sub.N is hydrogen; and

[0110] A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0111] In a preferred embodiment of the compound of formula (I),

[0112] X.sub.1, X.sub.3 and X.sub.4 are —CH═;

[0113] X.sub.2 is —C(-Rx)=;

[0114] Y is —C═;

[0115] Z is —S—;

[0116] Rx is

##STR00008##

[0117] Ls is —C(—Rs′)(-Rs″)-;

[0118] Xs is ═O or ═NH;

[0119] Rs is C.sub.1-6alkyl, haloC.sub.1-6alkyl, C.sub.1-6alkoxy-C.sub.1-6alkyl, C.sub.1-6alkylcarbonyl-C.sub.1-6alkyl, C.sub.2-7alkenyl, amino, aminoC.sub.1-6alkyl, or a 5- to 10-membered heterocyclyl containing 1 to 3 heteroatoms selected from the group consisting of O, N and S;

[0120] Rs′ and Rs″ are each independently hydrogen, halogen, C.sub.1-6alkyl, carbamoylC.sub.1-6alkyl, C.sub.1-6alkylamino-C.sub.1-6alkyl or diC.sub.1-6alkylamino-C.sub.1-6alkyl, or Rs′ and Rs″ are linked together to form a chain, wherein the chain is a saturated or unsaturated C.sub.2-10 hydrocarbon chain not containing or containing at least one heterogroup selected from the group consisting of —O—, —NH—, —N═, —S—, —S(═O)— and —S(═O).sub.2— in the chain, and unsubstituted or substituted with at least one selected from the group consisting of halogen, C.sub.1-6alkyl and C.sub.1-6alkoxy;

[0121] Rc is ═O;

[0122] R.sub.N is hydrogen; and

[0123] A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0124] In a preferred embodiment of the compound of formula (I),

[0125] X.sub.1, X.sub.3 and X.sub.4 are —CH═;

[0126] X.sub.2 is —C(-Rx)=;

[0127] Y is —C═;

[0128] Z is —S—;

[0129] Rx is the same as defined above in formula (I);

[0130] Rc is ═O;

[0131] R.sub.N is hydrogen; and

[0132] A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0133] In a preferred embodiment of the compound of formula (I),

[0134] X.sub.1, X.sub.2 and X.sub.4 are —CH═;

[0135] X.sub.3 is —C(-Rx)=;

[0136] Y is —C═;

[0137] Z is —S— or —NH—;

[0138] Rx is

##STR00009##

[0139] Xs is ═O;

[0140] Ls is —C(—CH.sub.3)(—CH.sub.3)—;

[0141] Rs is methyl;

[0142] Rc is ═O;

[0143] R.sub.N is hydrogen; and

[0144] A, B, L.sub.B, R.sub.A, R.sub.B, p and q are the same as defined above in formula (I).

[0145] In a preferred embodiment of the compound of formula (I), if A is 5-membered heterocycle, m is an integer of 1 to 3. The 5-membered heterocycle is preferably a 5-membered aromatic ring unsubstituted or substituted with at least one selected from the group consisting of halogen, C.sub.1-10alkyl and haloC.sub.1-10alkyl. The 5-membered heterocycle contains at least one heteroatom selected from the group consisting of N, S and O.

[0146] Preferable examples of the compound according to the present invention are listed below, and a pharmaceutically acceptable salt and a stereoisomer thereof are also included in the scope of the present invention: [0147] 1) N-(3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0148] 2) N-(3-chloro-5-(2-(3-propoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0149] 3) N-(3-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0150] 4) N-(3-bromo-5-(2-(3-(1,1,2,2-tetrafluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0151] 5) N-(3-chloro-5-(2-(3-(1,1,2,2-tetrafluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0152] 6) N-(3-methoxy-5-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0153] 7) N-(3-chloro-5-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0154] 8) N-(3-chloro-5-(2-(3-(2-morpholinoethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0155] 9) N-(3-bromo-5-(2-(3-isopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0156] 10) N-(3-(2-(3-(but-2-yn-1-yloxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-chlorophenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0157] 11) N-(3-chloro-5-(2-(3-isobutoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0158] 12) N-(3-chloro-5-(2-(3-(2,2,2-trifluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0159] 13) N-(3-chloro-5-(2-(3-(2,2-difluoroethoxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0160] 14) N-(3-(2-(3-(allyloxy)-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-chlorophenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0161] 15) N-(3-chloro-5-(2-(3-cyclopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0162] 16) N-(3-chloro-5-(2-(3-isopropoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0163] 17) N-(3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0164] 18) N-(3-chloro-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0165] 19) N-(3-chloro-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0166] 20) N-(3-bromo-5-(2-(4-fluorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0167] 21) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0168] 22) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0169] 23) 6-chloro-N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0170] 24) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0171] 25) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0172] 26) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxamide; [0173] 27) N-(3-chloro-5-(2-(5-chlorothiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0174] 28) N-(3-chloro-5-(2-(5-isopropylthiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0175] 29) N-(3-chloro-5-(2-(5-methoxythiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0176] 30) N-(3-chloro-5-(2-(2-methoxythiophen-3-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0177] 31) N-(3-chloro-5-(2-(1-methyl-1H-pyrrol-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0178] 32) N-(3-chloro-5-(2-(4-methylthiophen-2-yl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0179] 33) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxamide; [0180] 34) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxamide; [0181] 35) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxamide; [0182] 36) N-(3-chloro-5-(2-(4-chlorophenyl)propan-2-yl)phenyl)-5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxamide; [0183] 37) N-(3-chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0184] 38) N-(3-chloro-5-(4-(trifluoromethyl)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0185] 39) N-(3-bromo-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0186] 40) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxamide; [0187] 41) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0188] 42) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0189] 43) N-(3-chloro-5-(4-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0190] 44) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0191] 45) 6-chloro-N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0192] 46) N-(3-(4-chlorophenoxy)-5-methoxyphenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0193] 47) N-(3-chloro-5-(3-chloro-5-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0194] 48) N-(3-chloro-5-(3-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0195] 49) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0196] 50) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxamide; [0197] 51) N-(3-chloro-5-(3-chloro-4-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0198] 52) N-(3-chloro-5-(3,4-difluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0199] 53) N-(3-chloro-5-(3-fluoro-5-methoxyphenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0200] 54) N-(3-chloro-5-(4-chloro-3-fluorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0201] 55) N-(3-chloro-5-(2-(3-chloro-5-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0202] 56) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxamide; [0203] 57) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0204] 58) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0205] 59) N-(3-(azetidin-1-yl)-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0206] 60) N-(3-chloro-5-((6-chloropyridin-3-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0207] 61) N-(3-chloro-5-((5-chloropyridin-2-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0208] 62) N-(2-chloro-6-(3,5-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0209] 63) N-(6-chloro-4-(4-chlorophenoxy)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0210] 64) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0211] 65) N-(2-chloro-6-((6-chloropyridin-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0212] 66) N-(4-chloro-6-(4-chlorophenoxy)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0213] 67) N-(2-chloro-6-(4-(trifluoromethyl)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0214] 68) N-(2-chloro-6-(4-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0215] 69) N-(2-bromo-6-(4-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0216] 70) N-(2-chloro-6-(3-chloro-5-methoxyphenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0217] 71) N-(2-chloro-6-(3-chloro-4-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0218] 72) N-(2-chloro-6-(4-chloro-3-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0219] 73) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxamide; [0220] 74) N-(2-chloro-6-(4-chlorophenoxy)pyridin-4-yl)-5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxamide; [0221] 75) N-(2-chloro-6-(4-chlorophenoxy)pyrimidin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0222] 76) N-(6-chloro-2-(4-chlorophenoxy)pyrimidin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0223] 77) N-(2-(4-chlorophenoxy)-6-fluoropyrdin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0224] 78) N-(2-(bicyclo[2.2.1]hept-5-en-2-yloxy)-6-chloropyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0225] 79) N-(2-chloro-6-(3,4-difluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0226] 80) N-(2-chloro-6-(3-chlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0227] 81) N-(2-chloro-6-(3-(trifluoromethoxy)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0228] 82) N-(2-chloro-6-(3,4-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0229] 83) N-(2-chloro-6-(4-chloro-2-fluorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0230] 84) N-(2-chloro-6-(4-(trifluoromethoxy)phenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0231] 85) N-(2-chloro-6-((5-chloropyridin-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0232] 86) N-(2-chloro-6-((4-chlorobenzyl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0233] 87) N-(3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0234] 88) N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0235] 89) N-(3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0236] 90) N-(2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0237] 91) N-(4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0238] 92) N-(3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0239] 93) tert-butyl (2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate; [0240] 94) N-(3-(2-aminoethoxy)-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0241] 95) N-(5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-5-((methyl sulfonyl)methyl)benzo[b]thiophene-2-carboxamide; [0242] 96) (8-chloro-6-(4-chlorophenoxy)-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophen-2-yl)methanone; [0243] 97) N-(3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0244] 98) N-(3-chloro-5-((2,4-difluorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0245] 99) N-(3-chloro-5-((4-chlorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0246] 100) N-(2-chloro-6-((4-chlorophenyl)(methyl)amino)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0247] 101) N-(2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0248] 102) N-(2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0249] 103) N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboximidamide 2,2,2-trifluoroacetate; [0250] 104) N-(2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0251] 105) N-(2-(4-(tert-butyl)piperidin-1-yl)-6-chloropyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0252] 106) N-(2-chloro-6-(octahydro-2H-pyrido[1,2-a]pyrazin-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0253] 107) N-(2-chloro-6-(7-ethyl-2,7-diazaspiro[4.4]nonan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0254] 108) N-(2-chloro-6-(octahydroisoquinolin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0255] 109) N-(2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0256] 110) N-(2-chloro-6-((1-methyl-1H-pyrazol-5-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0257] 111) N-(2-chloro-6-((1,3,5-trimethyl-1H-pyrazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0258] 112) N-(2-chloro-6-((1-methyl-1H-pyrazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0259] 113) N-(2-chloro-6-((3,5-dimethylisoxazol-4-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0260] 114) N-(2-chloro-6-((5-methylthiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0261] 115) N-(2-chloro-6-((2-methylthiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0262] 116) N-(2-chloro-6-((4,5-dimethylisoxazol-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0263] 117) N-(2-chloro-6-((5-(trifluoromethyl)thiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0264] 118) methyl 3-((6-chloro-4-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)pyridin-2-yl)oxy)isoxazole-5-carboxylate; [0265] 119) N-(2-chloro-6-((4-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; [0266] 120) N-(2-chloro-6-((5-methylthiophen-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide; and [0267] 121) N-(2-chloro-6-((2-chlorothiophen-3-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide.

[0268] The above-listed names of the compounds are described in accordance with the nomenclature method provided by ChemBioDraw Ultra software (Version 13.0.0.3015) of PerkinElmer.

[0269] The present invention provides a pharmaceutically acceptable salt of a heterocyclic derivative represented by formula (I) above. The pharmaceutically acceptable salt should have low toxicity to humans, and should not have any negative impact on the biological activities and physicochemical properties of parent compounds. Examples of the pharmaceutically acceptable salt may include an acid addition salt between a pharmaceutically usable free acid and a basic compound represented by formula (I), an alkaline metal salt (sodium salt, etc.) and an alkaline earth metal salt (potassium salt, etc.), an organic base addition salt between an organic base and carboxylic acid represented by formula (I), amino acid addition salt, etc.

[0270] Examples of a suitable form of salts according to the present invention may be a salt with an inorganic acid or organic acid, wherein the inorganic acid may be hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, perchloric acid, bromic acid, etc., and the organic acid may be acetic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, fumaric acid, maleic acid, malonic acid, phthalic acid, succinic acid, lactic acid, citric acid, gluconic acid, tartaric acid, salicylic acid, malic acid, oxalic acid, benzoic acid, embonic acid, aspartic acid, glutamic acid, etc. The organic base which may be used for the preparation of the organic base addition salt may include tris(hydroxymethyl)methylamine, dicyclohexylamine, etc. Amino acids which may be used for the preparation of amino acid addition base may include natural amino acids such as alanine, and glycine.

[0271] The salts may be prepared using a conventional method. For example, the salts may be prepared by dissolving the compound represented by formula (I) in a water-miscible solvent such as methanol, ethanol, acetone, and 1,4-dioxane, adding a free acid or a free base, and then crystallizing the resultant thereafter.

[0272] Additionally, the compounds of the present invention may have a chiral carbon center, and thus they may be present in the form of an R or S isomer, a racemic compound, an individual enantiomer or a mixture, an individual diastereomer or a mixture, and all these stereoisomers and a mixture thereof may belong to the scope of the present invention.

[0273] Additionally, the compounds of the present invention may also include a hydrate or solvate of the heterocyclic derivative represented by formula (I). The hydrate or solvate may be prepared using a known method, and they are preferred to be non-toxic and water-soluble, and in particular, they are preferably water or a hydrate or solvate having 1-5 molecules of alcoholic solvent (especially ethanol, etc.) bound thereto.

[0274] The present invention also provides a use of a compound selected from the group consisting of a heterocyclic derivative represented by formula (I) above, and a pharmaceutically acceptable salt and a stereoisomer thereof for the manufacture of a medicament for preventing or treating diseases associated with the activation of STAT3 protein.

[0275] Further, the present invention provides method for preventing or treating diseases associated with the activation of STAT3 protein in a mammal, which comprises administering a compound selected from the group consisting of a heterocyclic derivative represented by formula (I) above, and a pharmaceutically acceptable salt and a stereoisomer thereof to the mammal.

[0276] Further, the present invention provides a pharmaceutical composition for preventing or treating diseases associated with the activation of STAT3 protein, comprising a compound selected from the group consisting of a heterocyclic derivative represented by formula (I) above, and a pharmaceutically acceptable salt and a stereoisomer thereof as active ingredients.

[0277] Specifically, the diseases associated with the activation of STAT3 protein is selected from the group consisting of solid cancers, hematological or blood cancers, radio- or chemo-resistant cancers, metastatic cancers, inflammatory diseases, immunological diseases, diabetes, macular degeneration, human papillomavirus infection and tuberculosis.

[0278] More specifically, the diseases associated with the activation of STAT3 protein are selected from the group consisting of breast cancer, lung cancer, stomach cancer, prostate cancer, uterine cancer, ovarian cancer, kidney cancer, pancreatic cancer, liver cancer, colon cancer, skin cancer, head and neck cancer, thyroid cancer, osteosarcoma, acute or chronic leukemia, multiple myeloma, B- or T-cell lymphoma, non-Hodgkin's lymphoma, auto-immune diseases comprising rheumatoid arthritis, psoriasis, hepatitis, inflammatory bowel disease, Crohn's disease, diabetes, macular degeneration, human papillomavirus infection, and tuberculosis.

[0279] In particular, a heterocyclic derivative represented by formula (I) above, or a pharmaceutically acceptable salt or a stereoisomer thereof has an excellent inhibitory effect on the activation of STAT3 protein, and thus the present invention also provides a composition for the inhibition of STAT3 protein comprising the same as an active ingredient.

[0280] The pharmaceutical composition of the present invention, in addition to the heterocyclic derivative represented by formula (I) above, the pharmaceutically acceptable salt thereof, or the stereoisomer thereof, may further include as active ingredients, common and non-toxic pharmaceutically acceptable additives, for example, a carrier, an excipient, a diluent, an adjuvant, etc., to be formulated into a preparation according to a conventional method.

[0281] The pharmaceutical composition of the present invention may be formulated into various forms of preparations for oral administration such as tablets, pills, powders, capsules, syrups, or emulsions, or for parenteral administration such as intramuscular, intravenous or subcutaneous injections, etc., and preferably in the form of a preparation for oral administration.

[0282] Examples of the additives to be used in the pharmaceutical composition of the present invention may include sweeteners, binders, solvents, solubilization aids, wetting agents, emulsifiers, isotonic agents, absorbents, disintegrating agents, antioxidants, preservatives, lubricants, fillers, flavoring agents, etc. For example, they may include, lactose, dextrose, sucrose, mannitol, sorbitol, cellulose, glycine, silica, talc, stearic acid, stearin, magnesium stearate, magnesium alluminosilicate, starch, gelatin, gum tragacanth, alginic acid, sodium alginate, methylcellulose, sodium carboxymethylcellulose, agar, water, ethanol, polyethylene glycol, polyvinylpyrrolidone, sodium chloride, calcium chloride, orange essence, strawberry essence, vanilla flavor, etc.

[0283] The pharmaceutical composition of the present invention may be formulated into a preparation for oral administration by adding additives to active ingredients, wherein the additives may include cellulose, calcium silicate, corn starch, lactose, sucrose, dextrose, calcium phosphate, stearic acid, magnesium stearate, calcium stearate, gelatin, talc, surfactants, suspension agents, emulsifiers, diluents, etc.

[0284] The pharmaceutical composition of the present invention may be formulated into a preparation for injection by adding additives to the active ingredients, for example, water, a saline solution, a glucose solution, an aqueous glucose solution analog, alcohol, glycol, ether, oil, fatty acid, fatty acid ester, glyceride, surfactants, suspension agents, emulsifiers, etc.

[0285] The compound of the present invention may be administered preferably in an amount ranging from 0.1 to 2,000 mg/day based on an adult subject with 70 kg body weight. The compound of the present invention may be administered once daily or a few divided doses. The dosage of the compound of the present invention may vary depending on the health conditions, age, body weight, sex of the subject, administration route, severity of illness, etc., and the scope of the present invention will not be limited to the dose suggested above.

EXAMPLE

[0286] Hereinafter, the present invention is described more specifically by the following examples, but these are provided only for illustration purposes and the present invention is not limited thereto.

[0287] The definition of the abbreviations used in the following examples is as follows.

TABLE-US-00001 TABLE 1 Abbreviation Full name AlCl.sub.3 Aluminum chloride AcOH Acetic acid AIBN 2,2′-Azobis(2-methylpropionitrile) BINAP 2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl BBr.sub.3 Boron tribromide Brine Brine is water saturated or nearly saturated with a brine salt (generally, sodium chloride) n-BuLi n-butyllithium tert-BuLi tert-butyllithium tert-BuOH tert-buthyl alcohol CH.sub.3CN Acetonitrile CHCl.sub.3 Chloroform CHBr.sub.3 Bromoform CDCl.sub.3 Deuterated chloroform CH.sub.2Cl.sub.2 Dichloromethane CH.sub.3I Methyl iodide (COCl).sub.2 Oxalyl chloride Cs.sub.2CO.sub.3 Cesium carbonate CuI Copper (I) iodide Cu.sub.2O Copper (I) oxide DBU 1,8-Diazabicyclo[5.4.0]undec-7-ene DEAD Diethyl azodicarboxylate DIPEA N,N-diisopropylethylamine DME 1,2-Dimethoxyethane DMF N,N-dimethylformamide DMSO Dimethylsulfoxide DMSO-d.sub.6 Dimethylsulfoxide-d.sub.6 EtOAc Ethyl acetate EtOH Ethyl alcohol Et.sub.2O Diethyl ether HATU 2-(7-Aza-1H-benzotriazole-1-yl)-1,1,3,3- tetramethyluronium hexafluorophosphate HBr Hydrogen bromide HCl Hydrogen chloride n-Hex n-Hexane H.sub.2O Water H.sub.2O.sub.2 Hydrogen peroxide K.sub.2CO.sub.3 Potassium carbonate KOH Potassium hydroxide LiAlH.sub.4 Lithium aluminum hydride LiOHH.sub.2O Lithium hydroxide, monohydrate MeOH Methyl alcohol Na.sub.2CO.sub.3 Sodium carbonate Na.sub.2SO.sub.4 Sodium sulfate NaH Sodium hydride NaHCO.sub.3 Sodium bicarbonate NaHSO.sub.4 Sodium bisulfate NaH.sub.2PO.sub.4 Sodium phosphate monobasic acid NaIO.sub.4 Sodium periodate NaN.sub.3 Sodium azide NaOH Sodium hydroxide NaOMe Sodium methoxide NaOt-Bu Sodium tert-butoxide NH.sub.4Cl Ammonium chloride Pd(dba).sub.2 Bis(dibenzylideneacetone)palladium(0) Pd(PPh.sub.3).sub.4 Tetrakis(triphenylphosphine)palladium(0) Pd(OAc).sub.2 Palladium(II) acetate PCl.sub.3 Phosphorus trichloride PCl.sub.5 Phosphorus pentachloride PPh.sub.3 Triphenylphosphine RuCl.sub.3H.sub.2O Ruthenium(III) chloride hydrate SOCl.sub.2 Thionyl chloride Tf.sub.2O Trifluoromethanesulfonic anhydride THF Tetrahydrofuran TiCl.sub.4 Titanium tetrachloride TFA Trifluoroacetic acid XPhos 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene Zn Zinc ZnBr.sub.2 Zinc bromide ZnCl.sub.2 Zinc chloride

Intermediate 1) Synthesis of 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 1-(bromomethyl)-2,4-difluoro-5-methylbenzene

[0288] Paraformaldehyde (247.0 mg, 7.81 mmol) was dissolved in 33% solution of HBr in AcOH (4.0 mL), and 2,4-difluoro-1-methylbenzene (1.0 g, 7.81 mmol) and ZnBr.sub.2 (880.0 mg, 3.91 mmol) were added. The reaction mixture was stirred at 120° C. for 4 hours, cooled to room temperature, sat. NaHCO.sub.3 was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 1-(bromomethyl)-2,4-difluoro-5-methylbenzene (1.1 g, 64%) as a colorless liquid.

[0289] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.20 (t, 1H, J=8.4 Hz), 6.77 (t, 1H, J=9.5 Hz), 4.46 (s, 2H), 2.24 (s, 3H)

(b) Synthesis of 1,5-difluoro-2-methyl-4-((methylsulfonyl)methyl)benzene

[0290] 1-(Bromomethyl)-2,4-difluoro-5-methylbenzene (260.0 mg, 1.18 mmol) was dissolved in anhydrous EtOH (6.0 mL) and sodium methanesulfinate (120.0 mg, 1.18 mmol) was added. The reaction mixture was refluxed for 2 hours, cooled to room temperature, and concentrated under reduced pressure. The residue was recrystallized with Et.sub.2O to obtain 1,5-difluoro-2-methyl-4-((methylsulfonyl)methyl)benzene (160.0 mg, 61%) as a white solid.

[0291] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.32 (t, 1H, J=8.3 Hz), 6.86 (t, 1H, J=9.5 Hz), 4.24 (s, 2H), 2.82 (s, 3H), 2.27 (s, 3H)

[0292] 1,5-Difluoro-2-methyl-4-((methylsulfonyl)methyl)benzene (3.4 g, 15.40 mmol) was dissolved in anhydrous DMF (22.4 mL), and NaOt-Bu (3.7 g, 38.60 mmol) and CH.sub.3I (4.8 mL, 77.20 mmol) were added at 0° C. The reaction mixture was stirred at 0° C., H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=4:1) to obtain 1,5-difluoro-2-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (370.0 mg, 10%) as a white solid.

[0293] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.38 (t, 1H, J=9.2 Hz), 6.75 (t, 1H, J=9.2 Hz), 2.70-2.81 (m, 3H), 1.90 (s, 3H), 1.74 (d, 6H, J=7.2 Hz)

(d) Synthesis of 1-(bromomethyl)-2,4-difluoro-5-(2-(methylsulfonyl)propan-2-yl)benzene

[0294] 1,5-Difluoro-2-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (370.0 mg, 1.49 mmol) was dissolved in anhydrous 1,2-dichloroethane (15.0 mL), and N-bromosuccinimide (265.0 mg, 1.49 mmol) and AIBN (25.0 mg, 0.15 mmol) were added. The reaction mixture was refluxed at 100° C. for 15 hours, cooled to room temperature, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by silica column chromatography (n-Hex:EtOAc=4:1) to obtain 1-(bromomethyl)-2,4-difluoro-5-(2-(methylsulfonyl)propan-2-yl)benzene (367.0 mg, 66%) as a white solid.

[0295] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.60 (t, 1H, J=8.5 Hz), 6.88 (dd, 1H, J=12.4, 9.2 Hz), 4.28 (s, 2H), 2.74 (s, 3H), 1.93 (d, 6H, J=2.6 Hz)

(e) Synthesis of 2,4-difluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde

[0296] 1-(Bromomethyl)-2,4-di fluoro-5-(2-(methylsulfonyppropan-2-yl)benzene (367.0 mg, 1.12 mmol) was dissolved in anhydrous CH.sub.3CN (11.0 mL), and 4-methylmorpholine N-oxide (263.0 mg, 2.24 mmol) and molecular sieves (1.0 g) were added. The reaction mixture was stirred at room temperature for 90 minutes, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was recrystallized with CH.sub.2Cl.sub.2 and n-Hex to obtain 2,4-difluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (200.0 mg, 66%) as a white solid.

[0297] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.16 (s, 1H), 8.07 (t, 1H, J=8.6 Hz), 7.56 (dd, 1H, J=12.6, 10.6 Hz), 2.90 (s, 3H), 1.87 (d, 6H, J=2.5 Hz)

(f) Synthesis of methyl 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate

[0298] 2,4-Difluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (170.0 mg, 0.65 mmol) was dissolved in anhydrous DMF (11.0 mL), and methyl 2-mercaptoacetate (58.0 μL, 0.65 mmol) and K.sub.2CO.sub.3 (179.6 mg, 1.30 mmol) were added. The reaction mixture was stirred at 80° C. for 5 hours, cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain methyl 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (165.0 mg, 77%) as a white solid.

[0299] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.08 (d, 1H, J=7.6 Hz), 8.03 (s, 1H), 7.60 (d, 1H, J=12.8 Hz), 3.96 (s, 3H), 2.77 (s, 3H), 2.00 (d, 6H, J=2.6 Hz)

(g) Synthesis of 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

[0300] Methyl 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (165.0 mg, 0.50 mmol) was dissolved in THF (3.4 mL) and H.sub.2O (1.6 mL), and LiOH.H.sub.2O (210.0 mg, 4.99 mmol) was added. The reaction mixture was stirred at room temperature for 1 hour, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was recrystallized with CH.sub.2Cl.sub.2 and n-Hex to obtain 6-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (150.0 mg, quant) as a white solid.

[0301] LC/MS ESI (−): 315 (M−1)

Intermediate 2) Synthesis of 5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of methyl 5-methylbenzo[b]thiophene-2-carboxylate

[0302] The synthesis procedure of Intermediate 1-f was repeated except for using 2-fluoro-5-methylbenzaldehyde (300.0 mg, 2.17 mmol) as a starting material to obtain methyl 5-methylbenzo[b]thiophene-2-carboxylate (164.0 mg, 37%).

[0303] LC/MS (ESI+): 207 (M+1)

[0304] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.99 (s, 1H), 7.29 (d, 1H, J=8.4 Hz), 7.67 (s, 1H), 7.30 (dd, 1H, J=8.3, 1.3 Hz), 3.94 (s, 3H), 2.48 (s, 3H)

(b) Synthesis of methyl 5-(bromomethyl)benzo[b]thiophene-2-carboxylate

[0305] The synthesis procedure of Intermediate 1-d was repeated except for using methyl 5-methylbenzo[b]thiophene-2-carboxylate (100.0 mg, 0.49 mmol) as a starting material to obtain methyl 5-(bromomethyl)benzo[b]thiophene-2-carboxylate (46.5 mg, 34%).

[0306] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.04 (s, 1H), 7.89 (s, 1H), 7.85 (d, 1H, J=8.4 Hz), 7.50 (d, 1H, J=8.5 Hz), 4.63 (s, 2H), 3.95 (s, 3H)

[0307] The synthesis procedure of Intermediate 1-b was repeated except for using methyl 5-(bromomethyl)benzo[b]thiophene-2-carboxylate (45.0 mg, 0.16 mmol) as a starting material to obtain methyl 5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylate (45.0 mg, quant).

[0308] LC/MS (ESI+): 285 (M+1)

[0309] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.07 (s, 1H), 7.91-7.93 (m, 2H), 7.51 (d, 1H, J=8.4 Hz), 4.37 (s, 2H), 3.96 (s, 3H), 2.80 (s, 3H)

(d) Synthesis of 5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

[0310] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylate (45.0 mg, 0.16 mmol) as a starting material to obtain 5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid (39.3 mg, 90%).

[0311] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.50 (brs, 1H), 8.15 (s, 1H), 8.08 (d, 1H, J=8.5 Hz), 8.03 (s, 1H), 7.53 (d, 1H, J=8.5 Hz), 4.62 (s, 2H), 2.94 (s, 3H)

Intermediate 3) Synthesis of 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of methyl 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylate

[0312] Methyl 5-(bromomethyl)benzo[b]thiophene-2-carboxylate (263.0 mg, 0.92 mmol) and sodium triflinate (216.0 mg, 1.38 mmol) were dissolved in propionitrile (4.6 mL). The reaction mixture was refluxed for 16 hours and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=4:1) to obtain methyl 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylate (171.8 mg, 55%) as a white solid.

[0313] LC/MS (ESI+): 339 (M+1)

[0314] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.08 (s, 1H), 7.94-7.96 (m, 2H), 7.49 (dd, 1H, J=8.5, 1.6 Hz), 4.61 (s, 2H), 3.97 (s, 3H)

(b) Synthesis of 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

[0315] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylate (210.0 mg, 0.62 mmol) as a starting material to obtain 5-(((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid (151.8 mg) without purification.

[0316] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.62 (brs, 1H), 8.20 (s, 1H), 8.15 (d, 1H, J=8.5 Hz), 8.12 (s, 1H), 7.58 (dd, 1H, J=8.5, 1.6 Hz), 5.41 (s, 2H)

Intermediate 4) Synthesis of 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 2-methyl-4-((methylsulfonyl)methyl)-1-nitrobenzene

[0317] The synthesis procedure of Intermediate 1-b was repeated except for using 4-(bromomethyl)-2-methyl-1-nitrobenzene (2.0 g, 8.69 mmol) as a starting material to obtain 2-methyl-4-((methylsulfonyl)methyl)-1-nitrobenzene (1.7 g, 86%).

[0318] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.02 (d, 1H, J=8.1 Hz), 7.40-7.42 (m, 2H), 4.29 (s, 2H), 2.86 (s, 3H), 2.64 (s, 3H)

(b) Synthesis of 4-(fluoro(methylsulfonyl)methyl)-2-methyl-1-nitrobenzene

[0319] 2-Methyl-4-((methylsulfonyl)methyl)-1-nitrobenzene (760.0 mg, 3.32 mmol) and N-fluoro-N-(phenylsulfonyl)benzene sulfonamide (2.1 g, 6.64 mmol) were dissolved in anhydrous THF (16.6 mL), and 1.6M solution of n-BuLi in n-Hex (4.2 mL, 6.64 mmol) was slowly added dropwise at −78° C. The reaction mixture was stirred for 9 hours, H.sub.2O was added at room temperature, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain 4-(fluoro(methylsulfonyl)methyl)-2-methyl-1-nitrobenzene (175.0 mg, 21%) as a brown solid.

[0320] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.05 (d, 1H, J=8.9 Hz), 7.94 (m, 1H), 7.54 (m, 1H), 6.09 (d, 1H, J=46.8 Hz), 3.04 (d, 3H, J=1.6 Hz), 2.65 (s, 3H)

[0321] The synthesis procedure of Intermediate 1-d was repeated except for using 4-(fluoro(methylsulfonyl)methyl)-2-methyl-1-nitrobenzene (168.0 mg, 0.68 mmol) as a starting material to obtain 2-(bromomethyl)-4-(fluoro(methylsulfonyl)methyl)-1-nitrobenzene (129.5 mg).

[0322] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.05 (d, 1H, J=8.9 Hz), 7.95 (m, 1H), 7.93 (m, 1H), 6.10 (d, 1H, J=46.8 Hz), 4.84 (s, 2H), 2.65 (s, 3H)

(d) Synthesis of 5-(fluoro(methylsulfonyl)methyl)-2-nitrobenzaldehyde

[0323] The synthesis procedure of Intermediate 1-e was repeated except for using 2-(bromomethyl)-4-(fluoro(methylsulfonyl)methyl)-1-nitrobenzene (127.0 mg) as a starting material to obtain 5-(fluoro(methylsulfonyl)methyl)-2-nitrobenzaldehyde (13.5 mg, 2 steps yield: 8%).

[0324] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.44 (s, 1H), 8.23 (d, 1H, J=8.5 Hz), 8.13 (d, 1H, J=1.9 Hz), 7.97 (dd, 1H, J=8.5, 2.0 Hz), 6.21 (d, 1H, J=47.0 Hz), 3.10 (d, 3H, J=1.7 Hz)

(e) Synthesis of methyl 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylate

[0325] The synthesis procedure of Intermediate 1-f was repeated except for using 5-(fluoro(methylsulfonyl)methyl)-2-nitrobenzaldehyde (10.0 mg, 0.04 mmol) as a starting material to obtain methyl 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylate (11.0 mg, quant).

[0326] LC/MS (ESI+): 303 (M+1)

[0327] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.11 (s, 1H), 8.08 (s, 1H), 7.98 (d, 1H, J=8.6 Hz), 7.63 (dd, 1H, J=8.5, 1.6 Hz), 6.17 (d, 1H, J=46.2 Hz), 3.97 (s, 3H), 3.02 (d, 3H, J=1.4 Hz)

(f) Synthesis of 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid

[0328] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylate (11.0 mg, 0.04 mmol) as a starting material to obtain 5-(fluoro(methylsulfonyl)methyl)benzo[b]thiophene-2-carboxylic acid (6.7 mg, 64%).

[0329] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 8.23 (s, 1H), 8.17-8.20 (m, 2H), 7.59 (dd, 1H, J=8.5, 1.6 Hz), 6.93 (d, 1H, J=45.2 Hz), 3.19 (d, 3H, J=1.2 Hz)

Intermediate 5) Synthesis of 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 2-methyl-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene

[0330] The synthesis procedure of Intermediate 1-c was repeated except for using 2-methyl-4-((methylsulfonyl)methyl)-1-nitrobenzene (500.0 mg, 2.18 mmol) as a starting material to obtain 2-methyl-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene (308.0 mg, 55%).

[0331] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.00 (d, 1H, J=9.2 Hz), 7.62-7.63 (m, 2H), 2.65 (s, 3H), 2.61 (s, 3H), 1.88 (s, 6H)

(b) Synthesis of 2-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene

[0332] The synthesis procedure of Intermediate 1-d was repeated except for using 2-methyl-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene (270.0 mg, 1.05 mmol) as a starting material to obtain 2-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene (272.0 mg).

[0333] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.07 (d, 1H, J=8.7 Hz), 7.84 (d, 1H, J=2.2 Hz), 7.77 (dd, 1H, J=8.7, 2.2 Hz), 4.86 (s, 2H), 2.63 (s, 3H), 1.91 (s, 6H)

[0334] The synthesis procedure of Intermediate 1-e was repeated except for using 2-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)-1-nitrobenzene (270.0 mg) as a starting material to obtain 5-(2-(methylsulfonyl)propan-2-yl)-2-nitrobenzaldehyde (139.0 mg, 2 step yield: 49%).

[0335] LC/MS (ESI+): 272 (M+1)

[0336] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.46 (s, 1H), 8.10-8.18 (m, 3H), 2.66 (s, 3H), 1.93 (s, 6H)

(d) Synthesis of methyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate

[0337] The synthesis procedure of Intermediate 1-f was repeated except for using 5-(2-(methylsulfonyl)propan-2-yl)-2-nitrobenzaldehyde (137.0 mg, 0.51 mmol) as a starting material to obtain methyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (140.0 mg, 89%).

[0338] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.12 (d, 1H, J=1.8 Hz), 8.08 (s, 1H), 7.90 (d, 1H, J=8.7 Hz), 7.79 (dd, 1H, J=8.7, 1.9 Hz), 3.96 (s, 3H), 2.55 (s, 3H), 1.93 (s, 6H)

(e) Synthesis of 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

[0339] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (155.0 mg, 0.50 mmol) as a starting material to obtain 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (115.0 mg, 78%).

[0340] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.55 (brs, 1H), 8.25 (s, 1H), 8.14 (s, 1H), 8.07 (d, 1H, J=8.7 Hz), 7.76 (dd, 1H, J=8.8, 1.7 Hz), 2.73 (s, 3H), 1.83 (s, 6H)

Intermediate 6) Synthesis of 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 2-methyl-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene

[0341] 2-Methyl-4-((methylsulfonyl)methyl)-1-nitrobenzene (500.0 mg, 2.18 mmol), 1,2-dibromoethane (0.3 mL, 3.27 mmol) and tetra-n-butylammonium bromide (70.3 mg, 0.22 mmol) were dissolved in toluene (22.0 mL), and 10N NaOH aqueous solution (0.7 mL, 6.54 mmol) was slowly added. The reaction mixture was heated at 40° C. for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=4:1) to obtain 2-methyl-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene (92.0 mg, 17%) as a yellow oil.

[0342] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.00 (d, 1H, J=8.4 Hz), 7.58 (m, 1H), 7.53 (m, 1H), 2.79 (s, 3H), 2.62 (s, 3H), 1.89-1.92 (m, 2H), 1.30-1.33 (m, 2H)

(b) Synthesis of 2-(bromomethyl)-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene

[0343] The synthesis procedure of Intermediate 1-d was repeated except for using 2-methyl-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene (95.0 mg, 0.37 mmol) as a starting material to obtain 2-(bromomethyl)-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene (102.0 mg).

[0344] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.05 (d, 1H, J=8.4 Hz), 7.79 (d, 1H, J=2.0 Hz), 7.69 (dd, 1H, J=8.4, 2.0 Hz), 4.83 (s, 2H), 2.80 (s, 3H), 1.90-1.95 (m, 2H), 1.34-1.37 (m, 2H)

[0345] The synthesis procedure of Intermediate 1-e was repeated except for using 2-(bromomethyl)-4-(1-(methylsulfonyl)cyclopropyl)-1-nitrobenzene (100.0 mg) as a starting material to obtain 5-(1-(methylsulfonyl)cyclopropyl)-2-nitrobenzaldehyde (40.6 mg, 2 steps yield: 41%).

[0346] LC/MS (ESI+): 270 (M+1)

[0347] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.43 (s, 1H), 8.16 (d, 1H, J=8.2 Hz), 8.03-8.07 (m, 2H), 2.80 (s, 3H), 1.96-1.99 (m, 2H), 1.35-1.39 (m, 2H)

(d) Synthesis of methyl 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylate

[0348] The synthesis procedure of Intermediate 1-f was repeated except for using 5-(1-(methylsulfonyl)cyclopropyl)-2-nitrobenzaldehyde (40.0 mg, 0.15 mmol) as a starting material to obtain methyl 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylate (35.9 mg, 78%).

[0349] LC/MS (ESI+): 311 (M+1)

[0350] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.04-8.07 (m, 2H), 7.88 (m, 1H), 7.67 (m, 1H), 3.96 (s, 3H), 2.77 (s, 3H), 1.90-1.91 (m, 2H), 1.34-1.36 (m, 2H)

(e) Synthesis of 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylic acid

[0351] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylate (33.0 mg, 0.11 mmol) as a starting material to obtain 5-(1-(methylsulfonyl)cyclopropyl)benzo[b]thiophene-2-carboxylic acid (21.9 mg, 70%).

[0352] LC/MS ESI (+): 297 (M+1)

[0353] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.57 (brs, 1H), 8.19 (s, 1H), 8.10 (s, 1H), 8.07 (d, 1H, J=8.5 Hz), 7.67 (d, 1H, J=8.9 Hz), 2.88 (s, 3H), 1.67-1.70 (m, 2H), 1.35-1.38 (m, 2H)

Intermediate 7) Synthesis of 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 1-(2-chloro-4-fluoro-5-methylphenyl)ethan-1-one

[0354] AlCl.sub.3 (5.8 g, 43.3 mmol) was dissolved in 1,2-dichloroethane (34.6 mL), and acetyl chloride (3.1 mL, 43.3 mmol) was added dropwise at 0° C. 4-Chloro-2-fluoro-1-methylbenzene (5.0 g, 34.6 mmol) was added. The reaction mixture was stirred at 0° C. for 1 hour and then at 60° C. for 16 hours. 1N HCl aqueous solution was added dropwise, and the reaction mixture was extracted with EtOAc. The organic extract was washed with sat. NaHCO.sub.3 aqueous solution and brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 1-(2-chloro-4-fluoro-5-methylphenyl)ethan-1-one (4.9 g, 75%) as a yellow oil.

[0355] LC/MS ESI (+): 187 (M+1)

[0356] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.48 (d, 1H, J=8.1 Hz), 7.10 (d, 1H, J=9.1 Hz), 2.64 (s, 3H), 2.27 (s, 3H)

(b) Synthesis of 2-(2-chloro-4-fluoro-5-methylphenyl)propan-2-ol

[0357] 1-(2-Chloro-4-fluoro-5-methylphenyl)ethan-1-one (4.9 g, 26.00 mmol) was dissolved in THF (260.0 mL), and 3.0M solution of methylmagnesium bromide in Et.sub.2O (26.0 mL) was added dropwise at −8° C. The reaction mixture was stirred for 16 hours, 1N HCl aqueous solution was added dropwise at 0° C. to quench the reaction, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=2:1) to obtain 2-(2-chloro-4-fluoro-5-methylphenyl)propan-2-ol (4.3 g, 82%) as a colorless oil.

[0358] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.50 (d, 1H, J=8.4 Hz), 7.04 (d, 1H, J=9.1 Hz), 2.44 (s, 1H), 2.25 (d, 3H, J=1.7 Hz), 1.70 (s, 6H)

[0359] 2-(2-Chloro-4-fluoro-5-methylphenyl)propan-2-ol (4.3 g, 21.40 mmol) and Lawesson's reagent (5.2 g, 12.80 mmol) were dissolved in toluene (107.0 mL), and H.sub.2O (0.5 mL) was added. The reaction mixture was stirred at 50° C. for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with sat. NaHCO.sub.3 aqueous solution, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:DCM=4:1) to obtain 2-(2-chloro-4-fluoro-5-methylphenyl)propane-2-thiol (2.7 g, 59%) as a pale yellow oil.

[0360] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.31 (d, 1H, J=8.1 Hz), 7.08 (d, 1H, J=9.1 Hz), 2.89 (s, 1H), 2.24 (s, 3H), 1.92 (s, 6H)

(d) Synthesis of (2-(2-chloro-4-fluoro-5-methylphenyl)propan-2-yl)(methyl)sulfane

[0361] NaOH (357.0 mg, 8.92 mmol) was dissolved in EtOH (34.3 mL), and dimethyl sulfate (1.0 mL, 10.29 mmol) was added dropwise. 2-(2-Chloro-4-fluoro-5-methylphenyl)propane-2-thiol (1.5 g, 6.86 mmol) was added, and the reaction mixture was stirred at room temperature for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:DCM=6:1) to obtain (2-(2-chloro-4-fluoro-5-methylphenyl)propan-2-yl)(methyl)sulfane (1.5 g, 93%) as a colorless oil.

[0362] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.27 (d, 1H, J=7.7 Hz), 7.08 (d, 1H, J=9.2 Hz), 2.25 (d, 3H, J=1.7 Hz), 1.81-1.83 (m, 9H)

(e) Synthesis of 1-chloro-5-fluoro-4-methyl-2-(2-(methylsulfonyl)propan-2-yl)benzene

[0363] (2-(2-Chloro-4-fluoro-5-methylphenyl)propan-2-yl)(methyl)sulfane (1.5 g, 6.36 mmol) was dissolved in AcOH (31.8 mL) and 35 wt % H.sub.2O.sub.2 aqueous solution (6.4 mL) was added dropwise. The reaction mixture was stirred at room temperature for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with sat. NaHCO.sub.3 aqueous solution and brine, dried over anhydrous Na.sub.2SO and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=4:1) to obtain 1-chloro-5-fluoro-4-methyl-2-(2-(methylsulfonyl)propan-2-yl)benzene (1.6 g, 95%) as a white solid.

[0364] LC/MS ESI (+): 265 (M+1)

[0365] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.55 (d, 1H, J=8.1 Hz), 7.09 (d, 1H, J=9.0 Hz), 2.76 (s, 3H), 2.27 (s, 3H), 2.03 (s, 6H)

(f) Synthesis of 1-(bromomethyl)-4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzene

[0366] The synthesis procedure of Intermediate 1-d was repeated except for using 1-chloro-5-fluoro-4-methyl-2-(2-(methylsulfonyl)propan-2-yl)benzene (1.7 g, 6.35 mmol) as a starting material to obtain 1-(bromomethyl)-4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzene (2.2 g).

[0367] LC/MS ESI (+): 343 (M+1)

[0368] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.77 (d, 1H, J=7.9 Hz), 7.18 (d, 1H, J=9.1 Hz), 4.47 (s, 2H), 2.77 (s, 3H), 2.06 (s, 6H)

(g) Synthesis of 4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde

[0369] The synthesis procedure of Intermediate 1-e was repeated except for using 1-(bromomethyl)-4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzene (2.2 g) as a starting material to obtain 4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (1.0 g, 2 step yield: 57%).

[0370] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.29 (s, 1H), 8.22 (d, 1H, J=7.4 Hz), 7.34 (d, 1H, J=9.6 Hz), 2.78 (s, 3H), 2.09 (s, 6H)

(h) Synthesis of methyl 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate

[0371] The synthesis procedure of Intermediate 1-f was repeated except for using 4-chloro-2-fluoro-5-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (1.0 g, 3.59 mmol) as a starting material to obtain methyl 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (1.1 g, 91%).

[0372] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.27 (s, 1H), 8.03 (s, 1H), 7.94 (s, 1H), 3.96 (s, 3H), 2.79 (s, 3H), 2.14 (s, 6H)

(i) Synthesis of 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

[0373] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (1.1 g, 3.26 mmol) as a starting material to obtain 6-chloro-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (998.0 mg, 92%).

[0374] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.67 (brs, 1H), 8.44 (s, 1H), 8.26 (s, 1H), 8.14 (s, 1H), 2.88 (s, 3H), 2.04 (s, 6H)

Intermediate 8) Synthesis of 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-C]pyridine-2-carboxylic acid

(a) Synthesis of 2-(bromomethyl)-4-methyl-5-nitropyridine

[0375] The synthesis procedure of Intermediate 1-d was repeated except for using 2,4-dimethyl-5-nitropyridine (2.5 g, 16.43 mmol) as a starting material to obtain 2-(bromomethyl)-4-methyl-5-nitropyridine (1.1 g, 28%).

[0376] LC/MS ESI (+): 231 (M+1)

[0377] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.11 (s, 1H), 7.74 (s, 1H), 4.75 (s, 2H), 2.59 (s, 3H)

(b) Synthesis of 4-methyl-2-((methylsulfonyl)methyl)-5-nitropyridine

[0378] The synthesis procedure of Intermediate 1-b was repeated except for using 2-(bromomethyl)-4-methyl-5-nitropyridine (1.1 g, 4.76 mmol) as a starting material to obtain 4-methyl-2-((methylsulfonyl)methyl)-5-nitropyridine (980.0 mg, 89%).

[0379] LC/MS ESI (+): 231 (M+1)

[0380] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.15 (s, 1H) 7.50 (s, 1H), 4.46 (s, 2H), 2.98 (s, 3H), 2.69 (s, 3H)

[0381] 4-Methyl-2-((methylsulfonyl)methyl)-5-nitropyridine (980.0 mg, 4.25 mmol) was dissolved in anhydrous DMF (21.2 mL), and 60 wt % NaH (426.0 mg, 10.64 mmol) and CH.sub.3I (0.8 mL, 12.75 mmol) were added at 0° C. The reaction mixture was stirred at room temperature for 16 hours, H.sub.2O was added at 0° C., and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=2:1) to obtain 4-methyl-2-(2-(methylsulfonyl)propan-2-yl)-5-nitropyridine (290.0 mg, 26%) as a white solid.

[0382] LC/MS ESI (+): 259 (M+1)

[0383] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.14 (s, 1H) 7.65 (s, 1H), 2.82 (s, 3H), 2.69 (s, 3H), 1.92 (s, 6H)

(d) Synthesis of (E)-N,N-dimethyl-2-(2-(2-(methylsulfonyl)propan-2-yl)-5-nitropyridin-4-yl)ethene-1-amine

[0384] 4-Methyl-2-(2-(methylsulfonyl)propan-2-yl)-5-nitropyridine (250.0 mg, 0.97 mmol) was dissolved in anhydrous DMF (1.2 mL) and N,N-dimethylformamide dimethylacetal (1.3 mL, 9.68 mmol) was added. The reaction mixture was stirred for 1 hour, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain (E)-N,N-dimethyl-2-(2-(2-(methylsulfonyl)propan-2-yl)-5-nitropyridin-4-yl)ethene-1-amine (250.0 mg, 82%) as a red solid.

[0385] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.93 (s, 1H) 7.58 (s, 1H), 7.35 (d, 1H, J=13.2 Hz), 5.98 (d, 1H, J=13.2 Hz), 3.05 (s, 6H), 2.95 (s, 3H), 1.87 (s, 6H)

(e) Synthesis of 2-(2-(methylsulfonyl)propan-2-yl)-5-nitroisonicotinaldehyde

[0386] (E)-N,N-dimethyl-2-(2-(2-(methylsulfonyl)propan-2-yl)-5-nitropyridin-4-yl)ethene-1-amine (250.0 mg, 0.80 mmol) was dissolved in THF (4.0 mL) and H.sub.2O (4.0 mL), and sodium metaperiodate (512.0 mg, 2.39 mmol) was added. The reaction mixture was stirred at 40° C. for 5 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain 2-(2-(methylsulfonyl)propan-2-yl)-5-nitroisonicotinaldehyde (130.0 mg, 60%) as a yellow solid.

[0387] LC/MS ESI (+): 273 (M+1)

[0388] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.55 (s, 1H) 9.41 (s, 1H), 8.06 (s, 1H), 2.87 (s, 3H), 1.95 (s, 6H)

(f) Synthesis of methyl 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxylate

[0389] The synthesis procedure of Intermediate 1-f was repeated except for using 2-(2-(methylsulfonyl)propan-2-yl)-5-nitroisonicotinaldehyde (130.0 mg, 0.48 mmol) as a starting material to obtain methyl 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxylate (110.0 mg, 74%).

[0390] LC/MS ESI (+): 314 (M+1)

[0391] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 9.16 (s, 1H) 8.10 (s, 1H), 8.07 (s, 1H), 4.00 (s, 3H), 2.82 (s, 3H), 1.98 (s, 6H)

(g) Synthesis of 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxylic acid

[0392] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxylate (110.0 mg, 7.64 mmol) as a starting material to obtain 5-(2-(methylsulfonyl)propan-2-yl)thieno[2,3-c]pyridine-2-carboxylic acid (100.0 mg, 95%).

[0393] LC/MS ESI (+): 300 (M+1)

[0394] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 9.37 (s, 1H) 8.28 (s, 1H), 8.16 (s, 1H), 2.86 (s, 3H), 1.86 (s, 6H)

Intermediate 9) Synthesis of 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 2-fluoro-1-methyl-4-((methylsulfonyl)methyl)benzene

[0395] The synthesis procedure of Intermediate 1-b was repeated except for using 4-(bromomethyl)-2-fluoro-1-methylbenzene (1.0 g, 4.92 mmol) as a starting material to obtain 2-fluoro-1-methyl-4-((methylsulfonyl)methyl)benzene (813.0 mg, 82%).

[0396] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.23 (t, 1H, J=8.1 Hz), 7.07-7.10 (m, 2H), 4.20 (s, 2H), 2.78 (s, 3H), 2.29 (s, 3H)

(b) Synthesis of 2-fluoro-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene

[0397] The synthesis procedure of Intermediate 1-c was repeated except for using 2-fluoro-1-methyl-4-((methylsulfonyl)methyl)benzene (813.0 mg, 4.02 mmol) as a starting material to obtain 2-fluoro-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (620 mg, 67%).

[0398] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.26-7.32 (m, 2H), 7.21 (t, 1H, J=8.4 Hz), 2.54 (s, 3H), 2.28 (s, 3H), 1.82 (s, 6H)

[0399] The synthesis procedure of Intermediate 1-d was repeated except for using 2-fluoro-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (620.0 mg, 2.69 mmol) to obtain 1-(bromomethyl)-2-fluoro-4-(2-(methylsulfonyl)propan-2-yl)benzene (680.0 mg, 79%).

[0400] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.35-7.46 (m, 3H), 4.51 (s, 2H), 2.58 (s, 3H), 1.84 (s, 6H)

(d) Synthesis of 2-fluoro-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde

[0401] The synthesis procedure of Intermediate 1-e was repeated except for using 1-(bromomethyl)-2-fluoro-4-(2-(methylsulfonyl)propan-2-yl)benzene (650.0 mg, 2.10 mmol) as a starting material to obtain 2-fluoro-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (330.0 mg, 64%).

[0402] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.23 (s, 1H), 7.88 (t, 1H, J=8.3 Hz), 7.60-7.64 (m, 2H), 2.78 (s, 3H), 1.78 (s, 6H)

(e) Synthesis of methyl 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate

[0403] The synthesis procedure of Intermediate 1-f was repeated except for using 2-fluoro-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (350.0 mg, 1.43 mmol) as a starting material to obtain methyl 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (265.0 mg, 59%).

[0404] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.33 (s, 1H), 8.22 (s, 1H), 8.04 (d, 1H, J=8.6 Hz), 7.73 (dd, 1H, J=8.6, 1.7 Hz), 3.90 (s, 3H), 2.74 (s, 3H), 1.84 (s, 6H)

(f) Synthesis of 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

[0405] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (265.0 mg, 0.85 mmol) as a starting material to obtain 6-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (230.0 mg, 91%).

[0406] LC/MS ESI (−): 297 (M−1)

Intermediate 10) Synthesis of 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-ol

[0407] 4-Bromo-1-fluoro-2-methylbenzene (1.0 g, 5.29 mmol) was dissolved in anhydrous THF (26.0 mL), and 1.6M solution of n-BuLi in THF (3.5 mL, 5.55 mmol) and tetrahydro-4H-pyran-4-one (556.0 mg, 5.55 mmol) were added at −78° C. The reaction mixture was stirred at 0° C. for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-ol (800.0 mg, 72%) as a white solid.

[0408] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.31 (dd, 1H, J=7.3, 2.2 Hz), 7.26 (m, 1H), 6.99 (t, 1H, J=8.9 Hz), 3.84-3.98 (m, 4H), 2.29 (s, 3H), 2.08-2.18 (m, 2H), 1.65-1.69 (m, 3H)

(b) Synthesis of 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-thiol

[0409] The synthesis procedure of Intermediate 7-c was repeated except for using 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-ol (800.0 mg, 3.80 mmol) as a starting material to obtain 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-thiol (450.0 mg, 52%).

[0410] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ, 7.40 (dd, 1H, J=7.4, 2.4 Hz), 7.32 (m, 1H), 7.10 (t, 1H, J=8.9 Hz), 3.76-3.82 (m, 2H), 3.65-3.69 (m, 2H), 3.26 (s, 1H), 2.24 (s, 3H), 2.08-2.18 (m, 4H)

[0411] The synthesis procedure of Intermediate 7-d was repeated except for using 4-(4-fluoro-3-methylphenyl)tetrahydro-2H-pyran-4-thiol (450.0 g, 1.99 mmol) as a starting material to obtain 4-(4-fluoro-3-methylphenyl)-4-(methylthio)tetrahydro-2H-pyran (300.0 mg, 63%).

[0412] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 7.33 (d, 1H, J=7.4 Hz), 7.25 (m, 1H), 7.09 (t, 1H, J=9.0 Hz), 3.77-3.82 (m, 2H), 3.57-3.62 (m, 2H), 2.24 (s, 3H), 2.04-2.12 (m, 4H), 1.60 (s, 3H)

(d) Synthesis of 4-(4-fluoro-3-methylphenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran

[0413] The synthesis procedure of Intermediate 7-e was repeated except for using 4-(4-fluoro-3-methylphenyl)-4-(methylthio)tetrahydro-2H-pyran (300.0 mg, 1.25 mmol) as a starting material to obtain 4-(4-fluoro-3-methylphenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran (300.0 mg, 89%).

[0414] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.39 (dd, 1H, J=7.0, 2.4 Hz), 7.33 (m, 1H), 7.10 (t, 1H, J=8.8 Hz), 3.98-4.02 (m, 2H), 3.40 (t, 2H, J=11.7 Hz), 2.55-2.63 (m, 2H), 2.42-2.47 (m, 5H), 2.33 (s, 3H)

(e) Synthesis of 4-(3-(bromomethyl)-4-fluorophenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran

[0415] The synthesis procedure of Intermediate 1-d was repeated except for using 4-(4-fluoro-3-methylphenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran (300.0 mg, 1.10 mmol) as a starting material to obtain 4-(3-(bromomethyl)-4-fluorophenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran (340.0 mg, 88%).

[0416] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.59 (dd, 1H, J=6.9, 2.6 Hz), 7.50 (m, 1H), 7.19 (t, 1H, J=8.9 Hz), 4.54 (s, 2H), 3.98-4.02 (m, 2H), 3.36-3.42 (m, 2H), 2.55-2.65 (m, 2H), 2.42-2.50 (m, 5H)

(f) Synthesis of 2-fluoro-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzaldehyde

[0417] The synthesis procedure of Intermediate 1-e was repeated except for using 4-(3-(bromomethyl)-4-fluorophenyl)-4-(methylsulfonyl)tetrahydro-2H-pyran (350.0 mg, 1.00 mmol) as a starting material to obtain 2-fluoro-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzaldehyde (220.0 mg, 76%).

[0418] LC/MS ESI (−): 285 (M−1)

(g) Synthesis of methyl 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylate

[0419] The synthesis procedure of Intermediate 1-f was repeated except for using 2-fluoro-5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzaldehyde (110.0 mg, 0.38 mmol) as a starting material to obtain methyl 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylate (124.0 mg, 91%).

[0420] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ, 8.06-8.09 (m, 2H), 7.97 (d, 1H, J=8.7 Hz), 7.66 (dd, 1H, J=8.7, 1.9 Hz), 4.03-4.06 (m, 2H), 3.97 (s, 3H), 3.43 (t, 2H, J=11.6 Hz), 2.56-2.72 (m, 4H), 2.49 (s, 3H)

(h) Synthesis of 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylic acid

[0421] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylate (124.0 mg, 0.35 mmol) as a starting material to obtain 5-(4-(methylsulfonyl)tetrahydro-2H-pyran-4-yl)benzo[b]thiophene-2-carboxylic acid (104.0 mg, 87%).

[0422] LC/MS ESI (−): 339 (M−1)

Intermediate 11) Synthesis of 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylic acid

(a) Synthesis of 2-(3-bromo-4-methylphenyl)propan-2-ol

[0423] The synthesis procedure of Intermediate 7-b was repeated except for using 1-(3-bromo-4-methylphenyl)ethan-1-one (1.0 g, 4.69 mmol) as a starting material to obtain 2-(3-bromo-4-methylphenyl)propan-2-ol (1.0 g, 96%).

[0424] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.67 (d, 1H, J=1.8 Hz), 7.31 (dd, 1H, J=7.9, 1.8 Hz), 7.20 (d, 1H, J=7.9 Hz), 2.38 (s, 3H), 1.70 (s, 1H), 1.56 (s, 6H)

(b) Synthesis of 2-(3-bromo-4-methylphenyl)propane-2-thiol

[0425] The synthesis procedure of Intermediate 7-c was repeated except for using 2-(3-bromo-4-methylphenyl)propan-2-ol (1.0 g, 4.50 mmol) as a starting material to obtain 2-(3-bromo-4-methylphenyl)propane-2-thiol (1.0 g, 92%).

[0426] .sup.1H-NMR (400 MHz, CDCl.sub.3): 0.5-7.71 (s, 1H), 7.40 (d, 1H, J=8.0 Hz), 7.18 (d, 1H, J=8.0 Hz), 2.37 (s, 3H), 2.24 (s, 1H), 1.79 (s, 6H)

[0427] The synthesis procedure of Intermediate 7-d was repeated except for using 2-(3-bromo-4-methylphenyl)propane-2-thiol (1.0 g, 4.08 mmol) as a starting material to obtain (2-(3-bromo-4-methylphenyl)propan-2-yl)(methyl)sulfane (872.7 mg, 83%).

[0428] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.65 (d, 1H, J=2.0 Hz), 7.36 (dd, 1H, J=8.0, 2.0 Hz), 7.18 (d, 1H, J=8.0 Hz), 2.37 (s, 3H), 1.79 (s, 3H), 1.66 (s, 6H)

(d) Synthesis of 2-bromo-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene

[0429] The synthesis procedure of Intermediate 7-e was repeated except for using (2-(3-bromo-4-methylphenyl)propan-2-yl)(methyl)sulfane (871.0 mg, 3.36 mmol) as a starting material to obtain 2-bromo-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (973.7 mg, quant).

[0430] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.76 (s, 1H), 7.51 (d, 1H, J=8.1 Hz), 7.27 (d, 1H, J=8.1 Hz), 2.56 (s, 3H), 2.41 (s, 3H), 1.82 (s, 6H)

(e) Synthesis of 2-bromo-1-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)benzene

[0431] The synthesis procedure of Intermediate 1-d was repeated except for using 2-bromo-1-methyl-4-(2-(methylsulfonyl)propan-2-yl)benzene (972.0 mg, 3.34 mmol) as a starting material to obtain 2-bromo-1-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)benzene (894.4 mg, 72%).

[0432] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.82 (d, 1H, J=2.0 Hz), 7.61 (dd, 1H, J=8.2, 2.0 Hz), 7.50 (d, 1H, J=8.2 Hz), 4.59 (s, 2H), 2.59 (s, 3H), 1.84 (s, 6H)

(f) Synthesis of 2-bromo-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde

[0433] The synthesis procedure of Intermediate 1-e was repeated except for using 2-bromo-1-(bromomethyl)-4-(2-(methylsulfonyl)propan-2-yl)benzene (890.0 mg, 2.41 mmol) as a starting material to obtain 2-bromo-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (475.9 mg, 65%).

[0434] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.36 (s, 1H), 7.94 (d, 1H, J=8.3 Hz), 7.92 (d, 1H, J=1.8 Hz), 7.74 (dd, 1H, J=8.3, 1.2 Hz), 2.62 (s, 3H), 1.88 (s, 6H)

(g) Synthesis of methyl (Z)-2-(((benzyloxy)carbonyl)amino)-3-(2-bromo-4-(2-(methylsulfonyl)propan-2-yl)phenyl)acrylate

[0435] 2-Bromo-4-(2-(methylsulfonyl)propan-2-yl)benzaldehyde (441.0 mg, 1.45 mmol), methyl 2-(((benzyloxy)carbonyl)amino)-2-(dimethoxyphosphoryl)acetate (622.0 mg, 1.88 mmol) and DBU (330.0 mg, 2.17 mmol) were dissolved in CH.sub.2Cl.sub.2 (14.5 mL). The reaction mixture was stirred at room temperature for 30 minutes, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:1) to obtain methyl (Z)-2-(((benzyloxy)carbonyl)amino)-3-(2-bromo-4-(2-(methylsulfonyl)propan-2-yl)phenyl)acrylate (570.0 mg, 77%).

[0436] LC/MS ESI (+): 510 (M+1)

[0437] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.82 (s, 1H), 7.51 (s, 2H), 7.32-7.37 (m, 4H), 7.26-7.29 (m, 2H), 6.55 (brs, 1H), 5.04 (s, 2H), 3.87 (s, 3H), 2.53 (s, 3H), 1.82 (s, 6H)

(h) Synthesis of methyl 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylate

[0438] Methyl (Z)-2-(((benzyloxy)carbonyl)amino)-3-(2-bromo-4-(2-(methylsulfonyl)propan-2-yl)phenyl)acrylate (570.0 mg, 1.12 mmol), CuI (42.5 mg, 0.22 mmol), L-proline (51.4 mg, 0.45 mmol) and K.sub.2CO.sub.3 (463.0 mg, 3.35 mmol) were dissolved in 1,4-dioxane (5.6 mL). The reaction mixture was stirred at 100° C. for 2 days, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:1) to obtain methyl 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylate (227.0 mg, 69%).

[0439] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 12.02 (s, 1H), 7.67-7.69 (m, 2H), 7.37 (dd, 1H, J=8.6, 1.8 Hz), 7.16 (d, 1H, J=1.5 Hz), 3.88 (s, 3H), 2.68 (s, 3H), 1.80 (s, 6H)

(i) Synthesis of 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylic acid hydrochloride

[0440] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylate (227.0 mg, 0.77 mmol) as a starting material to obtain 6-(2-(methylsulfonyl)propan-2-yl)-1H-indole-2-carboxylic acid hydrochloride (170.0 mg, 79%).

[0441] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.02 (brs, 1H), 11.82 (s, 1H), 7.64-7.67 (m, 2H), 7.35 (dd, 1H, J=8.8, 1.6 Hz), 7.07 (d, 1H, J=1.6 Hz), 2.67 (s, 3H), 1.80 (s, 6H)

Intermediate 12) Synthesis of 5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of 2-(4-fluoro-3-methylphenyl)propan-2-ol

[0442] The synthesis procedure of Intermediate 7-b was repeated except for using 1-(4-fluoro-3-methylphenyl)ethan-1-one (1.0 g, 6.57 mmol) as a starting material to obtain 2-(4-fluoro-3-methylphenyl)propan-2-ol (872.0 mg, 79%).

[0443] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.31 (dd, 1H, J=7.4, 2.1 Hz), 7.25 (m, 1H), 6.95 (t, 1H, J=8.9 Hz), 2.28 (s, 3H), 1.71 (s, 1H), 1.57 (s, 6H)

(b) Synthesis of 2-(4-fluoro-3-methylphenyl)propane-2-thiol

[0444] The synthesis procedure of Intermediate 7-c was repeated except for using 2-(4-fluoro-3-methylphenyl)propan-2-ol (872.0 mg, 5.18 mmol) as a starting material to obtain 2-(4-fluoro-3-methylphenyl)propane-2-thiol (955.0 mg, 85%).

[0445] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.37 (dd, 1H, J=7.1, 2.3 Hz), 7.32 (m, 1H), 6.93 (t, 1H, J=8.9 Hz), 2.28 (s, 3H), 2.24 (s, 1H), 1.81 (s, 6H)

[0446] 2-(4-Fluoro-3-methylphenyl)propane-2-thiol (400.0 mg, 2.17 mmol) was dissolved in anhydrous DMF (16.3 mL), and 1-bromo-2-methoxyethane (392.0 mg, 2.82 mmol) and Cs.sub.2CO.sub.3 (1.4 g, 4.34 mmol) were added. The reaction mixture was stirred at 70° C. for 5 hours, cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain (2-(4-fluoro-3-methylphenyl)propan-2-yl)(2-methoxyethyl)sulfane (420.0 mg, 80%) as a white solid.

[0447] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.34 (dd, 1H, J=7.4, 2.3 Hz), 7.29 (m, 1H), 6.92 (t, 1H, J=8.9 Hz), 3.32 (t, 2H, J=6.7 Hz), 3.26 (s, 3H), 2.43 (t, 2H, J=6.7 Hz), 2.27 (s, 3H), 1.68 (s, 6H)

(d) Synthesis of 1-fluoro-4-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)-2-methylbenzene

[0448] The synthesis procedure of Intermediate 7-e was repeated except for using (2-(4-fluoro-3-methylphenyl)propan-2-yl)(2-methoxyethyl)sulfane (420.0 mg, 1.73 mmol) as a starting material to obtain 1-fluoro-4-(24(2-methoxyethyl)sulfonyl)propan-2-yl)-2-methylbenzene (410.0 mg, 86%).

[0449] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.32-7.40 (m, 2H), 7.02 (t, 1H, J=8.9 Hz), 3.64 (t, 2H, J=6.7 Hz), 3.29 (s, 3H), 2.91 (t, 2H, J=6.7 Hz), 2.30 (s, 3H), 1.82 (s, 6H) (e) Synthesis of 2-(bromomethyl)-1-fluoro-4-(24(2-methoxyethyl)sulfonyl)propan-2-yl)benzene

[0450] The synthesis procedure of Intermediate 1-d was repeated except for using 1-fluoro-4-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)-2-methylbenzene (410.0 mg, 1.49 mmol) as a starting material to to obtain 2-(bromomethyl)-1-fluoro-4-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzene (40.0 mg, 8%).

[0451] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.65 (dd, 1H, J=7.0, 2.6 Hz), 7.58 (m, 1H), 7.10 (t, 1H, J=9.0 Hz), 4.52 (s, 2H), 3.64 (t, 2H, J=6.5 Hz), 3.29 (s, 3H), 2.93 (t, 2H, J=6.5 Hz), 1.84 (s, 6H)

(f) Synthesis of 2-fluoro-5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzaldehyde

[0452] The synthesis procedure of Intermediate 1-e was repeated except for using 2-(bromomethyl)-1-fluoro-4-(2-(2-methoxyethyl)sulfonyl)propan-2-yl)benzene (60.0 mg, 0.17 mmol) as a starting material to obtain 2-fluoro-5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzaldehyde (36.0 mg, 74%).

[0453] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.30 (s, 1H), 7.99 (dd, 1H, J=6.4, 2.7 Hz), 7.93 (m, 1H), 7.17 (t, 1H, J=9.2 Hz), 3.62 (t, 2H, J=6.4 Hz), 3.23 (s, 3H), 2.87 (t, 2H, J=6.4 Hz), 1.80 (s, 6H)

(g) Synthesis of methyl 5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate

[0454] The synthesis procedure of Intermediate 1-f was repeated except for using 2-fluoro-5-(2-(2-methoxyethyl)sulfonyl)propan-2-yl)benzaldehyde (36.0 mg, 0.13 mmol) as a starting material to obtain methyl 5-(2-(2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (30.0 mg, 67%).

[0455] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.10 (s, 1H), 8.07 (s, 1H), 7.90 (d, 1H, J=8.7 Hz), 7.78 (dd, 1H, J=8.7, 2.0 Hz), 3.96 (s, 3H), 3.63 (t, 2H, J=6.4 Hz), 3.25 (s, 3H), 2.91 (t, 2H, J=6.4 Hz), 1.93 (s, 6H)

(h) Synthesis of 5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid

[0456] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(2-((2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylate (30.0 mg, 0.08 mmol) as a starting material to obtain 5-(2-(2-methoxyethyl)sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (27.0 mg, 94%).

[0457] LC/MS ESI (−): 341 (M−1)

Intermediate 13) Synthesis of 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of (4-fluoro-3-methylbenzyl)(methyl)sulfane

[0458] 4-(Bromomethyl)-1-fluoro-2-methylbenzene (1.0 g, 4.92 mmol) and sodium methanethiolate (380.0 mg, 5.42 mmol) were dissolved in DMF (24.6 mL). The reaction mixture was stirred at room temperature for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:CH.sub.2Cl.sub.2=4:1) to obtain (4-fluoro-3-methylbenzyl)(methyl)sulfane (709.0 mg, 85%) as a colorless liquid.

[0459] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.12 (d, 1H, J=7.3 Hz), 7.06 (m, 1H), 6.93 (m, 1H), 3.61 (s, 2H), 2.26 (s, 3H), 1.99 (s, 3H)

(b) Synthesis of (E)-N-((4-fluoro-3-methylbenzyl)(methyl)-λ.SUP.4.-sulfanylidene)-4-nitrobenzenesulfonamide

[0460] (4-Fluoro-3-methylbenzyl)(methyl)sulfane (600.0 mg, 3.52 mmol), 4-nitrobenzenesulfonamide (869.0 mg, 4.39 mmol) and (diacetoxyiodo)benzene (1.7 g, 5.37 mmol) were dissolved in CH.sub.3CN (35.8 mL). The reaction mixture was stirred at 90° C. for 16 hours, cooled to room temperature, and concentrated under reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, CH.sub.3CN:H.sub.2O) to obtain (E)-N-((4-fluoro-3-methylbenzyl)(methyl)-λ.sup.4-sulfanylidene)-4-nitrobenzenesulfonamide (606.0 mg, 46%).

[0461] LC/MS ESI (+): 371 (M+1)

[0462] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.18 (d, 2H, J=8.9 Hz), 7.88 (d, 2H, J=8.9 Hz), 7.01-7.05 (m, 2H), 6.91 (m, 1H), 4.16 (d, 1H, J=12.8 Hz), 4.07 (d, 1H, J=12.8 Hz), 2.66 (s, 3H), 2.20 (d, 3H, J=1.9 Hz)

[0463] (E)-N-((4-fluoro-3-methylbenzyl)(methyl)-λ.sup.4-sulfanylidene)-4-nitrobenzene sulfonamide (600.0 mg, 1.62 mmol), RuCl.sub.3H.sub.2O (36.5 mg, 0.16 mmol) and NaIa.sub.4 (520.0 mg, 2.43 mmol) were dissolved in a mixture of CH.sub.2Cl.sub.2/H.sub.2O (16.3 mL, 10/3 v/v). The reaction mixture was stirred at room temperature for 16 hours, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:2) to obtain N-((4-fluoro-3-methylbenzyl)(methyl)(oxo)-λ.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (546.0 mg, 87%).

[0464] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.32 (d, 2H, J=9.0 Hz), 8.14 (d, 2H, J=9.0 Hz), 7.30 (dd, 1H, J=6.9, 1.9 Hz), 7.25 (m, 1H), 7.08 (m, 1H), 4.69 (s, 2H), 3.09 (s, 3H), 2.31 (d, 3H, J=1.8 Hz)

(d) Synthesis of N-((3-(bromomethyl)-4-fluorobenzyl)(methyl)(oxo)-λ.SUP.6.-sulfanylidene)-4-nitrobenzene sulfonamide

[0465] The synthesis procedure of Intermediate 1-d was repeated except for using N-((4-fluoro-3-methylbenzyl)(methyl)(oxo)-λ.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (546.0 mg, 1.41 mmol) as a starting material to obtain N-((3-(bromomethyl)-4-fluorobenzyl)(methyl)(oxo)-?.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (657.0 mg, quant).

[0466] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.32 (d, 2H, J=9.0 Hz), 8.13 (d, 2H, J=9.0 Hz), 7.52 (m, 1H), 7.43 (m, 1H), 7.17 (m, 1H), 4.72 (s, 2H), 4.51 (s, 2H), 3.13 (s, 3H)

(e) Synthesis of N-((4-fluoro-3-formylbenzyl)(methyl)(oxo)-λ.SUP.6.-sulfanylidene)-4-nitrobenzene sulfonamide

[0467] The synthesis procedure of Intermediate 1-e was repeated except for using N-((3-(bromomethyl)-4-fluorobenzyl)(methyl)(oxo)-λ.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (657.0 mg, 1.41 mmol) as a starting material to obtain N-((4-fluoro-3-formylbenzyl)(methyl)(oxo)-λ.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (357.7 mg, 63%).

[0468] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 10.38 (s, 1H), 8.33 (d, 2H, J=8.8 Hz), 8.14 (d, 2H, J=8.8 Hz), 7.92 (dd, 1H, J=6.2, 2.4 Hz), 7.82-7.86 (m, 1H), 7.34 (m, 1H), 4.75-4.83 (m, 2H), 3.14 (s, 3H)

(f) Synthesis of methyl 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylate

[0469] The synthesis procedure of Intermediate 1-f was repeated except for using N-((4-fluoro-3-formylbenzyl)(methyl)(oxo)-λ.sup.6-sulfanylidene)-4-nitrobenzene sulfonamide (306.0 mg, 0.77 mmol) as a starting material to obtain methyl 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylate (139.0 mg, 65%).

[0470] LC/MS ESI (+): 284 (M+1)

[0471] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.08 (s, 1H), 7.91-7.93 (m, 2H), 7.51 (dd, 1H, J=8.5, 1.7 Hz), 4.52 (d, 1H, J=13.1 Hz), 4.36 (d, 1H, J=13.1 Hz), 3.97 (s, 3H), 3.77 (s, 1H), 2.97 (s, 3H)

(g) Synthesis of 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylic acid

[0472] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylate (137.0 mg, 0.48 mmol) as a starting material to obtain 5-((S-methylsulfonimidoyl)methyl)benzo[b]thiophene-2-carboxylic acid (93.4 mg, 46%).

[0473] LC/MS ESI (+): 270 (M+1)

[0474] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 8.13 (s, 1H), 8.06 (d, 1H, J=8.3 Hz), 8.04 (s, 1H), 7.57 (dd, 1H, J=8.4, 1.4 Hz), 4.55-4.57 (m, 3H), 2.86 (d, 3H, J=3.5 Hz)

Intermediate 14) Synthesis of 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of methyl 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylate

[0475] Tetrahydrothiophene 1,1-dioxide (124.0 mg, 1.03 mmol) was dissolved in anhydrous THF (7.3 mL), and 1M solution of lithium bis(trimethylsilyl)amide in THF (1.5 mL, 1.55 mmol) was added dropwise at −20° C. The reaction mixture was stirred at room temperature for 30 minutes, and ZnCl.sub.2 (211.0 mg, 1.55 mmol) was added −20° C. The reaction mixture was slowly warmed to room temperature, methyl 5-bromobenzo[b]thiophene-2-carboxylate (200.0 mg, 0.74 mmol), Pd(OAc).sub.2 (8.3 mg, 0.04 mmol) and XPhos (35.2 mg, 0.07 mmol) were added, and stirred at 65° C. for 5 hours. The reaction mixture was cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain methyl 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylate (60.0 mg, 26%) as an off-white solid.

[0476] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.06 (s, 1H), 7.89-7.91 (m, 2H), 7.49 (dd, 1H, J=8.4, 2.0 Hz), 4.30 (m, 1H), 3.95 (s, 3H), 2.95-3.35 (m, 3H), 2.22-2.58 (m, 3H)

(b) Synthesis of 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylic acid

[0477] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylate (70.0 mg, 0.23 mmol) as a starting material to obtain 5-(1,1-dioxidotetrahydrothiophen-2-yl)benzo[b]thiophene-2-carboxylic acid (60.0 mg, 90%) as a white solid.

[0478] LC/MS ESI (−): 295 (M−1)

[0479] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 13.55 (s, 1H), 8.13 (s, 1H), 8.08 (d, 1H, J=8.5 Hz), 8.02 (s, 1H), 7.51 (d, 1H, J=8.4 Hz), 4.50 (m, 1H), 3.17-3.36 (m, 2H), 2.38-2.46 (m, 2H), 2.13-2.28 (m, 2H)

Intermediate 15) Synthesis of 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylic acid

(a) Synthesis of methyl 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylate

[0480] The synthesis procedure of Intermediate 14-a was repeated except for using methyl 5-bromobenzo[b]thiophene-2-carboxylate (95.0 mg, 0.35 mmol) and tetrahydro-2H-thiopyrane 1,1-dioxide (66.0 mg, 0.49 mmol) as a starting material to obtain methyl 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylate (26.0 mg, 23%) as an off-white solid.

[0481] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.06 (s, 1H), 7.95 (s, 1H), 7.89 (d, 1H, J=8.5 Hz), 7.53 (d, 1H, J=8.5 Hz), 4.15 (m, 1H), 3.95 (s, 3H), 3.09-3.29 (m, 2H), 1.56-2.59 (m, 6H)

(b) Synthesis of 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylic acid

[0482] The synthesis procedure of Intermediate 1-g was repeated except for using methyl 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylate (26.0 mg, 0.08 mmol) as a starting material to obtain 5-(1,1-dioxidotetrahydro-2H-thiopyran-2-yl)benzo[b]thiophene-2-carboxylic acid (22.0 mg, 88%) as a white solid.

[0483] LC/MS ESI (−): 309 (M−1)

Example 1) Synthesis of N-(3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 3-chloro-5-nitrobenzoyl chloride

[0484] 3-Chloro-5-nitrobenzoic acid (5.0 g, 24.81 mmol) was dissolved in SOCl.sub.2 (10.0 mL, 137.00 mmol), and a catalytic amount of anhydrous DMF was added. The reaction mixture was refluxed at 110° C. for 2 hours and concentrated under reduced pressure to obtain 3-chloro-5-nitrobenzoyl chloride (5.3 g, quant.) as a yellow liquid without purification.

(b) Synthesis of (3-chloro-5-nitrophenyl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone

[0485] 3-Chloro-5-nitrobenzoyl chloride (5.0 g, 22.70 mmol) was dissolved in anhydrous Et.sub.2O (230.0 mL), and (3-methoxy-5-(trifluoromethoxy)phenyl)boronic acid (5.4 g, 22.70 mmol), Pd(dba).sub.2 (1.3 g, 2.27 mmol), PPh.sub.3 (1.2 g, 4.54 mmol) and copper thiophene-2-carboxylate (4.3 g, 22.70 mmol) were added. The reaction mixture was stirred at room temperature for 15 hours, filtered through Celite, and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=9:1) to obtain (3-chloro-5-nitrophenyl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone (4.2 g, 41%) as a yellow oil.

[0486] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.49 (s, 1H), 8.46 (s, 1H), 8.10 (s, 1H), 7.26 (s, 1H), 7.18 (s, 1H), 7.05 (s, 1H), 3.90 (s, 3H)

[0487] (3-Chloro-5-nitrophenyl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone (4.0 g, 10.65 mmol) was dissolved in 1,2-dibromoethane (106.0 mL) and PCl.sub.5 (11.1 g, 53.24 mmol) was added. The reaction mixture was stirred at 110° C. for 24 hours and cooled to room temperature. The reaction mixture was poured into a solution of NaHCO.sub.3 in ice water, vigorously stirred, and extracted with CH.sub.2Cl.sub.2. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=20:1) to obtain 1-chloro-3-(dichloro(3-methoxy-5-(trifluoromethoxy)phenyl)methyl)-5-nitrobenzene (1.4 g, 30%) as a yellow oil.

[0488] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.37 (s, 1H), 8.24 (s, 1H), 7.91 (s, 1H), 7.08 (s, 1H), 7.05 (s, 1H), 6.81 (s, 1H), 3.84 (s, 3H)

(d) Synthesis of 1-chloro-3-(2-(3-methoxy-5-(tri fluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene

[0489] 1M solution of TiCl.sub.4 in CH.sub.2Cl.sub.2 (0.6 mL, 0.63 mmol) was added to 1.2M solution of dimethylzinc in toluene (7.8 mL, 9.41 mmol) at −40° C., and stirred for 1 hour. 1-Chloro-3-(dichloro(3-methoxy-5-(trifluoromethoxy)phenyl)methyl)-5-nitrobenzene (1.4 g, 3.14 mmol) in CH.sub.2Cl.sub.2 (11.4 mL) was slowly added dropwise at −40° C., and the reaction mixture was warmed to 0° C. and stirred for 18 hours. H.sub.2O was added, and the reaction mixture was extracted with CH.sub.2Cl.sub.2. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=9:1) to obtain 1-chloro-3-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene (750.0 mg, 61%) as a yellow solid.

[0490] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.07 (s, 1H), 8.00 (s, 1H), 7.48 (s, 1H), 6.62-6.65 (m, 3H), 3.78 (s, 3H), 1.70 (s, 6H)

(e) Synthesis of 3-(2-(3-chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenol

[0491] 1-Chloro-3-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene (450.0 mg, 1.15 mmol) was dissolved in anhydrous CH.sub.2Cl.sub.2 (8.0 mL) and 1M solution of BBr.sub.3 in CH.sub.2Cl.sub.2 (3.5 mL, 3.46 mmol) was slowly added dropwise at 0° C. The reaction mixture was stirred at room temperature for 8 hours, H.sub.2O was added at 0° C., and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=3:1) to obtain 3-(2-(3-chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenol (380.0 mg, 88%) as a colorless oil.

[0492] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.07 (s, 1H), 8.00 (s, 1H), 7.48 (s, 1H), 6.64 (s, 1H), 6.61 (s, 1H), 6.55 (s, 1H), 5.00 (s, 1H), 1.69 (s, 6H)

(f) Synthesis of 1-chloro-3-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene

[0493] 3-(2-(3-Chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenol (370.0 mg, 0.98 mmol) was dissolved in anhydrous DMF (9.8 mL), and K.sub.2CO.sub.3 (406.0 mg, 2.94 mmol) and iodoethane (158.0 mL, 1.97 mmol) were added. The reaction mixture was stirred at 40° C. for 15 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 1-chloro-3-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene (386.0 mg, 97%) as a colorless oil.

[0494] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.07 (s, 1H), 8.00 (s, 1H), 7.48 (s, 1H), 6.60-6.63 (m, 3H), 3.98 (q, 2H, J=7.0 Hz), 1.69 (s, 6H), 1.40 (t, 3H, J=7.0 Hz)

(g) Synthesis of 3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)aniline

[0495] 1-Chloro-3-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)-5-nitrobenzene (380.0 mg, 0.94 mmol) was dissolved in a mixture of MeOH/H.sub.2O (10.0 mL, 9/1 v/v), and Zn (616.0 mg, 9.43 mmol) and NH.sub.4Cl (504.0 mg, 9.43 mmol) were added at room temperature. The reaction mixture was ultrasonificated at 40° C. for 40 minutes, cooled to room temperature, filtered through Celite, and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:1) to obtain 3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)aniline (350.0 mg, 98%) as a white solid.

[0496] LC/MS ESI (+): 374 (M+1)

(h) Synthesis of N-(3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0497] 5-(2-(Methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (38.8 mg, 0.13 mmol), 3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)aniline (48.6 mg, 0.13 mmol) and HATU (53.0 mg, 0.14 mmol) were dissolved in anhydrous DMF (1.3 mL) and DIPEA (44.0 μL, 0.24 mmol) was added. The reaction mixture was stirred at 40° C. for 3 hours, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain N-(3-chloro-5-(2-(3-ethoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (35.0 mg, 41%) as a white solid.

[0498] LC/MS ESI (+): 654 (M+1)

[0499] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, J=8.8 Hz), 7.88 (s, 1H), 7.74 (d, 1H, J=8.8 Hz), 7.52 (s, 1H), 7.04 (s, 1H), 6.77 (s, 2H), 6.72 (s, 1H), 4.01 (q, 2H, J=6.9 Hz), 2.73 (s, 3H), 1.84 (s, 6H), 1.64 (s, 6H), 1.29 (t, 3H, J=6.9 Hz)

[0500] Compounds from Examples 2 to 16 were synthesized through the synthesis route of Example 1, and data of these compounds are listed as follows.

TABLE-US-00002 TABLE 2 Ex. Compound Analysis data 2 N-(3-chloro-5-(2-(3-propoxy-5- LC/MS ESI (+): 668 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.34 (s, 1H), 8.19 (s, 1H), 8.09 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.88 (s, 1H), 7.74 (d, 1H, J = 8.8 Hz), 7.53 (s, 1H), 7.04 (s, 1H), 6.78 (s, 2H), 6.72 (s, 1H), 3.93 (t, 2H, J = 6.4 Hz), 2.73 (s, 3H), 1.85 (s, 6H), 1.67-1.73 (m, 2H) 1.64 (s, 6H), 0.96 (t, 3H, J = 8.8 Hz) 3 N-(3-(2-(3-methoxy-5- LC/MS ESI (+): 606 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.50 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.35 (s, 1H), 8.19 (s, 1H), 8.09 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.72 (t, 2H, J = 9.6 Hz), 7.63 (s, 1H), 7.31 (t, 1H, J = 8.0 Hz), 7.01 (d, 1H, J = 8.0 Hz), 6.78 (d, 2H, J = 6.4 Hz), 6.70 (s, 1H), 3.75 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H), 1.65 (s, 6H) 4 N-(3-bromo-5-(2-(3-(1,1,2,2- LC/MS ESI (+): 770 (M + 1) tetrafluoroethoxy)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.64 (s, (trifluoromethoxy)phenyl)propan-2- 1H), 8.34 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)phenyl)-5-(2-(methylsulfonyl)propan- J = 8.8 Hz), 8.04 (s, 1H), 7.75 (d, 1H, J = 8.8 Hz), 2-yl)benzo[b]thiophene-2-carboxamide 7.59 (s, 1H), 7.27 (s, 1H), 7.23 (s, 1H), 7.19 (s, 1H), 7.13 (s, 1H), 6.81 (t, 1H, J = 51.9 Hz), 2.73 (s, 3H), 1.85 (s, 6H), 1.68 (s, 6H) 5 N-(3-chloro-5-(2-(3-(1,1,2,2- LC/MS ESI (−): 724 (M − 1) tetrafluoroethoxy)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, (trifluoromethoxy)phenyl)propan-2- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, yl)phenyl)-5-(2-(methylsulfonyl)propan- J = 8.4 Hz), 7.92 (t, 1H, J = 1.6 Hz), 7.75 (dd, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8, 2.0 Hz), 7.56 (s, 1H), 7.28 (s, 1H), 7.24 (s, 1H), 7.14 (s, 1H), 7.08 (s, 1H), 6.81 (tt, 1H, J = 51.6, 3.2 Hz), 2.74 (s, 3H), 1.86 (s, 6H), 1.69 (s, 6H) 6 N-(3-methoxy-5-(2-(3-methoxy-5- LC/MS ESI (+): 636 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.48 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.34 (s, 1H), 8.18 (s, 1H), 8.09 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.73 (d, 1H, J = 8.8 Hz), 7.41 (s, 1H), 7.19 (s, 1H), 6.79 (d, 2H, J = 8.8 Hz), 6.71 (s, 1H), 6.56 (s, 1H), 3.75 (s, 3H), 3.73 (s, 3H) 2.73 (s, 3H), 1.84 (s, 6H), 1.62 (s, 6H) 7 N-(3-chloro-5-(2-(3-methoxy-5- LC/MS ESI (+): 640 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.34 (s, 1H), 8.19 (s, 1H), 8.09 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.88 (s, 1H), 7.74 (d, 1H, J = 8.8 Hz), 7.52 (s, 1H), 7.04 (s, 1H), 6.81 (s, 2H), 6.73 (s, 1H), 3.76 (s, 3H), 2.73 (s, 3H) 1.85 (s, 6H), 1.64 (s, 6H) 8 N-(3-chloro-5-(2-(3-(2- LC/MS ESI (+): 739 (M + 1) morpholinoethoxy)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, (trifluoromethoxy)phenyl)propan-2- 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.10 (d, 1H, yl)phenyl)-5-(2-(methylsulfonyl)propan- J = 8.7 Hz), 7.89 (s, 1H), 7.74 (d, 1H, J = 8.7 Hz), 2-yl)benzo[b]thiophene-2-carboxamide 7.54 (s, 1H), 7.05 (s, 1H), 6.83 (s, 1H), 6.79 (s, 1H), 6.74 (s, 1H), 4.07-4.10 (m, 2H), 3.54-3.55 (m, 4H), 2.73 (s, 3H), 2.43-2.64 (m, 6H), 1.85 (s, 6H), 1.64 (s, 6H) 9 N-(3-bromo-5-(2-(3-isopropoxy-5- LC/MS ESI (+): 712 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.61 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 8.03 (s, 1H), 7.74 (d, 1H, J = 8.6 Hz), 7.59 (s, 1H), 7.17 (s, 1H), 6.77 (s, 1H), 6.73 (s, 1H), 6.71 (s, 1H), 4.65 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H), 1.64 (s, 6H), 1.24 (d, 6H, J = 6.0 Hz) 10 N-(3-(2-(3-(but-2-yn-1-yloxy)-5- LC/MS ESI (−): 676 (M − 1) (trifluoromethoxy)phenyl)propan-2-yl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, chlorophenyl)-5-(2- 1H), 8.36 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, (methylsulfonyl)propan-2- J = 8.4 Hz), 7.91 (t, 1H, J = 2.0 Hz), 7.75 (dd, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8, 2.0 Hz), 7.55 (s, 1H), 7.06 (s, 1H), 6.85 (s, 1H), 6.84 (s, 1H), 6.80 (s, 1H), 4.78 (s, 2H), 2.75 (s, 3H), 1.86 (s, 6H), 1.80 (s, 3H), 1.66 (s, 6H) 11 N-(3-chloro-5-(2-(3-isobutoxy-5- LC/MS ESI (−): 680 (M − 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.90 (s, 1H), 7.74 (dd, 1H, J = 8.8, 2.0 Hz), 7.54 (s, 1H), 7.06 (s, 1H), 6.82 (s, 1H), 6.80 (s, 1H), 6.73 (s, 1H), 3.76 (d, 2H, J = 6.4 Hz), 2.74 (s, 3H), 1.99 (m, 1H), 1.86 (s, 6H), 1.66 (s, 6H), 0.97 (d, 6H, J = 6.8 Hz) 12 N-(3-chloro-5-(2-(3-(2,2,2- LC/MS ESI (−): 706 (M − 1) trifluoroethoxy)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, (trifluoromethoxy)phenyl)propan-2- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, yl)phenyl)-5-(2-(methylsulfonyl)propan- J = 8.8 Hz), 7.90 (s, 1H), 7.75 (dd, 1H, J = 8.8, 2-yl)benzo[b]thiophene-2-carboxamide 2.0 Hz), 7.55 (s, 1H), 7.06 (s, 1H), 7.00 (s, 1H), 6.98 (s, 1H), 6.85 (s, 1H), 4.82-4.88 (m, 2H), 2.75 (s, 3H), 1.86 (s, 6H), 1.67 (s, 6H) 13 N-(3-chloro-5-(2-(3-(2,2-difluoroethoxy)- LC/MS ESI (−): 688 (M − 1) 5-(trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.90 (s, 1H), 7.75 (dd, 1H, J = 8.8, 1.6 Hz), 7.55 (s, 1H), 7.06 (s, 1H), 6.94 (s, 1H), 6.91 (s, 1H), 6.81 (s, 1H), 6.38 (tt, 1H, J = 54.4, 3.6 Hz), 4.38 (td, 2H, J = 14.4, 3.6 Hz), 2.74 (s, 3H), 1.86 (s, 6H), 1.67 (s, 6H) 14 N-(3-(2-(3-(allyloxy)-5- LC/MS ESI (−): 664 (M − 1) (trifluoromethoxy)phenyl)propan-2-yl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, chlorophenyl)-5-(2- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, (methylsulfonyl)propan-2- J = 8.4 Hz), 7.90 (s, 1H), 7.75 (d, 1H, J = 8.8 Hz), yl)benzo[b]thiophene-2-carboxamide 7.54 (s, 1H), 7.05 (s, 1H), 6.84 (s, 1H), 6.83 (s, 1H), 6.76 (s, 1H), 6.00 (m, 1H), 5.37 (d, 1H, J = 18.0 Hz), 5.27 (d, 1H, J = 9.6 Hz), 4.60 (d, 2H, J = 5.2 Hz), 2.74 (s, 3H), 1.84 (s, 6H), 1.66 (s, 6H) 15 N-(3-chloro-5-(2-(3-cyclopropoxy-5- LC/MS ESI (−): 664 (M − 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, yl)phenyl)-5-(2-(methylsulfonyl)propan- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.11 (d, 1H, 2-yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.91 (s, 1H), 7.75 (d, 1H, J = 8.8 Hz), 7.55 (s, 1H), 7.07 (s, 1H), 6.95 (s, 1H), 6.87 (s, 1H), 6.79 (s, 1H), 3.89 (s, 1H), 2.74 (s, 3H), 1.86 (s, 6H), 1.66 (s, 6H), 0.65-0.79 (m, 4H) 16 N-(3-chloro-5-(2-(3-isopropoxy-5- LC/MS ESI (+): 640 (M + 1) (trifluoromethoxy)phenyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.61 (s, yl)phenyl)-5- 1H), 8.35 (s, 1H), 8.10 (d, 1H, J = 8.4 Hz), ((methylsulfonyl)methyl)benzo[b]thiophene- 8.03 (s, 1H), 7.91 (m, 1H), 7.51-7.54 (m, 2H), 2-carboxamide 7.05 (s, 1H), 6.77 (s, 1H), 6.73 (m, 1H), 6.72 (s, 1H), 4.60-4.66 (m, 3H), 2.93 (s, 3H), 1.64 (s, 6H), 1.24 (d, 6H, J = 6.0 Hz)

Example 17) Synthesis of N-(3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 1-chloro-3-(2-(4-methoxyphenyl)propan-2-yl)-5-nitrobenzene

[0501] 1-(2-Bromopropan-2-yl)-3-chloro-5-nitrobenzene (30.0 mg, 0.11 mmol) and anisole (0.1 mL, 1.07 mmol) were dissolved in 1,2-dichloroethane (1.1 mL) and AlCl.sub.3 (44.0 mg, 0.33 mmol) was added. The reaction mixture was stirred at room temperature for 12 hours, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 1-chloro-3-(2-(4-methoxyphenyl)propan-2-yl)-5-nitrobenzene (40.0 mg, 90%) as a yellow solid.

[0502] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.03 (s, 1H), 8.01 (s, 1H), 7.49 (s, 1H), 7.11 (d, 2H, J=8.4 Hz), 6.84 (d, 2H, J=8.6 Hz), 3.81 (s, 3H), 1.70 (s, 6H)

(b) Synthesis of 3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)aniline

[0503] The synthesis procedure of Example 1-g was repeated except for using 1-chloro-3-(2-(4-methoxyphenyl)propan-2-yl)-5-nitrobenzene (84.2 mg, 0.24 mmol) as a starting material to obtain 3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)aniline (20.0 mg, 56%).

[0504] LC/MS ESI (+): 276 (M+1)

[0505] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.14 (d, 2H, J=8.4 Hz), 6.81 (d, 2H, J=8.6 Hz), 6.64 (s, 1H), 6.49 (s, 1H), 6.36 (s, 1H), 3.79 (s, 3H), 3.62 (s, 2H), 1.59 (s, 6H)

(c) Synthesis of N-(3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0506] The synthesis procedure of Example 1-h was repeated except for using 3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)aniline (81.0 mg, 0.27 mmol) as a starting material to obtain N-(3-chloro-5-(2-(4-methoxyphenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (40.0 mg, 27%).

[0507] LC/MS ESI (+): 556 (M+1)

[0508] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.64 (s, 1H), 8.36 (s, 1H), 8.20 (s, 1H), 8.10 (d, 1H, J=8.4 Hz), 7.87 (s, 1H), 7.75 (dd, 1H, J=8.4, 1.6 Hz), 7.54 (s, 1H), 7.17 (d, 2H, J=8.8 Hz), 7.00 (s, 1H), 6.88 (d, 2H, J=8.8 Hz), 3.74 (s, 3H), 2.74 (s, 3H), 1.86 (s, 6H), 1.64 (s, 6H)

[0509] Compounds from Example 18 to Example 36 were synthesized through the synthesis route of Example 17, and data of these compounds are listed as follows.

TABLE-US-00003 TABLE 3 Ex. Compound Analysis data 18 N-(3-chloro-5-(2-(4-fluorophenyl)propan- LC/MS ESI (+): 544 (M + 1) 2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.64 (brs, (methylsulfonyl)propan-2- 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.08 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.87 (s, 1H), 7.73 (d, 1H, J = 8.7 Hz), 7.52 (s, 1H), 7.27-7.30 (m, 2H), 7.11-7.15 (m, 2H), 7.02 (s, 1H), 2.73 (s, 3H), 1.85 (s, 6H), 1.65 (s, 6H) 19 N-(3-chloro-5-(2-(4-fluorophenyl)propan- LC/MS ESI (+): 562 (M + 1) 2-yl)phenyl)-6-fluoro-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.66 (s, (methylsulfonyl)propan-2- 1H), 8.32 (s, 1H), 8.22 (d, 1H, J = 7.7 Hz), yl)benzo[b]thiophene-2-carboxamide 8.02 (d, 1H, J = 13.1 Hz), 7.86 (s, 1H), 7.49 (s, 1H), 7.28 (dd, 2H, J = 8.7, 5.5 Hz), 7.13 (t, 2H, J = 8.8 Hz), 7.03 (s, 1H), 2.88 (s, 3H), 1.92 (s, 6H), 1.64 (s, 6H) 20 N-(3-bromo-5-(2-(4-fluorophenyl)propan- LC/MS ESI (+): 588 (M + 1) 2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.61 (s, (methylsulfonyl)propan-2- 1H), 8.34 (s, 1H), 8.19 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 8.00 (s, 1H), 7.74 (d, 1H, J = 8.8 Hz), 7.56 (s, 1H), 7.26-7.30 (m, 2H), 7.11-7.15 (m, 3H), 2.73 (s, 3H), 1.84 (s, 6H), 1.64 (s, 6H) 21 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 532 (M + 1) 2-yl)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.60 (s, ((methylsulfonyl)methyl)benzo[b]thiophene- 1H), 8.34 (s, 1H), 8.09 (d, 1H, J = 8.4 Hz), 2-carboxamide 8.02 (s, 1H), 7.89 (m, 1H), 7.50-7.53 (m, 2H), 7.37 (d, 2H, J = 8.6 Hz), 7.27 (d, 2H, J = 8.6 Hz), 7.03 (m, 1H), 4.64 (s, 2H), 2.93 (s, 3H), 1.65 (s, 6H) 22 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 560 (M + 1) 2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.63 (s, (methylsulfonyl)propan-2- 1H), 8.33 (s, 1H), 8.19 (m, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.88 (m, 1H), 7.74 (dd, 1H, J = 8.5, 1.6 Hz), 7.50 (m, 1H), 7.37 (d, 2H, J = 8.5 Hz), 7.27 (d, 2H, J = 8.7 Hz), 7.03 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H), 1.64 (s, 6H) 23 6-chloro-N-(3-chloro-5-(2-(4- LC/MS ESI (+): 594 (M + 1) chlorophenyl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.67 (s, (methylsulfonyl)propan-2- 1H), 8.36 (s, 1H), 8.31 (s, 1H), 8.28 (s, 1H), yl)benzo[b]thiophene-2-carboxamide 7.87 (m, 1H), 7.47 (m, 1H), 7.37 (d, 2H, J = 8.7 Hz), 7.27 (d, 2H, J = 8.7 Hz), 7.04 (m, 1H), 2.89 (s, 3H), 2.05 (s, 6H), 1.64 (s, 6H) 24 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 586 (M + 1) 2-yl)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.62 (s, (((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene- 1H), 8.36 (s, 1H), 8.16 (m, 1H), 8.12 (m, 1H), 2-carboxamide 7.89 (m, 1H), 7.56 (m, 1H), 7.50 (m, 1H), 7.37 (d, 2H, J = 8.7 Hz), 7.27 (d, 2H, J = 8.7 Hz), 7.03 (m, 1H), 5.42 (s, 2H), 1.64 (s, 6H) 25 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 550 (M + 1) 2-yl)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.67 (s, (fluoro(methylsulfonyl)methyl)benzo[b]thiophene- 1H), 8.39 (m, 1H), 8.21 (d, 1H, J = 8.8 Hz), 2-carboxamide 8.13 (s, 1H), 7.89 (m, 1H), 7.59 (d, 1H, J = 8.8 Hz), 7.49 (m, 1H), 7.37 (d, 2H, J = 8.7 Hz), 7.27 (d, 2H, J = 8.7 Hz), 7.03 (m, 1H), 6.94 (d, 1H, J = 45.0 Hz), 3.20 (s, 3H), 1.65 (s, 6H) 26 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 561 (M + 1) 2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.83 (s, (methylsulfonyl)propan-2-yl)thieno[2,3- 1H), 9.39 (s, 1H), 8.38 (s, 1H), 8.26 (s, 1H), c]pyridine-2-carboxamide 7.89 (s, 1H), 7.51 (s, 1H), 7.38 (d, 2H, J = 8.4 Hz), 7.28 (d, 2H, J = 8.4 Hz), 7.08 (s, 1H), 2.87 (s, 3H), 1.88 (s, 6H), 1.66 (s, 6H) 27 N-(3-chloro-5-(2-(5-chlorothiophen-2- LC/MS ESI (+): 566 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.68 (s, (methylsulfonyl)propan-2- 1H), 8.35 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.90 (m, 1H), 7.74 (dd, 1H, J = 8.8, 1.9 Hz), 7.63 (m, 1H), 7.13 (m, 1H), 6.99 (d, 1H, J = 3.9 Hz), 6.86 (d, 1H, J = 3.9 Hz), 2.74 (s, 3H), 1.85 (s, 6H), 1.71 (s, 6H) 28 N-(3-chloro-5-(2-(5-isopropylthiophen-2- LC/MS ESI (+): 574 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.67 (s, (methylsulfonyl)propan-2- 1H), 8.37 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.5 Hz), 7.88 (s, 1H), 7.75 (d, 1H, J = 8.7 Hz), 7.67 (s, 1H), 7.09 (s, 1H), 6.75 (d, 1H J = 3.4 Hz), 6.67 (d, 1H J = 3.3 Hz), 3.08 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H), 1.70 (s, 6H), 1.22 (d, 6H, J = 6.8 Hz) 29 N-(3-chloro-5-(2-(5-methoxythiophen-2- LC/MS ESI (+): 562 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, (methylsulfonyl)propan-2- 1H), 8.36 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.6 Hz), 7.87 (s, 1H), 7.76 (d, 1H, J = 8.7 Hz), 7.64 (s, 1H), 7.08 (s, 1H), 6.58 (d, 1H J = 3.8 Hz), 6.10 (d, 1H J = 3.8 Hz), 3.79 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H), 1.66 (d, 6H) 30 N-(3-chloro-5-(2-(2-methoxythiophen-3- LC/MS ESI (+): 562 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.62 (s, (methylsulfonyl)propan-2- 1H), 8.36 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.6 Hz), 7.84 (t, 1H, J = 1.6 Hz), 7.75 (d, 1H, J = 1.6 Hz), 7.55 (s, 1H), 6.97 (d, 1H J = 1.6 Hz), 6.80 (d, 2H J = 2.0 Hz), 3.63 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H), 1.62 (s, 6H) 31 N-(3-chloro-5-(2-(1-methyl-1H-pyrrol-2- LC/MS ESI (+): 529 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.69 (s, (methylsulfonyl)propan-2-yl)benzo[b]thiophene- 1H), 8.35 (s, 1H), 8.19 (s, 1H), 8.09 (d, 1H, 2-carboxamide J = 8.4 Hz), 7.88 (s, 1H), 7.74 (d, 1H, J = 8.8 Hz), 7.50 (s, 1H), 6.80 (s, 1H), 6.62 (d, 1H, J = 1.6 Hz), 6.10 (m, 1H), 5.94 (t, 1H, J = 1.6 Hz), 3.09 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H), 1.61 (s, 6H) 32 N-(3-chloro-5-(2-(4-methylthiophen-2- LC/MS ESI (+): 546 (M + 1) yl)propan-2-yl)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.69 (s, (methylsulfonyl)propan-2- 1H), 8.36 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.88 (s, 1H), 7.74 (dd, 1H, J = 8.4, 1.6 Hz), 7.64 (s, 1H), 7.08 (s, 1H), 6.95 (s, 1H) 6.78 (s, 1H), 2.73 (s, 3H), 2.17 (s, 3H) 1.85 (s, 6H), 1.70 (s, 6H) 33 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 558 (M + 1) 2-yl)phenyl)-5-(1- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, (methylsulfonyl)cyclopropyl)benzo[b]thiophene- 1H), 8.32 (s, 1H), 8.16 (s, 1H), 8.09 (d, 1H, 2-carboxamide J = 8.4 Hz), 7.87 (m, 1H), 7.66 (dd, 1H, J = 8.2, 1.4 Hz), 7.50 (m, 1H), 7.37 (d, 2H, J = 8.6 Hz), 7.27 (d, 2H, J = 8.6 Hz), 7.03 (m, 1H), 2.89 (s, 3H), 1.68-1.71 (m, 2H), 1.64 (s, 6H), 1.37-1.40 (m, 2H) 34 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 602 (M + 1) 2-yl)phenyl)-5-(4- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, (methylsulfonyl)tetrahydro-2H-pyran-4- 1H), 8.33 (s, 1H), 8.25 (s, 1H), 8.15 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.88 (s, 1H), 7.73 (d, in, J = 8.5 Hz), 7.50 (s, 1H), 7.37 (d, 2, J = 8.5 Hz), 7.27 (d, 2H, J = 8.5 Hz), 7.04 (s, 1H), 3.91 (d, 2H, J = 10.8 Hz), 3.20 (t, 2H, J = 11.8 Hz), 2.73 (d, 2H, J = 12.7 Hz), 2.65 (s, 3H), 2.33 (t, 2H, J = 12.0 Hz), 1.64 (s, 6H) 35 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 543 (M + 1) 2-yl)phenyl)-6-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.85 (s, (methylsulfonyl)propan-2-yl)-1H-indole- 1H), 10.34 (s, 1H), 7.95 (m, 1H), 2-carboxamide 7.68-7.70 (m, 2H), 7.55 (m, 1H), 7.35-7.40 (m, 4H), 7.28 (d, 2H, J = 8.7 Hz), 7.00 (m, 1H), 2.68 (s, 3H), 1.81 (s, 6H), 1.65 (s, 6H) 36 N-(3-chloro-5-(2-(4-chlorophenyl)propan- LC/MS ESI (+): 531 (M + 1) 2-yl)phenyl)-5-((S- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.58 (s, methylsulfonimidoyl)methyl)benzo[b]thiophene- 1H), 8.34 (m, 1H), 8.07 (d, 1H, J = 8.4 Hz), 2-carboxamide 8.04 (m, 1H), 7.89 (m, 1H), 7.55 (dd, 1H, J = 8.4, 1.6 Hz), 7.51 (m, 1H), 7.37 (d, 2H, J = 8.7 Hz), 7.27 (d, 2H, J = 8.7 Hz), 7.03 (m, 1H), 4.47-4.56 (m, 3H), 2.80 (s, 3H), 1.65 (s, 6H)

Example 37) Synthesis of N-(3-chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 1-chloro-3-nitro-5-(4-(trifluoromethoxy)phenoxy)benzene

[0510] 1-Bromo-3-chloro-5-nitrobenzene (200.0 mg, 0.84 mmol), 4-(trifluoromethoxy)phenol (220.0 mg, 1.69 mmol), CuI (80.6 mg, 0.42 mmol), N,N-dimethylglycine (87.2 mg, 0.42 mmol) and Cs.sub.2CO.sub.3 (826.9 mg, 2.53 mmol) were dissolved in anhydrous 1,4-dioxane (5.0 mL). The reaction mixture was stirred at 120° C. for 15 hours, cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex) to obtain 1-chloro-3-nitro-5-(4-(trifluoromethoxy)phenoxy)benzene (160.0 mg, 61%) as a yellow oil.

[0511] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.95 (s, 1H), 7.65 (s, 1H), 7.26-7.30 (m, 3H), 7.09 (d, 2H, J=8.8 Hz)

(b) Synthesis of 3-chloro-5-(4-(trifluoromethoxy)phenoxy)aniline

[0512] The synthesis procedure of Example 1-g was repeated except for using 1-chloro-3-nitro-5-(4-(trifluoromethoxy)phenoxy)benzene (160.0 mg, 0.52 mmol) as a starting material to obtain 3-chloro-5-(4-(trifluoromethoxy)phenoxy)aniline (130.0 mg, 79%) as an off-white oil.

[0513] LC/MS ESI (+): 304 (M+1)

[0514] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.31 (d, 2H, J=8.7 Hz), 6.95 (d, 2H, J=8.7 Hz), 6.41 (s, 1H), 6.34 (s, 1H), 6.16 (s, 1H), 3.76 (brs, 2H)

(c) Synthesis of N-(3-chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0515] The synthesis procedure of Example 1-h was repeated except for using 3-chloro-5-(4-(trifluoromethoxy)phenoxy)aniline (130.0 mg, 0.42 mmol) and 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (150.0 mg, 0.55 mmol) as starting materials, to obtain N-(3-chloro-5-(4-(trifluoromethoxy)phenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (75.0 mg, 47%) as a white solid.

[0516] LC/MS ESI (+): 584 (M+1)

[0517] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.74 (brs, 1H), 8.34 (s, 1H), 8.21 (s, 1H), 8.09 (d, 1H, J=8.7 Hz), 7.79 (s, 1H), 7.74 (d, 1H, J=8.7 Hz), 7.46 (d, 2H, J=8.7 Hz), 7.40 (t, 1H, J=1.8 Hz), 7.26 (d, 2H, J=8.9 Hz), 6.96 (t, 1H, J=1.8 Hz), 2.73 (s, 3H), 1.85 (s, 6H)

[0518] Compounds from Example 38 to Example 61 were synthesized through the synthesis route of Example 37, and data of these compounds are listed as follows.

TABLE-US-00004 TABLE 4 Ex. Compound Analysis data 38 N-(3-chloro-5-(4- LC/MS ESI (+): 568 (M + 1) (trifluoromethyl)phenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.77 (s, 1H), (methylsulfonyl)propan-2- 8.34 (s, 1H), 8.21 (d, 1H, J = 1.5 Hz), 8.10 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.82 (s, 1H), 7.81 (d, 2H, J = 8.7 Hz), 7.75 (dd, 1H, J = 8.8, 1.8 Hz), 7.47 (m, 1H), 7.30 (d, 2H, J = 8.5 Hz), 7.05 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 39 N-(3-bromo-5-(4- LC/MS ESI (−): 576 (M − 1) chlorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.69 (s, 1H), (methylsulfonyl)propan-2- 8.34 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.4 Hz), 7.90 (s, 1H), 7.75 (d, 1H, J = 8.4 Hz), 7.52 (d, 2H, J = 8.8 Hz), 7.42 (s, 1H), 7.18 (d, 2H, J = 8.8 Hz), 7.04 (s, 1H), 2.74 (s, 3H), 1.86 (s, 6H) 40 N-(3-chloro-5-(4- LC/MS ESI (+): 517 (M + 1) chlorophenoxy)phenyl)-6-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.90 (s, 1H), (methylsulfonyl)propan-2-yl)-1H- 10.42 (s, 1H), 7.79 (m, 1H), 7.70 (d, 1H, indole-2-carboxamide J = 8.7 Hz), 7.67 (s, 1H), 7.52 (d, 2H, J = 8.9 Hz), 7.45 (m, 1H), 7.40 (m, 1H), 7.36 (dd, 1H, J = 8.7, 1.8 Hz), 7.19 (d, 2H, J = 8.9 Hz), 6.89 (m, 1H), 2.68 (s, 3H), 1.80 (s, 6H) 41 N-(3-chloro-5-(4- LC/MS ESI (+): 506 (M + 1) chlorophenoxy)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.68 (s, 1H), ((methylsulfonyl)methyl)benzo[b]thiophene- 8.33 (s, 1H), 8.09 (d, 1H, J = 8.3 Hz), 8.03 (s, 2-carboxamide 1H), 7.76 (m, 1H), 7.54 (s, 1H), 7.44 (d, 2H, J = 8.8 Hz), 7.36 (m, 1H), 7.18 (d, 2H, J = 8.8 Hz), 6.92 (m, 1H), 4.64 (s, 2H), 2.93 (s, 3H) 42 N-(3-chloro-5-(4- LC/MS ESI (+): 560 (M + 1) chlorophenoxy)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.70 (s, 1H), (((trifluoromethyl)sulfonyl)methyl)benzo[b]thiophene- 8.35 (s, 1H), 8.15-8.18 (m, 2H), 7.75 (m, 1H), 2-carboxamide 7.56 (m, 1H), 7.51 (d, 2H, J = 8.9 Hz), 7.35 (m, 1H), 7.18 (d, 2H, J = 8.9 Hz), 6.92 (m, 1H), 5.41 (s, 2H) 43 N-(3-chloro-5-(4- LC/MS ESI (+): 518 (M + 1) fluorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.72 (brs, (methylsulfonyl)propan-2- 1H), 8.33 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.74-7.76 (m, 2H), 7.30-7.34 (m, 3H), 7.20-7.23 (m, 2H), 6.86 (s, 1H), 2.74 (s, 3H), 1.85 (s, 6H) 44 N-(3-chloro-5-(4- LC/MS ESI (+): 552 (M + 1) chlorophenoxy)phenyl)-6-fluoro-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.74 (s, (methylsulfonyl)propan-2- 1H), 8.31 (s, 1H), 8.24 (d, 1H, J = 7.6 Hz), yl)benzo[b]thiophene-2-carboxamide 8.02 (d, 1H, J = 13.1 Hz), 7.75 (s, 1H), 7.51 (d, 2H, J = 8.6 Hz), 7.34 (s, 1H), 7.18 (d, 2H, J = 8.6 Hz), 6.93 (s, 1H), 2.87 (s, 3H), 1.92 (s, 6H) 45 6-chloro-N-(3-chloro-5-(4- LC/MS ESI (+): 568 (M + 1) chlorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.74 (s, 1H), (methylsulfonyl)propan-2- 8.38 (s, 1H), 8.31 (s, 1H), 8.28 (s, 1H), 7.75 (m, yl)benzo[b]thiophene-2-carboxamide 1H), 7.51 (d, 2H, J = 8.9 Hz), 7.34 (m, 1H), 7.18 (d, 2H, J = 8.9 Hz), 6.93 (m, 1H), 2.89 (s, 3H), 2.05 (s, 6H) 46 N-(3-(4-chlorophenoxy)-5- LC/MS ESI (+): 530 (M + 1) methoxyphenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.53 (brs, (methylsulfonyl)propan-2- 1H), 8.34 (s, 1H), 8.19 (s, 1H), 8.08 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.73 (d, 1H, J = 8.7 Hz), 7.47 (d, 2H, J = 8.7 Hz), 7.30 (s, 1H), 7.11 (d, 2H, J = 8.9 Hz), 7.04 (s, 1H), 6.44 (s, 1H), 3.77 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H) 47 N-(3-chloro-5-(3-chloro-5- LC/MS ESI (+): 552 (M + 1) fluorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6); δ 10.76 (s, 1H), (methylsulfonyl)propan-2- 8.35 (s, 1H), 8.22 (d, 1H, J = 1.6 Hz), 8.10 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.81 (m, 1H), 7.75 (dd, 1H, J = 8.7, 1.8 Hz), 7.44 (m, 1H), 7.32 (dt, 1H, J = 8.6, 2.0 Hz), 7.08-7.12 (m, 2H), 7.03 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 48 N-(3-chloro-5-(3- LC/MS ESI (+): 584 (M + 1) (trifluoromethoxy)phenoxy)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.78 (brs, (2-(methylsulfonyl)propan-2- 1H), 8.34 (s, 1H), 8.22 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.80 (s, 1H), 7.75 (d, 1H, J = 8.8 Hz), 7.59 (t, 1H, J = 8.0 Hz), 7.44 (s, 1H) 7.15-7.26 (m, 3H), 6.98 (s, 1H), 2.74 (s, 3H), 1.86 (s, 6H) 49 N-(3-chloro-5-(4- LC/MS ESI (+): 534 (M + 1) chlorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.70 (s, 1H), (methylsulfonyl)propan-2- 8.32 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.73-7.76 (m, 2H), 7.51 (d, 2H, J = 8.9 Hz), 7.36 (m, 1H), 7.18 (d, 2H, J = 8.9 Hz), 6.91 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 50 N-(3-chloro-5-(4- LC/MS ESI (+): 535 (M + 1) chlorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.91 (brs, (methylsulfonyl)propan-2-yl)thieno[2,3- 1H), 9.38 (s, 1H), 8.36 (s, 1H), 8.27 (s, 1H), c]pyridine-2-carboxamide 7.76 (s, 1H), 7.52 (d, 2H, J = 8.8 Hz), 7.36 (s, 1H), 7.19 (d, 2H, J = 8.8 Hz), 6.96 (s, 1H), 2.87 (s, 3H), 1.87 (s, 6H) 51 N-(3-chloro-5-(3-chloro-4- LC/MS ESI (+): 552 (M + 1) fluorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.71 (brs, (methylsulfonyl)propan-2- 1H), 8.34 (s, 1H), 8.21 (d, 1H, J = 1.6 Hz), yl)benzo[b]thiophene-2-carboxamide 8.10 (d, 1H, J = 8.7 Hz), 7.73-7.77 (m, 2H), 7.49-7.54 (m, 2H), 7.34 (m, 1H), 7.20 (m, 1H), 6.93 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 52 N-(3-chloro-5-(3,4- LC/MS ESI (+): 536 (M + 1) difluorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.70 (s, 1H), (methylsulfonyl)propan-2- 8.34 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.73-7.77 (m, 2H), 7.55 (m, 1H), 7.42 (m, 1H), 7.36 (m, 1H), 7.04 (m, 1H), 6.93 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 53 N-(3-chloro-5-(3-fluoro-5- LC/MS ESI (+): 548 (M + 1) methoxyphenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.75 (s, 1H), (methylsulfonyl)propan-2- 8.35 (s, 1H), 8.21 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.73-7.78 (m, 2H), 7.40 (s, 1H), 6.96 (s, 1H), 6.73 (m, 1H), 6.57-6.61 (m, 2H), 3.78 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H) 54 N-(3-chloro-5-(4-chloro-3- LC/MS ESI (+): 552 (M + 1) fluorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.72 (s, 1H), (methylsulfonyl)propan-2- 8.34 (s, 1H), 8.21 (d, 1H, J = 1.4 Hz), 8.10 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.79 (m, 1H), 7.75 (dd, 1H, J = 8.8, 1.8 Hz), 7.66 (t, 1H, J = 8.7 Hz), 7.41 (m, 1H), 7.35 (dd, 1H, J = 10.4, 2.7 Hz), 6.99-7.04 (m, 2H), 2.73 (s, 3H), 1.85 (s, 6H) 55 N-(3-chloro-5-(2-(3-chloro-5- LC/MS ESI (+): 564 (M + 1) methoxyphenyl)propan-2-yl)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.71 (s, 1H), (2-(methylsulfonyl)propan-2- 8.34 (s, 1H), 8.20 (d, 1H, J = 1.6 Hz), 8.09 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.79 (t, 1H, J = 1.8H), 7.74 (dd, 1H, J = 8.7, 1.8 Hz), 7.39 (t, 1H, J = 1.9H), 6.96 (t, 1H, J = 1.9H), 6.91 (t, 1H, J = 1.9H), 6.77 (t, 1H, J = 1.9H), 6.70 (t, 1H, J = 2.1H), 3.79 (s, 3H), 2.72 (s, 3H) 1.84 (s, 6H) 56 N-(3-chloro-5-(4- LC/MS ESI (+): 576 (M + 1) chlorophenoxy)phenyl)-5-(4- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.73 (s, 1H), (methylsulfonyl)tetrahydro-2H-pyran-4- 8.32 (s, 1H), 8.27 (s, 1H), 8.16 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.76 (s, 1H), 7.73 (d, 1H, J = 9.1 Hz), 7.51 (d, 2H, J = 8.8 Hz), 7.36 (s, 1H), 7.18 (d, 2H, J = 8.8 Hz), 6.93 (s, 1H), 3.91 (d, 2H, J = 9.7 Hz), 3.20 (t, 2H, J = 11.7 Hz), 2.74 (d, 2H, J = 13.3 Hz), 2.65 (s, 3H), 2.33 (t, 2H, J = 12.3 Hz) 57 N-(3-chloro-5-(4- LC/MS ESI (+): 578 (M + 1) chlorophenoxy)phenyl)-5-(2-((2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.72 (s, 1H), methoxyethyl)sulfonyl)propan-2- 8.33 (s, 1H), 8.22 (s, 1H), 8.11 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.6 Hz), 7.74-7.77 (m, 2H), 7.52 (d, 2H, J = 8.9 Hz), 7.37 (s, 1H), 7.19 (d, 2H, J = 8.9 Hz), 6.93 (s, 1H), 3.49 (t, 2H, J = 6.3 Hz), 3.11-3.14 (m, 5H), 1.85 (s, 6H) 58 N-(3-chloro-5-(4- LC/MS ESI (+): 534 (M + 1) chlorophenoxy)phenyl)-6-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.69 (s, 1H), (methylsulfonyl)propan-2- 8.30-8.33 (s, 2H), 8.02 (d, 1H, J = 8.6 Hz), yl)benzo[b]thiophene-2-carboxamide 7.76 (s, 1H), 7.74 (d, 1H, J = 8.6 Hz), 7.51 (d, 2H, J = 8.9 Hz), 7.37 (s, 1H), 7.18 (d, 2H, J = 8.9 Hz), 6.92 (s, 1H), 2.73 (s, 3H), 1.84 (s, 6H) 59 N-(3-(azetidin-1-yl)-5-(4- LC/MS ESI (+): 555 (M + 1) chlorophenoxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.41 (s, 1H), (methylsulfonyl)propan-2- 8.34 (s, 1H), 8.18 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.74 (d, 1H, J = 8.8 Hz), 7.45 (d, 2H, J = 8.8 Hz), 7.08 (d, 2H, J = 9.2 Hz), 6.76-6.78 (m, 2H), 5.89 (s, 1H), 3.82 (t, 4H, J = 6.4 Hz), 2.74 (s, 3H), 2.33-2.34 (m, 2H), 1.85 (s, 6H) 60 N-(3-chloro-5-((6-chloropyridin-3- LC/MS ESI (+): 535 (M + 1) yl)oxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.73 (s, 1H), (methylsulfonyl)propan-2- 8.33-8.37 (m, 2H), 8.22 (s, 1H), 8.10 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.6 Hz), 7.71-7.79 (m, 3H), 7.62 (d, 1H, J = 8.7 Hz), 7.39 (s, 1H), 7.03 (s, 1H), 2.73 (s, 3H), 1.85 (s, 6H) 61 N-(3-chloro-5-((5-chloropyridin-2- LC/MS ESI (+): 535 (M + 1) yl)oxy)phenyl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.76 (s, 1H), (methylsulfonyl)propan-2- 8.36 (s, 1H), 8.28 (d, 1H, J = 2.6 Hz), 8.22 (s, yl)benzo[b]thiophene-2-carboxamide 1H), 8.10 (d, 1H, J = 8.7 Hz), 7.03 (dd, 1H, J = 8.7, 2.7 Hz), 7.74-7.80 (m, 2H), 7.55 (s, 1H), 7.21 (d, 1H, J = 8.7 Hz), 7.09 (s, 1H), 2.73 (s, 3H), 1.85 (s, 6H)

Example 62) Synthesis of N-(2-chloro-6-(3,5-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 2-chloro-6-(3,5-dichlorophenoxy)pyridine-4-amine

[0519] 2,6-Dichloropyridine-4-amine (200.0 mg, 1.22 mmol) and 3,5-dichlorophenol (400.0 mg, 2.45 mmol) were dissolved in sulfolane (6.1 mL) and K.sub.2CO.sub.3 (339.0 mg, 2.45 mmol) was added. The reaction mixture was stirred at 160° C. for 16 hours, cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with 1N NaOH aqueous solution and brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain 2-chloro-6-(3,5-dichlorophenoxy)pyridine-4-amine (121.0 mg, 34%) as a white solid.

[0520] LC/MS ESI (+): 289 (M+1)

[0521] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 7.46 (s, 1H), 7.24 (d, 2H, J=1.8 Hz), 6.63 (brs, 2H), 6.35 (d, 1H, J=1.6 Hz), 6.00 (d, 1H, J=1.6 Hz)

(b) Synthesis of N-(2-chloro-6-(3,5-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0522] 5-(2-(Methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (50.0 mg, 0.16 mmol) was dissolved in CH.sub.2Cl.sub.2 (1.6 mL), and DMF (1.2 μL, 0.01 mmol) and (COCl).sub.2 (16.1 μL, 0.18 mmol) were added. The reaction mixture was stirred at 25° C. for 2 hours and concentrated under reduced pressure to obtain 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carbonyl chloride. To the residue, 2-chloro-6-(3,5-dichlorophenoxy)pyridine-4-amine (50.9 mg, 0.17 mmol) and pyridine (550.0 μL) were added, stirred at 30° C. for 16 hours, and concentrated under reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain N-(2-chloro-6-(3,5-dichlorophenoxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (62.0 mg, 65%) as a white solid.

[0523] LC/MS ESI (+): 569 (M+1)

[0524] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.14 (brs, 1H), 8.42 (s, 1H), 8.26 (d, 1H, J=2.8 Hz), 8.13 (d, 1H, J=8.7 Hz), 7.77 (dd, 1H, J=8.7, 1.8 Hz), 7.71 (d, 1H, J=1.3 Hz), 7.56 (t, 1H, J=1.8 Hz), 7.44 (d, 2H, J=1.8 Hz), 7.39 (d, 1H, J=1.4 Hz), 2.74 (s, 3H), 1.86 (s, 6H)

[0525] Compounds from Example 63 to Example 86 were synthesized through the synthesis route of Example 62, and data of these compounds are listed as follows.

TABLE-US-00005 TABLE 5 Ex. Compound Analysis data 63 N-(6-chloro-4-(4- LC/MS ESI (+): 535 (M + 1) chlorophenoxy)pyridin-2-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.59 (s, 1H), (methylsulfonyl)propan-2- 8.60 (s, 1H), 8.13 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.74-7.77 (m, 2H), 7.59 (d, 2H, J = 8.8 Hz), 7.33 (d, 2H, J = 8.8 Hz), 6.94 (s, 1H), 2.75 (s, 3H), 1.86 (s, 6H) 64 N-(2-chloro-6-(4- LC/MS ESI (+): 535 (M + 1) chlorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.10 (s, 1H), (methylsulfonyl)propan-2- 8.39 (s, 1H), 8.26 (s, 1H), 8.12 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.79 (d, 1H, J = 8.8 Hz), 7.67 (s, 1H), 7.53 (d, 2H, J = 8.8 Hz), 7.33 (s, 1H), 7.27 (d, 2H, J = 8.8 Hz), 2.75 (s, 3H), 1.86 (s, 6H) 65 N-(2-chloro-6-((6-chloropyridin-3- LC/MS ESI (+): 536 (M + 1) yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.18 (brs, (methylsulfonyl)propan-2- 1H), 8.39-8.41 (m, 2H), 8.25 (s, 1H), 8.11 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.83 (d, 1H, J = 8.6 Hz), 7.76 (d, 1H, J = 8.7 Hz), 7.63-7.67 (m, 2H), 7.44 (s, 1H), 2.74 (s, 3H), 1.86 (s, 6H) 66 N-(4-chloro-6-(4- LC/MS ESI (+): 535 (M + 1) chlorophenoxy)pyridin-2-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.27 (s, 1H), (methylsulfonyl)propan-2- 8.54 (s, 1H), 8.15 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 8.04 (s, 1H), 7.75 (dd, 1H, J = 8.8, 1.6 Hz), 7.51 (d, 2H, J = 8.8 Hz), 7.28 (d, 2H, J = 8.8 Hz), 6.93 (s, 1H), 2.74 (s, 3H), 1.85 (s, 6H) 67 N-(2-chloro-6-(4- LC/MS ESI (+): 569 (M + 1) (trifluoromethyl)phenoxy)pyridin-4-yl)- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.15 (s, 1H), 5-(2-(methylsulfonyl)propan-2- 8.42 (s, 1H), 8.27 (s, 1H), 8.14 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.86 (d, 2H, J = 8.8 Hz), 7.79 (dd, 1H, J = 8.4, 2.0 Hz), 7.73 (s, 1H), 7.43-7.46 (m, 3H), 2.75 (s, 3H), 1.87 (s, 6H) 68 N-(2-chloro-6-(4- LC/MS ESI (+): 519 (M + 1) fluorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.11 (s, 1H), (methylsulfonyl)propan-2- 8.41 (s, 1H), 8.27 (d, 1H, J = 1.6 Hz), 8.14 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.8 Hz), 7.79 (dd, 1H, J = 8.7, 1.9 Hz), 7.68 (d, 1H, J = 1.2 Hz), 7.27-7.35 (m, 5H), 2.76 (s, 3H) 1.87 (s, 6H) 69 N-(2-bromo-6-(4- LC/MS ESI (−): 577 (M − 1) chlorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.06 (s, 1H), (methylsulfonyl)propan-2- 8.41 (s, 1H), 8.26 (s, 1H), 8.13 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.83 (d, 1H, J = 1.6 Hz), 7.77 (dd, 1H, J = 8.8, 2.0 Hz), 7.54 (d, 2H, J = 8.8 Hz), 7.37 (s, 1H), 7.27 (d, 2H, J = 8.8 Hz), 2.75 (s, 3H), 1.87 (s, 6H) 70 N-(2-chloro-6-(3-chloro-5- LC/MS ESI (+): 565 (M + 1) methoxyphenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.15 (brs, (methylsulfonyl)propan-2- 1H), 8.40 (s, 1H), 8.23 (d, 1H, J = 1.6 Hz), yl)benzo[b]thiophene-2-carboxamide 8.10 (d, 1H, J = 8.7 Hz), 7.75 (dd, 1H, J = 8.7, 1.9 Hz), 7.69 (d, 1H, J = 1.4 Hz), 7.30 (d, 1H, J = 1.4 Hz), 6.96 (s, 1H), 6.91 (s, 1H), 6.81 (s, 1H), 3.79 (s, 3H), 2.70 (s, 3H), 1.85 (s, 6H) 71 N-(2-chloro-6-(3-chloro-4- LC/MS ESI (+): 553 (M + 1) fluorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.08 (brs, (methylsulfonyl)propan-2- 1H), 8.39 (s, 1H), 8.24 (d, 1H, J = 1.6 Hz), yl)benzo[b]thiophene-2-carboxamide 8.10 (d, 1H, J = 8.7 Hz), 7.76 (dd, 1H, J = 8.7, 1.9 Hz), 7.66 (s, 1H), 7.58 (dd, 1H, J = 6.3, 2.9 Hz), 7.52 (t, 1H, J = 9.0 Hz), 7.33 (d, 1H, J = 1.4 Hz), 7.27 (m, 1H), 2.70 (s, 3H), 1.85 (s, 6H) 72 N-(2-chloro-6-(4-chloro-3- LC/MS ESI (+): 553 (M + 1) fluorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.18 (brs, (methylsulfonyl)propan-2- 1H), 8.40 (s, 1H), 8.25 (s, 1H), 8.12 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.77 (dd, 1H, J = 8.7, 1.8 Hz), 7.66-7.71 (m, 2H), 7.46 (dd, 1H, J = 10.2, 2.7 Hz), 7.37 (s, 1H), 7.15 (m, 1H), 2.74 (s, 3H), 1.85 (s, 6H) 73 N-(2-chloro-6-(4- C/MS ESI (+): 533 (M + 1) chlorophenoxy)pyridin-4-yl)-5-(1,1- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.07 (s, 1H), dioxidotetrahydrothiophen-2- 8.38 (s, 1H), 8.11 (d, 1H, J = 8.5 Hz), 8.05 (s, yl)benzo[b]thiophene-2-carboxamide 1H), 7.67 (s, 1H), 7.52-7.55 (m, 3H), 7.33 (s, 1H), 7.26 (d, 2H, J = 8.9 Hz), 4.55 (m, 1H), 3.20-3.26 (m, 2H), 2.38-2.44 (m, 2H), 2.12-2.28 (m, 2H) 74 N-(2-chloro-6-(4- LC/MS ESI (+): 547 (M + 1) chlorophenoxy)pyridin-4-yl)-5-(1,1- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.07 (s, 1H), dioxidotetrahydro-2H-thiopyran-2- 8.39 (s, 1H), 8.09 (d, 1H, J = 8.5 Hz), 8.03 (s, yl)benzo[b]thiophene-2-carboxamide 1H), 7.67 (s, 1H), 7.51-7.54 (m, 3H), 7.33 (s, 1H), 7.26 (d, 2H, J = 8.9 Hz), 4.60 (m, 1H), 3.25-3.33 (m, 2H), 1.67-2.41 (m, 6H) 75 N-(2-chloro-6-(4- LC/MS ESI (+): 536 (M + 1) chlorophenoxy)pyrimidin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 12.11 (brs, (methylsulfonyl)propan-2- 1H), 8.59 (s, 1H), 8.15 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.76 (d, 1H, J = 8.7 Hz), 7.66 (s, 1H), 7.56 (d, 2H, J = 8.8 Hz), 7.34 (d, 2H, J = 8.8 Hz), 2.75 (s, 3H), 1.85 (s, 6H) 76 N-(6-chloro-2-(4- LC/MS ESI (+): 536 (M + 1) chlorophenoxy)pyrimidin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 12.00 (brs, (methylsulfonyl)propan-2- 1H), 8.56 (s, 1H), 8.17 (s, 1H), 8.09 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.7 Hz), 7.98 (s, 1H), 7.75 (d, 1H, J = 10.2 Hz), 7.52 (d, 2H, J = 8.8 Hz), 7.33 (d, 2H, J = 8.8 Hz), 2.74 (s, 3H), 1.85 (s, 6H) 77 N-(2-(4-chlorophenoxy)-6- LC/MS ESI (+): 519 (M + 1) fluoropyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d6): δ 11.17 (s, 1H), (methylsulfonyl)propan-2- 8.41 (s, 1H), 8.26 (s, 1H), 8.13 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.4 Hz), 7.78 (d, 1H, J = 8.4 Hz), 7.54 (d, 2H, J = 8.8 Hz), 7.32 (s, 1H), 7.28 (d, 2H, J = 8.8 Hz), 7.21 (s, 1H), 2.75 (s, 3H), 1.86 (s, 6H) 78 N-(2-(bicyclo[2.2.1]hept-5-en-2-yloxy)- LC/MS ESI (+): 517 (M + 1) 6-chloropyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d6): δ 10.89 (s, 1H), (methylsulfonyl)propan-2- 8.37 (s, 1H), 8.24 (s, 1H), 8.11 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.77 (d, 1H, J = 8.7 Hz), 7.41 (s, 1H), 7.14 (s, 1H), 6.38 (m, 1H), 6.01 (m, 1H), 5.40 (m, 1H), 3.25 (s, 1H), 2.86 (s, 1H), 2.73 (s, 3H), 2.22 (m, 1H), 1.85 (s, 6H), 1.42 (m, 2H), 0.92 (d, 1H, J = 13.0 Hz) 79 N-(2-chloro-6-(3,4- LC/MS ESI (+): 537 (M + 1) difluorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.11 (s, 1H), (methylsulfonyl)propan-2- 8.41 (s, 1H), 8.26 (s, 1H), 8.15 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 8.8 Hz), 7.80 (d, 1H, J = 8.8 Hz), 7.69 (s, 1H), 7.55-7.57 (m, 2H), 7.36 (s, 1H), 7.14-7.15 (m, 1H), 2.75 (s, 3H) 1.86 (s, 6H) 80 N-(2-chloro-6-(3- LC/MS ESI (+): 535 (M + 1) chlorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ (methylsulfonyl)propan-2- 11.08 (brs, 1H), 8.31 (s, 1H), 8.17 (s, 1H), yl)benzo[b]thiophene-2-carboxamide 8.04 (d, 1H, J = 8.8 Hz), 7.69 (d, 1H, J = 8.8 Hz), 7.61 (s, 1H), 7.43 (t, 1H, J = 8.0 Hz), 7.26-7.31 (m, 3H), 7.13 (d, 1H, J = 8.6 Hz), 2.67 (s, 3H), 1.89 (s, 6H) 81 N-(2-chloro-6-(3- LC/MS ESI (+): 585 (M + 1) (trifluoromethoxy)phenoxy)pyridin-4- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ yl)-5-(2-(methylsulfonyl)propan-2- 11.05 (s, 1H), 8.33 (s, 1H), 8.19 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 1.6 Hz), 8.05 (d, 1H, J = 8.7 Hz), 7.70 (dd, 1H, J = 8.7, 1.6 Hz), 7.62 (d, 1H, J = 1.2 Hz), 7.53 (t, 1H, J = 7.2 Hz), 7.32 (s, 1H), 7.21-7.26 (m, 3H), 2.67 (s, 3H), 1.79 (s, 6H) 82 N-(2-chloro-6-(3,4- LC/MS ESI (+): 569 (M + 1) dichlorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ (methylsulfonyl)propan-2- 11.04 (s, 1H), 8.34 (s, 1H), 8.19 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 1.6 Hz), 8.06 (d, 1H, J = 8.7 Hz), 7.71 (dd, 1H, J = 8.7, 1.6 Hz), 7.67 (d, 1H, J = 8.8 Hz), 7.53 (d, 1H, J = 1.6 Hz), 7.32 (d, 1H, J = 2.4 Hz), 7.3 (d, 1H, J = 2.4 Hz), 7.21 (dd, 1H, J = 8.0, 2.4 Hz), 2.67 (s, 3H), 1.79 (s, 6H) 83 N-(2-chloro-6-(4-chloro-2- LC/MS ESI (+): 553 (M + 1) fluorophenoxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ (methylsulfonyl)propan-2- 11.04 (s, 1H), 8.33 (s, 1H), 8.18 (s, 1H), yl)benzo[b]thiophene-2-carboxamide 8.06 (d, 1H, J = 8.7 Hz), 7.71 (dd, 1H, J = 8.7, 1.6 Hz), 7.61 (s, 1H), 7.41 (d, 2H, J = 8.8 Hz), 7.29 (d, 2H, J = 8.8 Hz), 2.67 (s, 3H), 1.78 (s, 6H) 84 N-(2-chloro-6-(4- LC/MS ESI (+): 585 (M + 1) (trifluoromethoxy)phenoxy)pyridin-4- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ yl)-5-(2-(methylsulfonyl)propan-2- 11.11 (s, 1H), 8.40 (s, 1H), 8.26 (s, 1H), 8.13 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.8 Hz), 7.77 (d, 1H, J = 8.8 Hz), 7.68 (s, 1H,) 7.50 (s, 1H), 7.48 (s, 1H), 7.35-7.37 (m, 3H), 2.74 (s, 3H), 1.85 (s, 6H) 85 N-(2-chloro-6-((5-chloropyridin-2- LC/MS ESI (+): 536 (M + 1) yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ (methylsulfonyl)propan-2- 11.09 (s, 1H), 8.34 (s, 1H), 8.31 (d, 1H, yl)benzo[b]thiophene-2-carboxamide J = 2.4 Hz), 8.19 (s, 1H), 8.01-8.07 (m, 2H), 7.71 (d, 1H, J = 8.8 Hz), 7.68 (d, 1H, J = 1.2 Hz), 7.41 (s, 1H), 7.23 (d, 1H, J = 8.8 Hz), 2.62 (s, 3H), 1.79 (s, 6H) 86 N-(2-chloro-6-((4- LC/MS ESI (+): 549 (M + 1) chlorobenzyl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ (methylsulfonyl)propan-2- 10.91 (s, 1H), 8.32 (s, 1H), 8.18 (s, 1H), yl)benzo[b]thiophene-2-carboxamide 8.05 (d, 1H, J = 8.8 Hz), 7.70 (d, 1H, J = 8.8 Hz), 7.38-7.44 (m, 5H) 7.24 (s, 1H), 5.26 (s, 2H), 2.67 (s, 3H), 1.78 (s, 6H)

Example 87) Synthesis of N-(3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 3-(2-(3-chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenyl trifluoromethanesulfonate

[0526] 3-(2-(3-Chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenol (100.0 mg, 0.27 mmol) was dissolved in CH.sub.2Cl.sub.2 (2.7 mL), and pyridine (109.0 pt, 1.35 mmol) and Tf.sub.2O (45.0 μL, 0.27 mmol) were slowly added dropwise at 0° C. The reaction mixture was stirred at 0° C. for 2 hours, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 3-(2-(3-chloro-5-nitrophenyl)propan-2-yl)-5-(trifluoromethoxy)phenyl trifluoromethanesulfonate (120.0 mg, 88%) as a colorless liquid.

[0527] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.13 (t, 1H, J=1.9 Hz), 7.99 (t, 1H, J=1.9 Hz), 7.45 (t, 1H, J=1.8 Hz), 7.08-7.10 (m, 2H), 7.04 (t, 1H, J=1.9 Hz), 1.75 (s, 6H)

(b) Synthesis of 1-chloro-3-nitro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)benzene

[0528] 3-(2-(3-Chloro-5-nitrophenyl)propan-2-yl)-5-(tri fluoromethoxy)phenyl trifluoromethanesulfonate (280.0 mg, 0.55 mmol) was dissolved in anhydrous DMF (5.5 mL), and 1-(trimethylsilyl)-1-propyne (123.0 μL, 0.83 mmol), Pd(PPh.sub.3).sub.4 (64.0 mg, 0.06 mmol), CuI (21.0 mg, 0.11 mmol) and DIPEA (480.0 μL, 2.75 mmol) were added at room temperature. The reaction mixture was stirred at 90° C. for 15 hours, cooled to room temperature, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:CH.sub.2Cl.sub.2=4:1) to obtain 1-chloro-3-nitro-5-(2-(3-(prop-1-yn-1-yl)-5-(tri fluoromethoxy)phenyl)propan-2-yl)benzene (120.0 mg, 55%) as a colorless liquid.

[0529] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.08 (t, 1H, J=1.9 Hz), 7.99 (t, 1H, J=1.9 Hz), 7.46 (t, 1H, J=1.8 Hz), 7.11-7.13 (m, 2H), 6.94 (s, 1H), 2.04 (s, 3H), 1.70 (s, 6H)

[0530] The synthesis procedure of Example 1-g was repeated except for using 1-chloro-3-nitro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)benzene (120.0 mg, 0.32 mmol) as a starting material to obtain 3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)aniline (93.0 mg, 84%).

[0531] LC/MS ESI (+): 368 (M+1)

(d) Synthesis of N-(3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0532] The synthesis procedure of Example 1-h was repeated except for using 3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)aniline (55.0 mg, 0.15 mmol) as a starting material to obtain N-(3-chloro-5-(2-(3-(prop-1-yn-1-yl)-5-(trifluoromethoxy)phenyl)propan-2-yl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (23.5 mg, 33%).

[0533] LC/MS ESI (+): 648 (M+1)

[0534] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.65 (s, 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.10 (d, 1H, J=8.8 Hz), 7.90 (s, 1H), 7.74 (d, 1H, J=8.8 Hz), 7.50 (s, 1H), 7.19-7.22 (m, 3H), 7.07 (s, 1H), 2.73 (s, 3H), 2.03 (s, 3H), 1.85 (s, 6H), 1.65 (s, 6H)

Example 88) Synthesis of N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 4-(4-chlorophenyl)-4-methyl-3-oxopentanenitrile

[0535] 2-(4-Chlorophenyl)-2-methylpropanic acid (500.0 mg, 2.52 mmol) was dissolved in THF (10.0 mL), carbonyldiimidazole (490.0 mg, 3.02 mmol) was added, and stirred for 2 hours. To the reaction mixture was added a solution prepared by dissolving CH.sub.3CN (0.2 mL, 8.31 mmol) in THF (10.0 mL), adding 1.6M solution of n-BuLi in THF (4.7 mL, 7.56 mmol) slowly dropwise at −78° C. and stirring for 1 hour. The resulting mixure was stirred at −78° C. for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:CH.sub.2Cl.sub.2=1:2) to obtain 4-(4-chlorophenyl)-4-methyl-3-oxopentanenitrile (333.0 mg, 59%) as an off-white oil.

[0536] LC/MS ESI (−): 220 (M−1)

[0537] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.38 (d, 2H, J=8.4 Hz), 7.19 (d, 2H, J=8.8 Hz), 3.30 (s, 2H), 1.53 (s, 6H)

(b) Synthesis of 1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazole-5-amine

[0538] tert-Butylhydrazine chloride (463.0 mg, 3.72 mmol) was dissolved in EtOH (1.9 mL), and NaOH (119.0 g, 2.97 mmol) was added. 4-(4-Chlorophenyl)-4-methyl-3-oxopentanenitrile (330.0 mg, 1.49 mmol) in EtOH (1.0 mL) was added to the reaction mixture dropwise. The reaction mixture was stirred at 80° C. for 12 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was dried over Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:1) to obtain 1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazole-5-amine (130.0 mg, 30%) as a whilte solid.

[0539] LC/MS ESI (+): 292 (M+1)

[0540] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.25 (d, 2H, J=9.2 Hz), 7.19 (d, 2H, J=8.8 Hz), 5.24 (s, 1H), 3.41 (s, 2H), 1.62 (s, 9H), 1.59 (s, 6H)

(c) Synthesis of N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0541] The synthesis procedure of Example 1-h was repeated except for using 1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazole-5-amine (100.0 mg, 0.34 mmol) as a starting material to obtain N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (78.0 mg, 40%).

[0542] LC/MS ESI (+): 572 (M+1)

[0543] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.35 (s, 1H), 8.27 (s, 1H), 8.26 (s, 1H), 8.10 (d, 1H, J=8.8 Hz), 7.76 (d, 1H, J=8.8 Hz), 7.30-7.35 (m, 4H), 6.08 (s, 1H), 2.74 (s, 3H), 1.85 (s, 6H), 1.63 (s, 6H), 1.57 (s, 9H).

Example 89) Synthesis of N-(3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0544] N-(1-(tert-butyl)-3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (30.0 mg, 0.05 mmol) was dissolved in formic acid (4.0 mL). The reaction mixture was stirred at 80° C. for 12 hours and concentrated under reduced pressure, basified with sat. NaHCO.sub.3 aqueous solution (pH=9) and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain N-(3-(2-(4-chlorophenyl)propan-2-yl)-1H-pyrazol-5-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (17.0 mg, 67%) as a white solid.

[0545] LC/MS ESI (+): 516 (M+1)

[0546] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 12.30 (s, 1H), 11.23 (s, 1H), 8.44 (s, 1H), 8.13 (s, 1H), 8.09 (d, 1H, J=8.8 Hz), 7.74 (d, 1H, J=8.8 Hz), 7.38 (d, 2H, J=8.4 Hz), 7.29 (d, 2H, J=8.4 Hz), 6.50 (s, 1H), 2.74 (s, 3H), 1.86 (s, 6H), 1.67 (s, 6H)

Example 90 and Example 91) Synthesis of N-(2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide and N-(4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 4,6-dichloro-N-methoxy-N-methylisonicotinamide

[0547] 4,6-Dichloroisonicotinic acid (3.0 g, 15.6 mmol) was dissolved in anhydrous CH.sub.2Cl.sub.2 (100.0 mL), and (COC).sub.2 (2.1 mL, 23.40 mmol) and anhydrous DMF were added dropwise in a catalytic amount, followed by stirring at 0° C. for 1 hour. The reaction mixture was dried under reduced pressure for 1 hour, the residue was dissolved in anhydrous CH.sub.2Cl.sub.2 (100.0 mL), and N,O-dimethylhydroxyamine (4.6 g, 46.80 mmol) and pyridine (7.5 mL, 93.60 mmol) were added at 0° C. The reaction mixture was stirred at 0° C. for 1 hour, H.sub.2O was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=1:4) to obtain 4,6-dichloro-N-methoxy-N-methylisonicotinamide (3.5 g, 83%) as a white solid.

[0548] LC/MS ESI (+): 235 (M+1)

[0549] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.56 (brs, 1H), 7.44 (s, 1H), 3.80 (s, 3H), 3.36 (s, 3H)

(b) Synthesis of (4,6-di chloropyridin-2-yl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone

[0550] 1-Bromo-3-methoxy-5-(trifluoromethoxy)benzene (5.0 g, 18.45 mmol) was dissolved in THF (90.0 mL), 1.7M solution of tert-BuLi in pentane (11.4 mL, 19.30 mmol) was added dropwise at −78° C., and stirred for 1 hour. 4,6-Dichloro-N-methoxy-N-methylisonicotinamide (3.5 g, 14.88 mmol) in THF (10.0 mL) was slowly added, and the reaction mixture was stirred at 0° C. for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:CH.sub.2Cl.sub.2=1:10) to obtain (4,6-dichloropyridin-2-yl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone (2.4 g, 44%) as a yellow solid.

[0551] LC/MS ESI (+): 366 (M+1)

[0552] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.00 (s, 1H), 7.63 (s, 1H), 7.61 (s, 1H), 7.59 (s, 1H), 7.01 (s, 1H), 3.89 (s, 3H)

[0553] The synthesis procedure of Example 1-c was repeated except for using (4,6-dichloropyridin-2-yl)(3-methoxy-5-(trifluoromethoxy)phenyl)methanone (2.4 g, 6.55 mmol) as a starting material to obtain 2,4-dichloro-6-(dichloro(3-methoxy-5-(trifluoromethoxy)phenyl)methyl)pyridine (2.1 g, 76%).

[0554] LC/MS ESI (+): 420 (M+1)

[0555] .sup.1H-NMR (400 MHz, CDCl.sub.3): 7.76 (s, 1H), 7.37 (s, 1H), 7.13 (s, 1H), 7.06 (s, 1H), 6.77 (s, 1H), 3.84 (s, 3H)

(d) Synthesis of 2,4-di chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine

[0556] The synthesis procedure of Example 1-d was repeated except for using 2,4-dichloro-6-(dichloro(3-methoxy-5-(trifluoromethoxy)phenyl)methyl)pyridine (2.1 g, 4.98 mmol) as a starting material to obtain 2,4-dichloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine (1.3 g, 69%) as an off-white oil.

[0557] LC/MS ESI (+): 380 (M+1)

[0558] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.19 (s, 1H), 6.94 (s, 1H), 6.73 (s, 1H), 6.70 (s, 1H), 6.62 (s, 1H), 3.79 (s, 3H), 1.69 (s, 6H)

(e) Synthesis of 2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine-4-amine and (f) synthesis of 4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine-2-amine

[0559] 2,4-Dichloro-6-(2-(3-methoxy-5-(tri fluoromethoxy)phenyl)propan-2-yl)pyridine (50.0 mg, 0.13 mmol), NaN.sub.3 (17.0 mg, 0.26 mmol), Cu.sub.2O (18.7 mg, 0.131 mmol) and L-proline (19.5 mg, 0.17 mmol) were dissolved in anhydrous DMSO (1.0 mL). The reaction mixture was stirred at 100° C. for 12 hours, cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=9:1) to obtain 2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine-4-amine (14.0 mg, 30%) and 4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyri dine-2-amine (4.0 mg, 8%) as an off-white oil.

[0560] (e) LC/MS ESI (+): 361 (M+1)

[0561] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 6.74 (s, 1H), 6.72 (s, 1H), 6.96 (s, 1H), 6.37 (d, 1H, J=1.2 Hz), 6.14 (d, 1H, J=1.2 Hz), 4.13 (brs, 2H), 3.76 (s, 3H), 1.64 (s, 6H)

[0562] (f) LC/MS ESI (+): 361 (M+1)

[0563] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 6.72 (s, 1H), 6.71 (s, 1H), 6.59 (s, 1H), 6.48 (s, 1H), 6.32 (s, 1H), 4.43 (brs, 2H), 3.77 (s, 3H), 1.62 (s, 6H)

(g) Synthesis of N-(2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0564] The synthesis procedure of Example 1-h was repeated except for using 2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine-4-amine (38.0 mg, 0.11 mmol) as a starting material to obtain N-(2-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (20.0 mg, 30%) as a white solid.

[0565] LC/MS ESI (+): 641 (M+1)

[0566] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.99 (s, 1H), 8.39 (s, 1H), 8.24 (s, 1H), 8.13 (d, 1H, J=8.8 Hz), 7.89 (s, 1H), 7.77 (d, 1H, J=8.8 Hz), 7.56 (s, 1H), 6.84 (s, 1H), 6.83 (s, 1H), 6.77 (s, 1H), 3.79 (s, 3H), 2.75 (s, 3H), 1.86 (s, 6H), 1.68 (s, 6H)

(h) Synthesis of N-(4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0567] The synthesis procedure of Example 1-h was repeated except for using 4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridine-2-amine (20.0 mg, 0.06 mmol) as a starting material to obtain N-(4-chloro-6-(2-(3-methoxy-5-(trifluoromethoxy)phenyl)propan-2-yl)pyridin-2-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (12.0 mg, 34%) as a white solid.

[0568] LC/MS ESI (+): 641 (M+1)

[0569] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.16 (s, 1H), 8.64 (s, 1H), 8.19 (s, 1H), 8.11 (d, 1H, J=8.8 Hz), 8.09 (d, 1H, J=2.0 Hz), 7.77 (dd, 1H, J=8.8, 2.0 Hz), 7.20 (s, 1H), 6.86 (s, 1H), 6.79-6.81 (m, 2H), 3.78 (s, 3H), 2.76 (s, 3H), 1.86 (s, 6H), 1.74 (s, 6H)

Example 92) Synthesis of N-(3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 4-(3-bromo-5-chlorophenoxy)-2,2,6,6-tetramethylpiperidine

[0570] 1-Bromo-3-chloro-5-nitrobenzene (200.0 mg, 0.42 mmol) was dissolved in anhydrous DMF (2.1 mL), and 2,2,6,6-tetramethylpiperidin-4-ol (66.0 mg, 0.42 mmol) and 60 wt % NaH (50.4 mg, 1.26 mmol) were added. The reaction mixture was stirred at room temperature for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 4-(3-bromo-5-chlorophenoxy)-2,2,6,6-tetramethylpiperidine (160.0 mg, 54%) as an off-white oil.

[0571] LC/MS ESI (+): 346 (M+1)

[0572] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.09 (s, 1H), 6.93 (s, 1H), 6.81 (s, 1H), 4.60 (m, 1H), 2.02-2.06 (m, 2H), 1.20-1.30 (m, 14H)

(b) Synthesis of 3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)aniline

[0573] The synthesis procedure of Example 91-e was repeated except for using 4-(3-bromo-5-chlorophenoxy)-2,2,6,6-tetramethylpiperidine (34.0 mg, 0.10 mmol) as a starting material to obtain 3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)aniline (16.0 mg, 58%).

[0574] LC/MS ESI (+): 283 (M+1)

[0575] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 6.31 (s, 1H), 6.29 (s, 1H), 6.10 (s, 1H), 4.58 (m, 1H), 3.70 (brs, 2H), 2.03-2.05 (m, 2H), 1.18-1.23 (m, 14H)

(c) Synthesis of N-(3-chloro-5-(2,2,6,6-tetramethylpiperidin-4-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0576] The synthesis procedure of Example 1-h was repeated except for using 3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)aniline (16.0 mg, 0.06 mmol) as a starting material to obtain N-(3-chloro-5-((2,2,6,6-tetramethylpiperidin-4-yl)oxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (9.0 mg, 28%) as a white solid.

[0577] LC/MS ESI (+): 563 (M+1)

[0578] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.53 (s, 1H), 8.28 (s, 1H), 8.16 (s, 1H), 8.03 (d, 1H, J=8.8 Hz), 7.68 (dd, 1H, J=8.8, 2.0 Hz), 7.41 (s, 1H), 7.33 (s, 1H), 6.73 (s, 1H), 4.66-4.71 (m, 1H), 1.88 (dd, 2H, J=12.4, 4.0 Hz), 1.79 (s, 6H), 1.14 (s, 6H), 1.07-1.10 (m, 2H), 1.02 (s, 6H)

Example 93) Synthesis tert-butyl (2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate

(a) Synthesis of 1-(4-chlorophenoxy)-3-methoxy-5-nitrobenzene

[0579] The synthesis procedure of Example 40-a was repeated except for using 1-bromo-3-methoxy-5-nitrobenzene (500.0 mg 1.71 mmol) as a starting material to obtain 1-(4-chlorophenoxy)-3-methoxy-5-nitrobenzene (400.0 mg, 66%).

[0580] LC/MS ESI (+): 280 (M+1)

[0581] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.48 (t, 1H, J=2.2 Hz), 7.37 (t, 1H, J=2.1 Hz), 7.36 (d, 2H, J=8.8 Hz), 7.00 (d, 2H, J=8.9 Hz), 6.83 (t, 1H, J=2.1 Hz), 3.87 (s, 3H)

(b) Synthesis of 3-(4-chlorophenoxy)-5-nitrophenol

[0582] The synthesis procedure of Example 1-e was repeated except for using 1-(4-chlorophenoxy)-3-methoxy-5-nitrobenzene (396.0 mg, 1.42 mmol) as a starting material to obtain 3-(4-chlorophenoxy)-5-nitrophenol (307.0 mg, 82%).

[0583] LC/MS ESI (+): 266 (M+1)

[0584] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.39 (t, 1H, J=2.2 Hz), 7.35 (d, 2H, J=8.9 Hz), 7.33 (t, 1H, J=2.1 Hz), 6.98 (d, 2H, J=8.9 Hz), 6.74 (t, 1H, J=2.2 Hz)

[0585] 3-(4-Chlorophenoxy)-5-nitrophenol (297.0 mg, 1.11 mmol) was dissolved in anhydrous DMF (10.0 mL), K.sub.2CO.sub.3 (231.0 mg, 1.68 mmol) was added, stirred at room temperature for 10 minutes, and tert-butyl (2-bromoethyl)carbamate (300.0 mg, 1.34 mmol) was added. The reaction mixture was stirred at room temperature for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=6:1) to obtain tert-butyl (2-(3-(4-chlorophenoxy)-5-nitrophenoxy)ethyl)carbamate (435.0 mg, 95%).

[0586] LC/MS ESI (+): 409 (M+1)

[0587] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.44 (t, 1H, J=2.1 Hz), 7.37 (t, 1H, J=2.1 Hz), 7.36 (d, 2H, J=8.9 Hz), 6.98 (d, 2H, J=8.9 Hz), 6.79 (t, 1H, J=2.2 Hz), 4.90 (brs, 1H), 4.04 (t, 2H, J=5.1 Hz), 3.51-3.55 (m, 2H), 1.43 (s, 9H)

(d) Synthesis of tert-butyl (2-(3-amino-5-(4-chlorophenoxy)phenoxy)ethyl)carbamate

[0588] The synthesis procedure of Example 1-g was repeated except for using tert-butyl (2-(3-(4-chlorophenoxy)-5-nitrophenoxy)ethyl)carbamate (425.0 mg, 1.04 mmol) as a starting material to obtain tert-butyl (2-(3-amino-5-(4-chlorophenoxy)phenoxy)ethyl)carbamate (360.0 mg, 92%).

[0589] LC/MS ESI (+): 379 (M+1)

[0590] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.28 (d, 2H, J=8.9 Hz), 6.96 (d, 2H, J=8.9 Hz), 5.98 (t, 1H, J=2.0 Hz), 5.91-5.94 (m, 2H), 3.92 (t, 2H, J=5.0 Hz), 3.73 (brs, 2H), 3.46-3.50 (m, 2H), 1.44 (s, 9H)

(e) Synthesis of tert-butyl(2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate

[0591] The synthesis procedure of Example 1-h was repeated except for using tert-butyl (2-(3-amino-5-(4-chlorophenoxy)phenoxy)ethyl)carbamate (211.0 mg, 0.56 mmol) as a starting material to obtain tert-butyl (2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate (360.0 mg, 98%) as a white solid.

[0592] LC/MS ESI (+): 682 (M+Na)

[0593] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.53 (brs, 1H), 8.33 (s, 1H), 8.19 (s, 1H), 8.08 (d, 1H, J=8.7 Hz), 7.73 (d, 1H, J=8.7 Hz), 7.47 (d, 2H, J=8.7 Hz), 7.29 (s, 1H), 7.12 (d, 2H, J=8.9 Hz), 7.02-7.04 (m, 2H), 6.44 (s, 1H), 3.94-3.97 (m, 2H), 3.28-3.32 (m, 2H), 2.73 (s, 3H), 1.85 (s, 6H), 1.38 (s, 9H)

Example 94) Synthesis of N-(3-(2-aminoethoxy)-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0594] tert-Butyl (2-(3-(4-chlorophenoxy)-5-(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamido)phenoxy)ethyl)carbamate (187.0 mg, 0.28 mmol) were dissolved in anhydrous CH.sub.2Cl.sub.2 (3.0 mL) and TFA (220.0 μL, 2.84 mmol) was added at 0° C. The reaction mixture was stirred at room temperature for 5 hours, sat. NaHCO.sub.3 was added, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, CH.sub.2Cl.sub.2:MeOH=20:1) to obtain N-(3-(2-aminoethoxy)-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (81.0 mg, 51%) as a white solid.

[0595] LC/MS ESI (+): 559 (M+1)

[0596] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.54 (brs, 1H), 8.35 (s, 1H), 8.20 (s, 1H), 8.09 (d, 1H, J=8.7 Hz), 7.74 (d, 1H, J=8.7 Hz), 7.50 (d, 2H, J=8.7 Hz), 7.32 (s, 1H), 7.12 (d, 2H, J=8.9 Hz), 7.04 (s, 1H), 6.42 (s, 1H), 3.90-3.94 (t, 2H, J=5.6 Hz), 2.87-2.90 (t, 2H, J=5.6 Hz), 2.51 (s, 3H), 2.00 (brs, 2H), 1.85 (s, 6H)

Example 95) Synthesis of N-(5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 3′-chloro-2,4-difluoro-5′-nitro-1,1′-biphenyl

[0597] 1-Bromo-3-chloro-5-nitrobenzene (1.0 g, 4.23 mmol), (2, 4-difluorophenyl)boronic acid (0.7 g, 4.23 mmol), Pd(PPh.sub.3).sub.4 (490.0 mg, 0.42 mmol) and Na.sub.2CO.sub.3 (1.4 g, 12.70 mmol) were added to a mixture of DME/H.sub.2O (42.0 mL, 4/1 v/v). The reaction mixture was stirred at 90° C. for 3 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain 3′-chloro-2,4-difluoro-5′-nitro-1,1′-biphenyl (1.1 g, 96%) as a white solid.

[0598] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.27 (s, 1H), 8.23 (s, 1H), 7.83 (s, 1H), 7.26-7.46 (m, 1H), 6.98-7.03 (m, 2H)

(b) Synthesis of 5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-amine

[0599] The synthesis procedure of Example 1-g was repeated except for using 3′-chloro-2,4-difluoro-5′-nitro-1,1′-biphenyl (1.1 g, 4.08 mmol) as a starting material to obtain 5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-amine (830.0 mg, 85%).

[0600] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.33-7.37 (m, 1H), 6.85-6.93 (m, 3H), 6.68 (m, 2H), 3.81 (brs, 2H)

(c) Synthesis of N-(5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide

[0601] The synthesis procedure of Example 1-h was repeated except for using 5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-amine (40.0 mg, 0.17 mmol) as a starting material to obtain N-(5-chloro-2′,4′-difluoro-[1,1′-biphenyl]-3-yl)-5-((methylsulfonyl)methyl)benzo[b]thiophene-2-carboxamide (30.8 mg, 41%).

[0602] LC/MS ESI (+): 492 (M+1)

[0603] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.76 (s, 1H), 8.40 (s, 1H), 8.11 (d, 1H, J=8.4 Hz), 8.06 (s, 1H), 8.00 (m, 1H), 7.91 (m, 1H), 7.66 (m, 1H), 7.54 (d, 1H, J=8.4 Hz), 7.43 (m, 1H), 7.37 (m, 1H), 7.25 (m, 1H), 4.65 (s, 2H), 2.94 (s, 3H)

Example 96) Synthesis of (8-chloro-6-(4-chlorophenoxy)-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophen-2-yl)methanone

(a) Synthesis of 6-bromo-8-chloro-3,4-dihydro-2H-benzo[b][1,4]oxazine

[0604] 2-Amino-4-bromo-6-chlorophenol (100.0 mg, 0.45 mmol), dibromoethane (0.1 mL, 1.12 mmol) and K.sub.2CO.sub.3(186.0 mg, 1.35 mmol) were dissolved in anhydrous DMF (1.5 mL). The reaction mixture was stirred at 125° C. for 15 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=3:1) to obtain 6-bromo-8-chloro-3,4-dihydro-2H-benzo[b][1,4]oxazine (70.0 mg, 63%) as a white solid.

[0605] LC/MS ESI (+): 248 (M+1)

[0606] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 6.84 (s, 1H), 6.61 (s, 1H), 4.31-4.33 (m, 2H), 3.42-3.45 (m, 2H), 3.97 (brs, 1H)

(b) Synthesis of 8-chloro-6-(4-chlorophenoxy)-3,4-dihydro-2H-benzo[b][1,4]oxazine

[0607] 6-Bromo-8-chloro-3,4-dihydro-2H-benzo[b][1,4]oxazine (60.0 mg, 0.24 mmol), 4-chlorophenol (62 mg, 0.48 mmol), CuI (23.0 mg, 0.12 mmol), N,N-dimethylglycine (24.9 mg, 0.24 mmol) and Cs.sub.2CO.sub.3 (236.0 mg, 0.72 mmol) were added to anhydrous 1,4-dioxane (2.4 mL). The reaction mixture was stirred at 120° C. for 15 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, n-Hex:EtOAc=9:1) to obtain 8-chloro-6-(4-chlorophenoxy)-3,4-dihydro-2H-benzo[b][1,4]oxazine (42.0 mg, 42%).

[0608] LC/MS ESI (+): 296 (M+1)

(c) Synthesis of (8-chloro-6-(4-chlorophenoxy)-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophen-2-yl)methanone

[0609] The synthesis procedure of Example 1-h was repeated except for using 8-chloro-6-(4-chlorophenoxy)-3,4-dihydro-2H-benzo[b][1,4]oxazine (20.0 mg, 0.07 mmol) as a starting material to obtain (8-chloro-6-(4-chlorophenoxy)-2,3-dihydro-4H-benzo[b][1,4]oxazin-4-yl)(5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophen-2-yl)methanone (13.0 mg, 33%) as a white solid.

[0610] LC/MS ESI (+): 576 (M+1)

[0611] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 8.20 (s, 1H), 8.07 (d, 1H, J=8.6 Hz), 7.88 (s, 1H), 7.75 (d, 1H, J=8.7 Hz), 7.02-7.09 (m, 4H), 6.79 (d, 2H, J=8.3 Hz), 4.46-4.51 (m, 2H), 4.10-4.16 (m, 2H), 2.74 (s, 3H), 1.84 (s, 6H)

Example 97) Synthesis of N-(3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of (3-chloro-5-nitrophenyl)(4-chlorophenyl)methanone

[0612] 3-Chloro-5-nitrobenzoic acid (2.0 g, 9.92 mmol) and DMF (0.1 mL, 0.99 mmol) was dissolved in SOCl.sub.2 (3.6 mL, 49.60 mmol). The reaction mixture was stirred at 80° C. for 3 hours and concentrated under reduced pressure to obtain 3-chloro-5-nitrobenzoyl chloride. The residue was dissolved in chlorobenzene (20.0 mL), AlCl.sub.3 (4.0 g, 29.80 mmol) was added at 0° C., and stirred at 50° C. for 5 hours. H.sub.2O was added at 0° C., and the reaction mixture was extracted with EtOAc. The organic extract was washed with sat. NaHCO.sub.3 aqueous solution and brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:DCM=4:1) to obtain (3-chloro-5-nitrophenyl)(4-chlorophenyl)methanone (2.8 g, 96%) as a yellow solid.

[0613] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.46 (m, 1H), 8.44 (m, 1H), 8.08 (m, 1H), 7.75 (d, 2H, J=8.5 Hz), 7.54 (d, 2H, J=8.5 Hz)

(b) Synthesis of 1-chloro-3-(1-(4-chlorophenyl)vinyl)-5-nitrobenzene

[0614] Bromo(methyl)triphenylphosphorane (5.3 g, 19.10 mmol) was dissolved in THF (25.0 mL), 1.6M solution of n-BuLi in n-Hex (12.0 mL, 19.10 mmol) was added dropwise at 0° C., and stirred for 30 minutes. The reaction mixture was slowly added to a solution of (3-chloro-5-nitrophenyl)(4-chlorophenyl)methanone (2.8 g, 9.56 mmol) in THF (8.0 mL) at 0° C. The reaction mixture was stirred at room temperature for 12 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:DCM=4:1) to obtain 1-chloro-3-(1-(4-chlorophenyl)vinyl)-5-nitrobenzene (1.8 g, 65%) as a color solid.

[0615] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.18 (m, 1H), 8.07 (m, 1H), 7.61 (m, 1H), 7.36 (d, 2H, J=8.4 Hz), 7.22 (d, 2H, J=8.4 Hz), 5.63 (s, 1H), 5.60 (s, 1H)

[0616] 1-Chloro-3-(1-(4-chlorophenyl)vinyl)-5-nitrobenzene (1.8 g, 6.19 mmol), CHBr.sub.3 (735.0 μL, 8.42 mmol) and benzyl triethylammonium chloride (254.0 mg, 1.11 mmol) were dissolved in 1,2-dichloroethane (6.2 mL), and NaOH (9.4 g, 235.0 mmol) in H.sub.2O (9.4 mL) was added. The reaction mixture was stirred at 40° C. for 16 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:DCM=4:1) to obtain 1-chloro-3-(2,2-dibromo-1-(4-chlorophenyl)cyclopropyl)-5-nitrobenzene (2.2 g, 75%) as a yellow oil.

[0617] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.22 (s, 1H), 8.11 (s, 1H), 7.79 (s, 1H), 7.44 (d, 2H, J=8.4 Hz), 7.35 (d, 2H, J=8.4 Hz), 2.50-2.55 (m, 2H)

(d) Synthesis of 3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)aniline

[0618] The synthesis procedure of Example 1-g was repeated except for using 1-chloro-3-(2,2-dibromo-1-(4-chlorophenyl)cyclopropyl)-5-nitrobenzene (2.2 g, 4.61 mmol) as a starting material to obtain 3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)aniline (1.2 g, 95%) as a yellow oil.

[0619] LC/MS ESI (+): 278 (M+1)

[0620] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.24 (d, 2H, J=8.4 Hz), 7.15 (d, 2H, J=8.4 Hz), 6.56 (s, 1H), 6.50 (s, 1H), 6.35 (s, 1H), 3.66 (brs, 2H), 1.20-1.28 (m, 4H)

(e) Synthesis of N-(3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)phenyl)-5-(2-(methyl sulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0621] The synthesis procedure of Example 1-h was repeated except for using 3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)aniline (46.7 mg, 0.17 mmol) as a starting material to obtain N-(3-chloro-5-(1-(4-chlorophenyl)cyclopropyl)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (44.1 mg, 47%).

[0622] LC/MS ESI (+): 558 (M+1)

[0623] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.64 (s, 1H), 8.34 (s, 1H), 8.20 (s, 1H), 8.10 (d, 1H, J=8.7 Hz), 7.84 (m, 1H), 7.74 (dd, 1H, J=8.7, 1.8 Hz), 7.54 (m, 1H), 7.38 (d, 2H, J=8.6 Hz), 7.29 (d, 2H, J=8.6 Hz), 7.02 (m, 1H), 2.73 (s, 3H), 1.85 (s, 6H), 1.30-1.32 (m, 4H)

Example 98) Synthesis of N-(3-chloro-5-((2,4-difluorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of N-(3-chloro-5-nitrophenyl)-2,4-difluoroaniline

[0624] 1-Bromo-3-chloro-5-nitrobenzene (100.0 mg, 0.42 mmol), 2,4-difluoroaniline (35.6 pt, 0.35 mmol), Pd.sub.2(dba).sub.3CHCl.sub.3 (18.3 mg, 0.02 mmol), BINAP (21.9 mg, 0.04 mmol) and NaOt-Bu (47.5 mg, 0.49 mmol) were added to anhydrous toluene (3.5 mL). The reaction mixture was allowed to react at 110° C. for 30 minutes in a microwave at 150 W. The reaction mixture was cooled to room temperature, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain N-(3-chloro-5-nitrophenyl)-2,4-difluoroaniline (76.6 mg, 76%) as a yellow solid.

[0625] LC/MS ESI (+): 285 (M+1)

[0626] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.68 (s, 1H), 7.58 (s, 1H), 7.31 (m, 1H), 7.11 (s, 1H), 6.91-7.00 (m, 2H), 5.79 (s, 1H)

(b) Synthesis of N-(3-chloro-5-nitrophenyl)-2,4-difluoro-N-methylaniline

[0627] N-(3-chloro-5-nitrophenyl)-2,4-difluoroaniline (167.1 mg, 0.59 mmol) was dissolved in DMF (6.0 mL), and 60 wt % NaH (35.2 mg, 0.88 mmol) and CH.sub.3I (73.1 μL, 1.17 mmol) were added at 0° C. The reaction mixture was stirred at room temperature for 1 hour, H.sub.2O was added, and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=9:1) to obtain N-(3-chloro-5-nitrophenyl)-2,4-difluoro-N-methylaniline (172.4 mg, 98%) as a yellow solid.

[0628] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.58 (s, 1H), 7.34 (s, 1H), 7.27 (m, 1H), 6.97-7.02 (m, 2H), 6.82 (s, 1H), 3.31 (s, 3H)

[0629] The synthesis procedure of Example 1-g was repeated except for using N-(3-chloro-5-nitrophenyl)-2,4-difluoro-N-methylaniline (172.4 mg, 0.58 mmol) as a starting material to obtain 5-chloro-N.sup.1 (2,4-difluorophenyl)-N.sup.1-methylbenzene-1,3-diamine (148.4 mg, 96%) as a red oil.

[0630] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.22 (m, 1H), 6.87-6.94 (m, 2H), 6.14 (s, 1H), 6.06 (s, 1H), 5.79 (s, 1H), 3.60 (brs, 2H), 3.18 (s, 3H)

(d) Synthesis of N-(3-chloro-5-((2,4-difluorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0631] The synthesis procedure of Example 1-h was repeated except for using 5-chloro-N.sup.1-(2,4-difluorophenyl)-N.sup.1-methylbenzene-1,3-diamine (35.6 mg, 0.13 mmol) as a starting material to obtain N-(3-chloro-5-(2,4-difluorophenyl)(methyl)amino)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (57.2 mg, 79%) as a white solid.

[0632] LC/MS ESI (+): 549 (M+1)

[0633] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.45 (s, 1H), 8.31 (s, 1H), 8.19 (s, 1H), 8.08 (d, 1H, J=8.7 Hz), 7.73 (m, 1H), 7.41-7.53 (m, 3H), 7.21 (m, 1H), 6.93 (s, 1H), 6.48 (s, 1H), 3.23 (s, 3H), 2.72 (s, 3H), 1.84 (s, 6H)

[0634] Compounds from Example 99 and Example 100 were synthesized through the synthesis route of Example 98, data of these compounds are listed as follows.

TABLE-US-00006 TABLE 6 Ex. Compound Analysis data 99 N-(3-chloro-5-((4- LC/MS ESI (+): 547 (M + 1) chlorophenyl)(methyl)amino)phenyl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (2-(methylsulfonyl)propan-2- δ 10.51 (s, 1H), 8.32 (s, 1H), 8.20 (s, 1H), yl)benzo[b]thiophene-2-carboxamide 8.09 (d, 1H, J = 8.7 Hz), 7.74 (dd, 1H, J = 8.7, 1.4 Hz), 7.52 (s, 1H), 7.42 (d, 2H, J = 8.7 Hz), 7.25 (s, 1H), 7.19 (d, 2H, J = 8.7 Hz), 6.73 (s, 1H), 3.27 (s, 3H), 2.73 (s, 3H), 1.85 (s, 6H) 100 N-(2-chloro-6-((4- LC/MS ESI (+): 548 (M + 1) chlorophenyl)(methyl)amino)pyridin-4- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.68 (s, 1H), yl)-5-(2-(methylsulfonyl)propan-2- 8.33 (s, 1H), 8.20 (d, 1H, J = 1.6 Hz), 8.09 (d, yl)benzo[b]thiophene-2-carboxamide 1H, J = 8.7 Hz), 7.74 (dd, 1H, J = 8.7, 1.9 Hz), 7.55 (d, 2H, J = 8.7 Hz), 7.40 (d, 2H, J = 8.7 Hz), 7.33 (d, 1H, J = 1.3 Hz), 6.88 (d, 1H, J = 1.3 Hz), 3.36 (s, 3H), 2.73 (s, 3H), 1.84 (s, 6H)

Example 101) Synthesis of N-(2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 4-amino-6-chloropyridin-2-ol

[0635] 2,6-Dichloropyridine-4-amine (1.0 g, 6.13 mmol) was dissolved in tert-BuOH (30.7 mL) and KOH (516.0 mg, 9.20 mmol) was added. The reaction mixture was stirred at 150° C. for 15 hours, H.sub.2O was added, and extracted with EtOAc. The aqueous layer was acidified with 1N HCl aqueous solution and then extracted with EtOAc. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, MeOH:EtOAc=1:10) to obtain 4-amino-6-chloropyridin-2-ol (120.0 mg, 14%) as an off-white solid.

[0636] LC/MS ESI (+): 145 (M+1)

(b) Synthesis of 4-chlorocyclohex-3-en-1-yl benzoate

[0637] 4-Oxocyclohexyl benzoate (1.1 g, 4.76 mmol) was dissolved in toluene (55.0 mL) and PCl.sub.5 (1.3 g, 6.05 mmol) was added at −40° C. The reaction mixture was stirred at room temperature for 2 hours, H.sub.2O was added, and extracted with EtOAc. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:4) to obtain 4-chlorocyclohex-3-en-1-yl benzoate (850.0 mg, 65%) as an off-white oil.

[0638] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.03 (d, 2H, J=8.0 Hz), 7.57 (t, 1H, J=7.6 Hz), 7.44 (t, 2H, J=7.6 Hz), 5.76 (m, 1H), 5.31 (m, 1H), 2.34-2.61 (m, 4H), 2.05-2.10 (m, 2H)

[0639] 4-Chlorocyclohex-3-en-1-yl benzoate (400.0 mg, 1.69 mmol) was dissolved in MeOH (8.4 mL) and 0.5M solution of NaOMe in MeOH (3.8 mL, 1.86 mmol) was added at 0° C. The reaction mixture was stirred for 2 hours, NaHSO.sub.4 and NaH.sub.2PO.sub.4 buffer solution were added, and extracted with CH.sub.2Cl.sub.2. The organic extract was dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:1) to obtain 4-chlorocyclohex-3-en-1-ol (90.0 mg, 40%) as an off-white oil.

[0640] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 5.69 (m, 1H), 4.01 (m, 1H), 2.41-2.45 (m, 3H), 2.14 (m, 1H), 1.82-1.92 (m, 2H)

(d) Synthesis of 2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridine-4-amine

[0641] 4-Amino-6-chloropyridin-2-ol (80.0 mg, 0.55 mmol) was dissolved in THF (2.0 mL), and 2-4-chlorocyclohex-3-en-1-ol (81.0 mg, 0.61 mmol), 2.2M solution of DEAD in toluene (377.0 μL, 0.83 mmol) and PPh.sub.3 (189.0 mg, 0.72 mmol) were added. The reaction mixture was stirred at room temperature for 15 hours and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, n-Hex:EtOAc=1:2) to obtain 2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridine-4-amine (51.0 mg, 36%) as a yellow oil.

[0642] LC/MS ESI (+): 259 (M+1)

[0643] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 6.21 (s, 1H), 5.82 (s, 1H), 5.72 (m, 1H), 5.27 (m, 1H), 4.14 (s, 2H), 2.43-2.51 (m, 4H), 1.98-2.02 (m, 2H)

(e) Synthesis of N-(2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0644] The synthesis procedure of Example 67-b was repeated except for using 2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridine-4-amine (40.0 mg, 0.15 mmol) as a starting material to obtain N-(2-chloro-6-((4-chlorocyclohex-3-en-1-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (35.0 mg, 42%).

[0645] LC/MS ESI (+): 539 (M+1)

[0646] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.96 (s, 1H), 8.40 (s, 1H), 8.26 (s, 1H), 8.13 (d, 1H, J=8.8 Hz), 7.78 (d, 1H, J=8.8 Hz), 7.46 (s, 1H), 7.24 (s, 1H), 5.81 (m, 1H), 5.21 (m, 1H), 2.75 (s, 3H), 2.43-2.68 (m, 4H), 2.01-2.03 (m, 2H)

Example 102) Synthesis of N-(2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of octahydroindolizin-7-ol

[0647] Hexahydroindolizin-7(1H)-one (220.0 mg, 1.58 mmol) was dissolved in THF (12.5 ml) and 1.0M LiAlH.sub.4 in THF (3.95 ml, 3.95 mmol) was added thereto at room temperature. The mixture was stirred at 80° C. for 30 min. and water was added at 0° C. The resulting reaction mixture was filtered through Celite and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, filtered and evaporated to obtain octahydroindolizin-7-ol (220.0 mg, 99%) as a colorless liquid.

[0648] LC/MS ESI (+): 142 (M+1)

[0649] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 4.63-4.64 (m, 1H), 2.86-2.93 (m, 2H), 1.86-1.97 (m, 3H), 1.56-1.79 (m, 5H), 1.25-1.40 (m, 2H), 0.98-1.07 (m, 1H)

(b) Synthesis of 2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-amine

[0650] Octahydroindolizin-7-ol (200.0 mg, 1.42 mmol) and 2,6-dichloropyridin-4-amine (462.0 mg, 2.83 mmol) were dissolved in sulfolane (7.0 ml) and 60 wt % NaH (113.0 mg, 2.83 mmol) was added thereto at room temperature. The mixture was stirred at 160° C. for 1 hour and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated under a reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain 2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-amine (200.0 mg, 52%) as a colorless liquid.

[0651] LC/MS ESI (+): 268 (M+1)

[0652] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 6.28 (s, 2H), 6.18 (d, 1H, J=1.6 Hz), 5.74-5.76 (m, 1H), 4.72-4.80 (m, 1H), 2.89-3.01 (m, 2H), 2.12-2.16 (m, 1H), 1.86-2.06 (m, 4H), 1.62-1.83 (m, 3H), 1.47-1.56 (m, 1H), 1.27-1.37 (m, 1H), 1.15-1.27 (m, 1H)

(c) Synthesis of N-(2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0653] The synthesis procedure of Example 62-b was repeated except for using 2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-amine (50.0 mg, 0.19 mmol) as a starting material to obtain N-(2-chloro-6-((octahydroindolizin-7-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (11.1 mg, 10%)

[0654] LC/MS ESI (+): 548 (M+1)

[0655] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.95 (s, 1H), 8.40 (s, 1H), 8.26 (d, 1H, J=1.6 Hz), 8.12-8.16 (m, 1H), 7.78 (dd, 1H, J=8.8, 1.6 Hz), 7.45 (d, 1H, J=1.6 Hz), 7.20 (d, 1H, J=1.2 Hz), 4.88-4.94 (m, 1H), 2.94-3.08 (m, 2H), 2.75 (s, 3H), 2.22-2.26 (m, 1H), 1.95-1.96 (m, 4H), 1.79-1.90 (m, 6H), 1.60-1.76 (m, 3H), 1.23-1.42 (m, 3H)

Example 103) Synthesis of N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboximidamide 2,2,2-trifluoroacetate

(a) Synthesis of 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0656] 5-(2-(Methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxylic acid (111.0 mg, 0.37 mmol) was dissolved in CH.sub.2Cl.sub.2 (3.6 mL), and (COCl).sub.2 (50.8 mg, 0.40 mmol) and DMF (cat.) were added dropwise. The reaction mixture was stirred at room temperature for 1 hour and concentrated under reduced pressure to obtain 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carbonyl chloride. The residue was dissolved in 1,4-dioxane (3.7 mL), and 2N solution of NH.sub.3 in MeOH (1.8 mL) was added dropwise. The reaction mixture was stirred at room temperature for 40 minutes, concentrated under reduced pressure. The residue was purified by reversed-phase chromatography (C18-silica gel, CH.sub.3CN:H.sub.2O) to obtain 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (110.0 mg, quant).

[0657] LC/MS ESI (+): 298 (M+1)

[0658] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 8.26 (brs, 1H), 8.11 (d, 1H, J=1.7 Hz), 8.08 (s, 1H), 8.04 (d, 1H, J=8.7 Hz), 7.70 (dd, 1H, J=8.7, 2.0 Hz), 7.66 (brs, 1H), 2.71 (s, 3H), 1.83 (s, 6H)

(b) Synthesis of ethyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carbimidate

[0659] 5-(2-(Methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (85.0 mg, 0.29 mmol) was dissolved in CH.sub.2Cl.sub.2 (6.0 mL) and 1.0M solution of triethyloxonium tetrafluoroborate in CH.sub.2Cl.sub.2 (109.0 mL, 0.57 mmol) was added dropwise. The reaction mixture was stirred at room temperature for 16 hours, and extracted with CH.sub.2Cl.sub.2. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4 and concentrated under reduced pressure. The residue was purified by flash column chromatography (amine silica gel, CH.sub.2Cl.sub.2: MeOH=9:1) to obtain ethyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carbimidate (63.9 mg, 69%).

[0660] LC/MS ESI (+): 326 (M+1)

[0661] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 9.15 (s, 1H), 8.17 (s, 1H), 8.12 (d, 1H, J=1.5 Hz), 8.03 (d, 1H, J=8.7 Hz), 7.70 (dd, 1H, J=8.9, 1.8 Hz), 4.27 (q, 2H, J=7.1 Hz), 2.72 (s, 3H), 1.83 (s, 6H), 1.33 (t, 3H, J=7.1 Hz)

(c) Synthesis of N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboximidamide 2,2,2-trifluoroacetate

[0662] Ethyl 5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carbimidate (63.9 mg, 0.20 mmol) and 3-chloro-5-(4-chlorophenoxy)aniline (59.9 mg, 0.24 mmol) were dissolved in DMF (0.4 mL) and triethylamine (19.9 mg, 0.20 mmol) was added dropwise. The reaction mixture was stirred at 60° C. for 16 hours and then at 100° C. for 16 hours. The reaction mixture was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain N-(3-chloro-5-(4-chlorophenoxy)phenyl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboximidamide 2,2,2-trifluoroacetate (2.4 mg, 2%) as white solid.

[0663] LC/MS ESI (+): 533 (M+1), Free form

[0664] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.79 (brs, 2H), 8.31 (s, 1H), 8.26 (s, 1H), 8.18 (d, 1H, J=7.3 Hz), 7.80 (d, 1H, J=8.6 Hz), 7.49 (d, 2H, J=7.7 Hz), 7.26 (brs, 1H), 7.18 (d, 2H, J=8.4 Hz), 7.14 (brs, 1H), 6.96 (brs, 1H), 2.75 (s, 3H), 1.86 (s, 6H)

Example 104) Synthesis of N-(2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-amine

[0665] 2,6-dichloropyridin-4-amine (50.0 mg, 0.31 mmol) and octahydropyrrolo[1,2-a]pyrazine (77.6 mg, 0.61 mmol) were dissolved in sulfolane (0.5 mL), followed by heating at 150° C. for overnight. Octahydropyrrolo[1,2-c]pyrazine (100.0 mg, 0.80 mmol) was more added. The reaction mixture was stirred at 150° C. for 1 day additionally and then cooled to room temperature and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, CH.sub.2Cl.sub.2:MeOH=7:1) to obtain 2-chloro-6-(hexahydropyrrolo[1,2-c]pyrazin-2(1H)-yl)pyridin-4-amine (66.0 mg, 85%) as a light-yellow amorphous.

[0666] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 6.00 (s, 1H), 5.71 (s, 1H) 4.31 (d, 1H, J=11.9 Hz), 4.07 (d, 1H, J=12.2 Hz), 4.02 (s, 2H), 3.11-3.15 (m, 2H), 2.94-3.01 (m, 1H), 2.57-2.63 (m, 1H), 2.28-2.31 (m, 1H), 2.15-2.19 (m, 1H), 2.03-2.08 (m, 2H), 1.77-1.83 (m, 2H), 1.47-1.50 (m, 1H)

(b) Synthesis of N-(2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0667] The synthesis procedure of Example 62-b was repeated except for using 2-chloro-6-(hexahydropyrrolo[1,2-a]pyrazin-2(1H)-yl)pyridin-4-amine (62.0 mg, 0.25 mmol) to obtain N-(2-chloro-6-(hexahydropyrrolo[1,2-c]pyrazin-2(1H)-yl)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (28.4 mg, 22%).

[0668] LC/MS ESI (+): 533 (M+1)

[0669] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 10.73 (s, 1H), 8.39 (s, 1H), 8.22 (m, 1H), 8.12 (d, 1H, J=8.7 Hz), 7.76 (dd, 1H, J=8.7, 1.8 Hz), 7.22 (s, 1H), 7.13 (s, 1H), 4.23 (d, 1H, J=11.1 Hz), 4.08 (d, 1H, J=12.4 Hz), 3.00-3.09 (m, 2H), 2.87-2.94 (m, 1H), 2.74 (s, 3H), 2.55-2.60 (m, 1H), 2.03-2.16 (m, 2H), 1.86-1.97 (m, 8H), 1.66-1.76 (m, 2H), 1.33-1.43 (m, 1H)

[0670] Compounds from Example 105 and Example 108 were synthesized through the synthesis route of Example 104, data of these compounds are listed as follows.

TABLE-US-00007 TABLE 7 Ex. Compound Analysis data 105 N-(2-(4-(tert-butyl)piperidin-1-yl)- LC/MS ESI (+): 548 (M + 1) 6-chloropyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (methylsulfonyl)propan-2- 10.71 (s, 1H), 8.38 (s, 1H), 8.22 (m, 1H), yl)benzo[b]thiophene-2- 8.11 (d, 1H, J = 8.8 Hz), 7.76 (dd, 1H, carboxamide J = 8.8, 2.0 Hz), 7.17 (s, 1H), 7.09 (s, 1H), 4.24 (d, 2H, J = 12.8 Hz), 2.74-2.79 (m, 5H), 1.85 (s, 6H), 1.74 (d, 2H, J = 11.2 Hz), 1.14-1.26 (m, 3H), 0.85 (s, 9H) 106 N-(2-chloro-6-(octahydro-2H- LC/MS ESI (+): 547 (M + 1) pyrido[1,2-a]pyrazin-2-yl)pyridin- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): 4-yl)-5-(2-(methylsulfonyl)propan- 10.74 (s, 1H), 8.39 (s, 1H), 8.22 (s, 1H), 2-yl)benzo[b]thiophene-2- 8.12 (d, 1H, J = 8.8 Hz), 7.76 (dd, 1H, carboxamide J = 8.8, 1.6 Hz), 7.16 (d, 1H, J = 8.8 Hz), 4.04 (d, 1H, J = 12.4 Hz), 3.92 (d, 1H, J = 11.6 Hz), 2.88-2.94 (m, 1H), 2.81 (dd, 2H, J = 5.6, 0.8 Hz), 2.74 (s, 3H), 2.54-2.57 (m, 1H), 2.12-2.13 (m, 1H), 1.85-1.89 (m, 8H), 1.71-1.77 (m, 1H), 1.59-1.62 (m, 2H), 1.45-1.55 (m, 1H), 1.25-1.30 (m, 3H) 107 N-(2-chloro-6-(7-ethyl-2,7- LC/MS ESI (+): 561 (M + 1) diazaspiro[4.4]nonan-2-yl)pyridin- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): 4-yl)-5-(2-(methylsulfonyl)propan- 10.70 (s, 1H), 8.39 (s, 1H), 8.22 (m, 1H), 2-yl)benzo[b]thiophene-2- 8.12 (d, 1H, J = 8.7 Hz), 7.76 (dd, 1H, carboxamide J = 8.7, 1.9 Hz), 7.02 (m, 1H), 6.90 (m, 1H), 3.36-3.41 (m, 4H), 3.26-3.31 (m, 2H), 2.74 (s, 3H), 2.60-2.67 (m, 1H), 2.39-2.45 (m, 3H), 1.90-2.02 (m, 2H), 1.86 (s, 6H), 1.74-1.79 (m, 2H), 1.02 (t, 3H, J = 7.2 Hz) 108 N-(2-chloro-6- LC/MS ESI (+): 546 (M + 1) (octahydroisoquinolin-2(1H)- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): yl)pyridin-4-yl)-5-(2- 10.70 (s, 1H), 8.40 (s, 1H), 8.23 (m, 1H), (methylsulfonyl)propan-2- 8.13 (d, 1H, J = 8.7 Hz), 7.78 (dd, 1H, yl)benzo[b]thiophene-2- J = 8.7, 1.9 Hz), 7.16 (s, 1H), 7.13 (s, 1H), carboxamide 4.24 (d, 1H, J = 12.4 Hz), 4.04 (d, 1H, J = 12.4 Hz), 2.81-2.87 (m, 1H), 2.75 (s, 3H), 1.87 (s, 6H), 1.70-1.75 (m, 2H), 1.62-1.66 (m, 2H), 1.22-1.31 (m, 3H), 1.10-1.21 (m, 3H), 0.97-1.04 (m, 3H)

Example 109) Synthesis of N-(2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

(a) Synthesis of 4-bromo-2,6-dichloropyridine 1-oxide

[0671] 4-Bromo-2,6-dichloropyridine (5.0 g, 22.04 mmol) was dissolved in TFA (23.8 ml, 309.00 mmol) and H.sub.2O.sub.2 (4.8 ml, 55.10 mmol) was added at room temperature. The mixture was refluxed with stirring at 100° C. for 14 hours, followed by cooling to room temperature and filtered. Filtrate was extracted with EtOAc. The organic extract was washed with 1N NaOH, dried with anhydrous Na.sub.2SO.sub.4, filtered and evaporated to obtain 4-bromo-2,6-dichloropyridine 1-oxide (2.7 g, 49%) as a yellow solid.

[0672] LC/MS ESI (+): 244 (M+1)

[0673] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.61 (s, 2H)

(b) Synthesis of 4-bromo-2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridine 1-oxide

[0674] 4-Bromo-2,6-dichloropyridine 1-oxide (112.0 mg, 0.46 mmol) was dissolved in DMF (4.0 ml) and 5-methylthiazol-2-ol (53.0 mg, 0.46 mmol), Cs.sub.2CO.sub.3 (300.0 mg, 0.92 mmol) were added at room temperature. The mixture was stirred at 40° C. for 2 hours. The reaction mixture was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain 4-bromo-2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridine 1-oxide (50.0 mg, 33%) as a yellow solid.

[0675] LC/MS ESI (+): 321 (M+1)

[0676] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.72 (d, 1H, J=2.8 Hz), 7.67 (d, 1H, J=2.8 Hz), 6.77-6.78 (m, 1H), 2.02 (d, 3H, J=1.6 Hz)

[0677] 4-Bromo-2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridine 1-oxide (40.0 mg, 0.12 mmol) was dissolved in CHCl.sub.3 (1.2 ml) and PCl.sub.3 (33.0 μl, 0.37 mmol) was added thereto at 0° C. The mixture was stirred at room temperature for 6 hours and extracted with EtOAc. The organic extract was washed with 1N NaOH and brine, dried over anhydrous Na.sub.2SO.sub.4, filtered and evaporated to obtain 2-((4-bromo-6-chloropyridin-2-yl)oxy)-5-methylthiazole (35.0 mg, 92%) as an ivory solid.

[0678] LC/MS ESI (+): 305 (M+1)

[0679] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 8.48 (s, 1H), 7.40 (s, 1H), 7.37 (s, 1H), 2.21 (s, 3H)

(d) Synthesis of 2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-amine

[0680] 2-((4-Bromo-6-chloropyridin-2-yl)oxy)-5-methylthiazole (30.0 mg, 0.10 mmol) was dissolved in DMSO (1.0 ml) and Cu.sub.2O (16.9 mg, 0.12 mmol), sodium azide (12.8 mg, 0.20 mmol) were added at room temperature. The mixture was stirred at 100° C. for 1 hour and extracted with EtOAc. The organic extract was washed with brine, dried over anhydrous Na.sub.2SO.sub.4, filtered and concentrated under a reduced pressure. The residue was purified by reversed-phase column chromatography (C18-silica gel, 0.1% formic acid in CH.sub.3CN:0.1% formic acid in H.sub.2O) to obtain 2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-amine (4.0 mg, 16%) as an off-white solid.

[0681] LC/MS ESI (+): 242 (M+1)

[0682] .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 7.48 (d, 1H, J=1.6 Hz), 7.38 (d, 1H, J=1.2 Hz), 6.42 (d, 1H, J=1.6 Hz), 6.44 (brs, 2H), 2.18 (d, 3H, J=1.2 Hz)

(e) Synthesis of N-(2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide

[0683] The synthesis procedure of Example 62-b was repeated except for using 2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-amine (4.0 mg, 0.02 mmol) to obtain N-(2-chloro-6-((5-methylthiazol-2-yl)oxy)pyridin-4-yl)-5-(2-(methylsulfonyl)propan-2-yl)benzo[b]thiophene-2-carboxamide (1.1 mg, 13%) as a white solid.

[0684] LC/MS ESI (+): 522 (M+1)

[0685] .sup.1H-NMR (400 MHz, DMSO-d.sub.6): δ 11.33 (brs, 1H), 8.49 (s, 2H), 8.24 (s, 1H), 8.12 (d, 1H, J=8.8 Hz), 8.00 (d, 1H, J=1.2 Hz), 7.77 (dd, 1H, J=8.8, 1.6 Hz), 7.48 (d, 1H, J=1.2 Hz), 2.74 (s, 3H), 2.22 (d, 3H, J=0.8 Hz), 1.86 (s, 6H)

[0686] Compounds from Example 110 and Example 121 were synthesized through the synthesis route of Example 109, data of these compounds are listed as follows.

TABLE-US-00008 TABLE 8 Ex. Compound Analysis data 110 N-(2-chloro-6-((1-methyl-1H- LC/MS ESI (+): 505 (M + 1) pyrazol-5-yl)oxy)pyridin-4-yl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (2-(methylsulfonyl)propan-2- δ 11.18 (brs, 1H), 8.42 (s, 1H), 8.26 (s, yl)benzo[b]thiophene-2- 1H), 8.13 (d, 1H, J = 8.7 Hz), 7.78 (dd, 1H, carboxamide J = 8.7, 1.9 Hz), 7.72 (d, 1H, J = 1.4 Hz), 7.49 (d, 1H, J = 1.4 Hz), 7.45 (d, 1H, J = 2.0 Hz), 6.09 (d, 1H, J = 2.0 Hz), 3.65 (s, 3H), 2.74 (s, 3H), 1.86 (s, 6H) 111 N-(2-chloro-6-((1,3,5-trimethyl-1H- LC/MS ESI (+): 533 (M + 1) pyrazol-4-yl)oxy)pyridin-4-yl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (2-(methylsulfonyl)propan-2- δ 11.05 (brs, 1H), 8.40 (s, 1H), 8.25 (s, yl)benzo[b]thiophene-2- 1H), 8.13 (d, 1H, J = 8.6 Hz), 7.78 (d, 1H, carboxamide J = 8.6 Hz), 7.67 (s, 1H), 7.22 (s, 1H), 3.69 (s, 3H), 2.74 (s, 3H), 2.09 (s, 3H), 1.96 (s, 3H), 1.86 (s, 6H) 112 N-(2-chloro-6-((1-methyl-1H- LC/MS ESI (+): 505 (M + 1) pyrazol-4-yl)oxy)pyridin-4-yl)-5- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (2-(methylsulfonyl)propan-2- δ 11.08 (brs, 1H), 8.41 (s, 1H), 8.25 (d, yl)benzo[b]thiophene-2- 1H, J = 1.6 Hz), 8.13 (d, 1H, J = 8.8 Hz), carboxamide 7.89 (s, 1H), 7.78 (dd, 1H, J = 8.8, 2.0 Hz), 7.66 (d, 1H, J = 1.2 Hz), 7.49 (s, 1H), 7.33 (d, 1H, J = 0.8 Hz) 3.86 (s, 3H), 2.75 (s, 3H), 1.86 (s, 6H) 113 N-(2-chloro-6-((3,5- LC/MS ESI (+): 520 (M + 1) dimethylisoxazol-4-yl)oxy)pyridin- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): 4-yl)-5-(2-(methylsulfonyl)propan- δ 11.15 (brs, 1H), 8.42 (s, 1H), 8.27 (s, 2-yl)benzo[b]thiophene-2- 1H), 8.15 (d, 1H, J = 8.7 Hz), 7.80 (d, 1H, carboxamide J = 8.7 Hz), 7.68 (s, 1H), 7.47 (s, 1H), 2.75 (s, 3H), 2.32 (s, 3H), 2.10 (s, 3H), 1.87 (s, 6H) 114 N-(2-chloro-6-((5-methylthiophen- LC/MS ESI (+): 521 (M + 1) 3-yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (methylsulfonyl)propan-2- δ 11.10 (brs, 1H), 8.42 (s, 1H), 8.26 (s, yl)benzo[b]thiophene-2- 1H), 8.13 (d, 1H, J = 8.7 Hz), 7.78 (d, 1H, carboxamide J = 8.7 Hz), 7.69 (s, 1H), 7.31 (s, 1H), 7.06 (s, 1H), 6.78 (s, 1H), 2.75 (s, 3H), 2.46 (s, 3H), 1.86 (s, 6H) 115 N-(2-chloro-6-((2-methylthiophen- LC/MS ESI (+): 521 (M + 1) 3-yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (methylsulfonyl)propan-2- δ 11.08 (brs, 1H), 8.41 (s, 1H), 8.26 (s, yl)benzo[b]thiophene-2- 1H), 8.14 (d, 1H, J = 8.7 Hz), 7.79 (d, 1H, carboxamide J = 8.7 Hz), 7.65 (s, 1H), 7.40 (d, 1H, J = 5.4 Hz), 7.27 (s, 1H), 6.93 (d, 1H, J = 5.4 Hz), 2.75 (s, 3H), 2.24 (s, 3H), 1.86 (s, 6H) 116 N-(2-chloro-6-((4,5- LC/MS ESI (+): 520 (M + 1) dimethylisoxazol-3-yl)oxy)pyridin- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): 4-yl)-5-(2-(methylsulfonyl)propan- δ 11.21 (brs, 1H), 8.43 (s, 1H), 8.27 (s, 2-yl)benzo[b]thiophene-2- 1H), 8.14 (d, 1H, J = 8.7 Hz), 7.80 (d, 1H, carboxamide J = 8.7 Hz), 7.75 (s, 1H), 7.59 (s, 1H), 2.75 (s, 3H), 2.39 (s, 3H), 1.87 (s, 6H), 1.76 (s, 3H) 117 N-(2-chloro-6-((5- LC/MS ESI (+): 575 (M + 1) (trifluoromethyl)thiophen-3- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): yl)oxy)pyridin-4-yl)-5-(2- δ 11.14 (brs, 1H), 8.41 (s, 1H), 8.27 (s, (methylsulfonyl)propan-2- 1H), 8.14 (d, 1H, J = 8.7 Hz), 7.81 (m, 2H), yl)benzo[b]thiophene-2- 7.77 (s, 1H), 7.70 (s, 1H), 7.40 (s, 1H), carboxamide 2.75 (s, 3H), 1.87 (s, 6H) 118 methyl 3-((6-chloro-4-(5-(2- LC/MS ESI (+): 550 (M + 1) (methylsulfonyl)propan-2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): yl)benzo[b]thiophene-2- δ 11.20 (brs, 1H), 8.36 (s, 1H), 8.20 (s, carboxamido)pyridin-2- 1H), 8.07 (d, 1H, J = 9.2 Hz), 7.71 (brs, yl)oxy)isoxazole-5-carboxylate 2H), 7.55 (s, 1H), 7.42 (s, 1H), 3.85 (s, 3H), 2.68 (s, 3H), 1.79 (s, 6H) 119 N-(2-chloro-6-((4-methylthiazol-2- LC/MS ESI (+): 522 (M + 1) yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (methylsulfonyl)propan-2- δ 11.63 (brs, 1H), 11.08 (brs, 1H), 8.43 (s, yl)benzo[b]thiophene-2- 1H), 8.27 (d, 1H, J = 1.6 Hz), 8.14 (d, 1H, carboxamide J = 8.8 Hz), 7.85 (s, 1H), 7.77-7.80 (m, 2H), 2.76 (s, 3H), 2.44 (s, 3H), 1.87 (s, 6H) 120 N-(2-chloro-6-((5-methylthiophen- LC/MS ESI (+): 304 (M + 1), 521 (M+3) 2-yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, CDCl.sub.3): δ 11.16 (s, (methylsulfonyl)propan-2- 1H), 8.41 (s, 1H), 8.25 (s, 1H), 8.12 (d, yl)benzo[b]thiophene-2- 1H, J = 9.7 Hz), 7.77 (d, 1H, J = 8.2 Hz), carboxamide 7.71 (s, 1H), 7.42 (s, 1H), 6.64 (s, 2H), 2.74 (s, 3H), 2.41 (s, 3H), 1.85 (s, 6H) 121 N-(2-chloro-6-((2-chlorothiophen- LC/MS ESI (+): 540 (M + 1) 3-yl)oxy)pyridin-4-yl)-5-(2- .sup.1H-NMR (400 MHz, DMSO-d.sub.6): (methylsulfonyl)propan-2- δ 11.20 (brs, 1H), 8.42 (s, 1H), 8.27 (s, yl)benzo[b]thiophene-2- 1H), 8.13 (d, 1H, J = 8.4 Hz), 7.80 (d, 1H, carboxamide J = 9.6 Hz), 7.69 (s, 1H), 7.59 (d, 1H, J = 5.2 Hz), 7.39 (s, 1H), 7.09 (d, 1H, J = 6.0 Hz), 2.74 (s, 3H), 1.86 (s, 6H)

EXPERIMENTAL EXAMPLES

[0687] Experiments were performed as shown below for the compounds prepared in Examples above.

EXPERIMENTAL EXAMPLE 1) EXPERIMENT ON THE INHIBITION OF STAT3 AND STAT1 activities via reporter gene assay

[0688] 1-1) Experiment on the Inhibition of STAT3 Activity

[0689] A human prostate cancer cell line (LNCaP stable cell line; plasmid pSTAT3-TA-luc), which contains a stably operating STAT3 promoter, was cultured in RPMI1640 medium (Cat No. 11875, Life Technologies) containing 10% fetal bovine serum (FBS) (Cat No. SH30396, Thermo Scientific) and 150 μg/mL G-418 solution (Cat No. 04 727 894 001, Roche). The reporter gene assay using LNCaP stable cell line was performed in RPMI1640 medium containing 3% DCC-FBS without G-418 solution. LNCaP stable cells were plated in two (2) white 96-well plates with 30,000 cells/50 μL in each well. The cells were cultured at 37° C., under 5% CO.sub.2 for 24 hours, and then treated with the compounds listed in Examples which were diluted in various concentrations. Subsequently, IL-6 was added to each well with a final concentration of 10 ng/mL. Upon completion of the treatment with the compounds and IL-6, the cells were cultured at 37° C., under 5% CO.sub.2 for 24 hours. The plates were observed under microscope and drug precipitation and particular findings were investigated and recorded.

[0690] The luciferase assay and the cell viability assay were performed respectively with one of the two plates. For the luciferase assay, the liquid media in the 96-well plate was removed, and then, 20 μL, of passive cell lysis buffer was added to each well. After shaking the plate for 30 minutes, luciferase activities of each well were measured in a PHERAstar™ microplate reader (BMG LABTECH) using a luciferase assay system (Cat No. E1501, Promega). For the cell viability assay, the 96-well plate was placed at room temperature for 30 minutes, added with 20 μL/well of CellTiter-Glo solution (Cat No. G7573, Promega), and shaken for 10 minutes in order to measure cytotoxicity caused by the compounds listed in Examples with a PHERAstar™ microplate reader (BMG LABTECH). Wells without 0.1% DMSO and stimulation were used as a negative control and wells with 0.1% DMSO and stimulation were used as a positive control.

[0691] 1-2) Experiment on the Inhibition of STAT1 Activity

[0692] A human osteosarcoma cell line (U2OS stable cell line; pGL4-STAT1-TA-luc), which contains a stably operating STAT1 promoter, was cultured in McCoy 5′A medium (Cat No. 16600, Life Technologies) containing 10% FBS (Cat No. SH30396, Thermo Scientific) and 1000 μg/mL G418 solution (Cat No. 04 727 894 001, Roche). The reporter gene assay using U2OS stable cell line was performed in McCoy 5′A medium containing 10% FBS without G-418 solution. U2OS stable cells were plated in two (2) white 96-well plates with 25,000 cells/50 pt in each well. The cells were cultured at 37° C., under 5% CO.sub.2 for 24 hours, and then treated with the compounds listed in Examples which were diluted in various concentrations. Subsequently, IFN-γ was added to each well with a final concentration of 50 ng/mL. Upon completion of the treatment with the compounds and IFN-γ, the cells were cultured at 37° C., under 5% CO.sub.2 for 8 hours. The plates were observed under microscope and drug precipitation and particular findings were investigated and recorded.

[0693] The luciferase assay and the cell viability assay were performed respectively with one of two plates. For the luciferase assay, the liquid media in the 96-well plate was removed, and then, 20 μL of passive cell lysis buffer was added to each well. After shaking the plate for 30 minutes, luciferase activities of each well were measured in a PHERAstar™ microplate reader (BMG LABTECH) using a luciferase assay system (Cat No. E1501, Promega). For the cell viability assay, the 96-well plate was placed at room temperature for 30 minutes, added with 20 μL/well of CellTiter-Glo solution (Cat No. G7573, Promega), and shaken for 10 minutes in order to measure cytotoxicity caused by the compounds listed in Examples with a PHERAstar™ microplate reader (BMG LABTECH). Wells without 0.1% DMSO and stimulation were used as a negative control and wells with 0.1% DMSO and stimulation were used as a positive control.

[0694] The results of evaluation on the inhibitory effect of the compounds listed in the Examples on the dimerization of STAT3 and STAT1 obtained via the STAT3 and STAT1 reporter gene assays are shown in Table 9 below.

TABLE-US-00009 TABLE 9 IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Ex. pSTAT3 pSTAT1 Ex. pSTAT3 pSTAT1 1 0.0076 >50 2 0.008 >50 3 0.0098 >50 4 0.0091 >50 5 0.028 >50 6 0.019 >50 7 0.0088 >50 8 0.061 >50 9 0.00065 >50 10 0.018 >50 11 0.0021 >50 12 0.0020 >50 13 0.01 >50 14 0.0083 >50 15 0.0057 >50 16 0.0057 >50 17 0.045 >50 18 0.031 >50 19 0.029 >50 20 0.067 >50 21 0.11 >50 22 0.015 >50 23 0.084 >50 24 0.90 >50 25 0.034 >50 26 0.065 >50 27 0.075 >50 28 0.0085 >50 29 0.0041 >50 30 0.0013 >50 31 0.0025 >50 32 0.010 >50 33 0.054 >50 34 8.7 >50 35 0.1 >50 36 0.064 42.1 37 0.015 >50 38 0.018 >50 39 0.0089 >50 40 0.21 >50 41 0.16 >50 42 1.25 >50 43 0.023 >50 44 0.019 >50 45 0.078 >50 46 0.054 >50 47 0.022 >50 48 0.014 >50 49 0.019 >50 50 0.078 >50 51 0.022 >50 52 0.025 >50 53 0.033 >50 54 0.014 >50 55 0.0022 >50 56 3.3 >50 57 0.027 >50 58 0.86 >50 59 0.31 >50 60 0.12 >50 61 0.08 >50 62 0.020 >50 63 0.034 >50 64 0.021 >50 65 0.079 >50 66 0.18 >50 67 0.0084 >50 68 0.011 >50 69 0.010 >50 70 0.024 >50 71 0.011 >50 72 0.01 >50 73 0.13 >50 74 0.12 >50 75 0.24 >50 76 0.39 3.1 77 0.10 >50 78 0.050 >50 79 0.041 >50 80 0.04 >50 81 0.0050 >50 82 0.0058 >50 83 0.0082 >50 84 0.0065 >50 85 0.11 >50 86 0.089 >50 87 0.0097 >50 88 >10 >50 89 0.14 >50 90 0.011 >50 91 0.0051 >50 92 5.5 9.6 93 0.072 >50 94 5.2 13.3 95 0.028 35.7 96 0.19 >50 97 0.025 >50 98 0.031 >50 99 0.11 >50 100 0.07 >50 101 0.0093 >50 102 2.1 14.5 103 0.18 >50 104 1.4 8.7 105 0.049 >50 106 0.43 8.5 107 >10 33.5 108 0.085 >50 109 0.46 >50 110 0.53 44.8 111 1.3 >50 112 0.32 18.9 113 0.18 >50 114 0.063 >50 115 0.019 >50 116 0.20 >50 117 0.028 >50 118 6.0 8.6 119 2.8 12.8 120 0.078 39.6 121 0.027 >50

[0695] As shown in Table 9, the compounds according to the present invention exhibited excellent inhibitory effects against the activity of STAT3 protein but showed almost no inhibitory effect against the activity of STAT1 protein.

Experimental Example 2) Cell Growth Inhibition Assay

[0696] The inhibitory effects of the compounds of the present invention against the growth of cancer cells were evaluated as shown below. The cancer cell lines including prostate cancer cell lines (LNCaP, DU-145), stomach cancer cell line (NCI-N87), and breast cancer cell lines (MDA-MB-468) were cultured under the protocol provided by each supplier. A medium supplemented with 10 ng/mL of IL-6 was used for LNCaP, a prostate cancer cell line, when treated with a drug. Each type of cells to be used in experiments was sub-cultured in a 96-well plate by counting the exact number of cells using Tali™ Image-based Cytometer (Life Technologies). In a 96-well plate, DU-145 was employed with 3,000 cells/well; NCI-N87 was employed with 5,000 cells/well; and LNCaP and MDA-MB-468 were employed with 10,000 cells/well. The cells were treated with the compounds listed in Examples which were diluted in various concentrations. Upon completion of the compounds treatment, LNCaP, DU-145, NCI-N87 cells were cultured at 37° C. under 5% CO.sub.2 for 96 hours, and MDA-MB-468 cells were cultured at 37° C. in air for 96 hours. Subsequently, the cells were observed under microscope and drug precipitation and particular findings were investigated and recorded. And then, the 96-well plate was placed at room temperature for 30 minutes, added with 20 pt/well of CellTiter-Glo solution (Cat No. G7573, Promega) and shaken for 10 minutes, followed by being subjected to the measurement using PHERAstar™ microplate reader (BMG LABTECH) according to the supplier's general luminometer protocol. Wells where only culture liquid added without cell plating were used as a negative control, whereas wells where culture liquid containing 0.1% DMSO instead of the compounds listed in Examples were used as a positive control.

[0697] The results of the inhibitory effects of the compounds prepared in Examples against the growth of cancer cells are shown in Tables 10 to 13 below.

TABLE-US-00010 TABLE 10 IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Ex. LNCap Ex. LNCap Ex. LNCap Ex. LNCap 16 0.0022 17 0.080 18 0.056 19 0.043 21 0.040 22 0.024 23 0.80 24 >1.1 25 0.072 27 0.029 33 0.030 34 >1.1 37 0.01 38 0.0083 41 0.12 42 >1.1 43 0.032 44 0.039 45 0.53 46 0.11 47 0.02 48 0.01 49 0.019 51 0.031 52 0.022 53 0.037 54 0.029 56 >1.1 58 0.24 63 0.046 64 0.013 66 0.26 67 0.047 88 >1.1 89 0.24 92 >1.1 93 0.26 94 >1.1 95 0.023 97 0.028 98 0.031 99 0.14 100 0.14

TABLE-US-00011 TABLE 11 IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Ex. DU-145 Ex. DU-145 Ex. DU-145 Ex. DU-145 16 0.0018 17 0.039 18 0.023 19 0.022 21 0.017 22 0.014 23 0.04 24 >1.1 25 0.066 27 0.024 33 0.023 34 >1.1 37 0.0071 38 0.0053 41 0.063 42 >1.1 43 0.011 44 0.019 45 0.037 46 0.07 47 0.016 48 0.008 49 0.013 51 0.0082 52 0.015 53 0.02 54 0.0059 56 >1.1 58 0.11 63 0.032 64 0.0057 66 0.17 67 0.0053 88 >1.1 89 0.11 92 >1.1 93 0.1 94 >1.1 95 0.013 97 0.016 98 0.0066 99 0.046 100 0.026

TABLE-US-00012 TABLE 12 IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Ex. NCI-N87 Ex. NCI-N87 Ex. NCI-N87 Ex. NCI-N87 9 0.02 10 0.01 11 0.011 12 0.025 13 0.028 14 0.010 15 0.0093 31 0.24 32 0.076 36 0.25 39 0.031 57 0.2 62 0.034 64 0.034 67 0.021 68 0.03 69 0.015 70 0.057 71 0.020 72 0.021 73 0.45 74 0.61 77 0.052 78 0.2 79 0.043 80 0.069 81 0.033 82 0.035 83 0.020 84 0.020 86 0.15 96 1.5 101 0.068 103 1.3 104 1.7 105 0.087 106 1.8 107 5.5 108 0.13 109 1.7 110 1.2 111 2.4 112 1 113 0.27 114 0.13 115 0.14 116 0.91 117 0.037 119 7.8 120 0.12 121 0.15

TABLE-US-00013 TABLE 13 IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) IC.sub.50 (μM) Ex. MDA-MB-468 Ex. MDA-MB-468 Ex. MDA-MB-468 Ex. MDA-MB-468 64 0.0065 71 0.0056 72 0.0040 79 0.0074 80 0.0084 81 0.0038 82 0.0041 83 0.0052 84 0.0026 86 0.024 109 0.068 115 0.021 116 0.062 117 0.0053 119 >0.1 120 0.026 121 0.027

[0698] As shown in Tables 10 to 13, the compounds according to the present invention exhibited excellent inhibitory effects against the growth of various kinds of cancer cells.

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Abstract

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