Acrylamide-Substituted Indane Compounds and Therapeutic Use Thereof

Abstract

The invention relates to indane compounds of formula (I): to their preparation and to their therapeutic use.

##STR00001##

Claims

1. Compound of the formula (I) ##STR00026## wherein R1 is chosen from an oxygen atom, and a group —N(H)— or a group —N(R8)-, wherein R8 is a (C1-C4) alkyl group, in particular a methyl group; R2 is chosen from: a phenyl group unsubstituted or substituted with one or more R4 groups; a benzyl group unsubstituted or substituted with one or more R5 groups; a (C4-C8) cycloalkyl group, in particular a cyclohexyl group or a cyclopentyl group, and more particularly a cyclohexyl group, said (C4-C8) cycloalkyl group being unsubstituted or substituted with one or more R5 groups; a heteroaryl group, in particular a pyridinyl group, said heteroaryl group being unsubstituted or substituted with one or more R5 groups; a (C1-C6) alkyl group, in particular a (C1-C4) alkyl group, said (C1-C6) alkyl group being substituted with one or more fluorine atoms; R4 is chosen from: a halogen atom, in particular a fluorine atom or a chlorine atom; a (C1-C4) alkyl group unsubstituted or substituted with one or more fluorine atoms, in particular a methyl group or a trifluoromethyl group; a (C1-C4) alkoxy group unsubstituted or substituted with one or more fluorine atoms, in particular a methoxy group or a trifluoromethoxy group; and a C(O)—O—(C1-C4) alkyl group, in particular a C(O)—O-methyl group; a (C3-C6) cycloalkyl group; in particular cyclopropyl group; a (C1-C4) alkylthio group; in particular a methylthio group; a pentafluorosulfanyl group; R5 is chosen from a halogen atom, in particular a fluorine atom; and a (C1-C4) alkyl group unsubstituted or substituted with one or more fluorine atoms, in particular a trifluoromethyl group; R3 is chosen from a hydrogen atom, and a (C1-C4) alkyl group, in particular a methyl group; R6 is chosen from a hydrogen atom or a halogen atom, in particular a fluorine atom; R7 is independently chosen from: a halogen atom in particular a fluorine atom; a (C1-C4) alkyl group, in particular a methyl group; a hydroxy group; a (C1-C4) alkoxy group, in particular a methoxy group; n is 0, 1 or 2; or a pharmaceutically acceptable salt thereof.

2. Compound according to claim 1, of the following formula (Ia) ##STR00027## or a pharmaceutically acceptable salt thereof.

3. Compound according to anyone of claim 1 or 2, wherein R3 is a hydrogen atom, or a pharmaceutically acceptable salt thereof.

4. Compound according to anyone of claims 1 to 3, wherein: R1 is an oxygen atom and R2 is chosen from: a phenyl group unsubstituted or substituted with one or more R4 groups; a (C4-C8) cycloalkyl group, in particular a cyclohexyl group, said cycloalkyl group being unsubstituted or substituted with one or more R5 groups; and a (C1-C5) alkyl group, in particular a (C1-C4) alkyl group, said alkyl group being substituted with one or more fluorine atom; especially a (C1-C4) alkyl group, in particular a (C2-C3) alkyl group, substituted with CF3; or R1 is —N(H)— and R2 is chosen from: a phenyl group unsubstituted or substituted with one or more R4 groups; and a heteroaryl group, in particular a pyridinyl group, said heteroaryl group being unsubstituted or substituted with one or more R5 groups; or a pharmaceutically acceptable salt thereof.

5. Compound according to claim 4, wherein: R2 is chosen from: a phenyl group unsubstituted or substituted with one or more R4 groups; a (C4-C8) cycloalkyl group, in particular a cyclohexyl group or a cyclopentyl group, said cycloalkyl group being substituted with one or more R5 groups, provided that R1 is an oxygen atom; and a (C1-C5) alkyl group, in particular a (C1-C4) alkyl group, said alkyl group being substituted with one or more fluorine atom; especially a (C1-C4) alkyl group, in particular a (C2-C3) alkyl group, substituted with CF3; provided that R1 is an oxygen atom; or a pharmaceutically acceptable salt thereof.

6. Compound according to claim 5, wherein R2 is a phenyl group substituted with one or more R4 groups; or a pharmaceutically acceptable salt thereof.

7. Compound according to anyone of claims 4 to 6, wherein R4 is chosen from a halogen atom, in particular a fluorine atom or a chlorine atom and more particularly a fluorine atom; and a (C1-C4) alkyl group unsubstituted or substituted with one or more fluorine atoms, in particular a methyl group or a trifluoromethyl group; or a pharmaceutically acceptable salt thereof.

8. Compound according to anyone of claims 4 to 7, wherein R4 is chosen from a fluorine atom and a trifluoromethyl group, or a pharmaceutically acceptable salt thereof.

9. Compound according to anyone of claims 4 to 8, wherein the R4 group(s) is(are) in the meta and/or para position(s) of the R2 phenyl group, or a pharmaceutically acceptable salt thereof.

10. Compound according to anyone of claim 4 or 5, wherein R5 is chosen from a fluorine atom and a trifluoromethyl group, or a pharmaceutically acceptable salt thereof.

11. Compounds of formula (I) according to claim 1 which are selected from: N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-methyl-N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3-methoxyphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(m-tolylamino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((6-fluoropyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((6-(trifluoromethyl)pyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((5-fluoropyridin-2-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; methyl-3-((5-acrylamido-2,3-dihydro-1H-inden-1-yl)amino)benzoate; N-(3-(benzylamino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((4-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-(((cis)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-(((trans)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-((4,4-difluorocyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-((4,4,4-trifluorobutyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-((3-fluoropropyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4,4,4-trifluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4-fluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((4,4-difluorocyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(((trans)-4-(trifluoromethyl)cyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-phenoxy-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3,4-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3,5-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(2,4-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(3-(trifluoromethoxy)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; methyl 3-[6-(prop-2-enoylamino)-2,3-dihydro-1H-1-yl]oxybenzoate; (S)—N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[2-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-(3-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((3-(pentafluoro-I6-sulfanyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[(1S)-1-[[4-(trifluoromethyl)pyridine-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-[(1R)-1-[[4-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-(1-((4-(trifluoromethyl)pyridin-2-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide 2,2,2-trifluoroacetate; N-(1-((6-(trifluoromethyl)pyridin-2-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-((5-(trifluoromethyl)pyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(methyl(3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(methyl(phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(methyl(4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3,3-dimethyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3,3-dimethyl-1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[7-fluoro-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-[4-fluoro-1-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-methyl-N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((4,4-difluorocyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((3-(trifluoromethyl)cyclopentyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-((5,5,5-trifluoropentyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4,4-difluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(2,2,2-trifluoroethoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3,3,3-trifluoropropoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-methyl-N-(1-((4-(trifluoromethyl)cyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(4-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(m-tolyloxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3-(methylthio)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(3-(3-cyclopropylphenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-methyl-N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; (S)—N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; (R)—N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[3-[[5-(trifluoromethyl)pyridin-2-yl]oxy]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-methyl-N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[2-fluoro-3-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-(2-fluoro-3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[2-fluoro-3-[4-(trifluoromethyl)phenoxy]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-methyl-N-(2-methyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide; N-[(cis)-3-methoxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-[(trans)-2-hydroxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; N-[rac-(2R,3R)-2-hydroxy-3-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide; and the pharmaceutically acceptable salts thereof.

12. Medicament, characterized in that it comprises a compound of formula (I) according to any one of claims 1 to 11, or a pharmaceutically acceptable salt thereof.

13. Pharmaceutical composition, characterized in that it comprises a compound of formula (I) according to any one of claims 1 to 11, or a pharmaceutically acceptable salt thereof.

14. Compound of formula (I) according to any one of claims 1 to 11, for use as an anticancer agent.

15. Compound of formula (I) according to any one of claims 1 to 11, for use in the treatment of breast, ovarian, uterine, prostate, lung, gastric, colorectal, bladder, pancreatic and liver cancers, sarcomas, esophageal, head and neck cancers, uveal melanoma, or glioma.

16. Compound of formula (I) according to any one of claims 1 to 11, for use in the treatment of a patient who has exhibited resistance to prior anti-cancer therapy.

Description

EXAMPLE 1

N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0384] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (151 mg, 751 μmol) was dissolved in AcOEt (8 ml). 3-(trifluoro-methyl)aniline (85 μl, 0.68 mol) and TFA (101 μl, 1.37 mmol) were added. STAB (174 mg, 0.82 mol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at RT. An aqueous solution of NaOH 1N was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 85/15) to obtain 113 mg of N-(1-((3-(trifluoro-methyl)-phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 48%.

EXAMPLES 2 AND 3

Enantiomers 1 and 2 of N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0385] Chiral separation of N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide was realized as follows:

[0386] 100 mg of N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide were dissolved in 10 ml EtOH/heptane 50/50 and purified by reverse chiral phase chromatography (column Chiralcel OD-H 5 μm, 250×30 mm, eluant heptane/EtOH 75/25). Fractions of each enantiomer were combined, evaporated then lyophilized.

[0387] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (41 mg, yield 41%) with 99% e.e.

[0388] OR=+38°, c=2.4 mg/ml DMSO, RT

[0389] A second enantiomer, designated “Enantiomer 2”, was isolated as a white amorphous solid (42 mg, 42%) with 99% e.e.

[0390] OR=−38°, c=2.4 mg/ml DMSO, RT

EXAMPLE 4

N-methyl-N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

Synthesis of N-methyl-N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide

[0391] To a solution of N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (300 mg, 1.49 mmol) in 10 ml anhydrous DMF at 0° C. was added NaH (60% in mineral oil) (60 mg, 1.49 mmol). The temperature was allowed to rise to RT, stirred for 10 min at RT, then cooled down again to 0° C. before adding slowly iodomethane (100 μl, 1.49 mol). The reaction mixture was allowed to rise RT and stirred 1 h at RT. The reaction mixture was cooled to 0° C., ice cold water was added followed by an extraction with AcOEt. Then the combined organic layer was washed with water and an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 80 mg of N-methyl-N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 25%.

Synthesis of N-methyl-N-(1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0392] N-methyl-N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (51 mg, 236 μmol) was dissolved in AcOEt (3 ml). 3-trifluoromethylaniline (27 μl, 215 μmol) and TFA (65 μl, 860 μmol) were added. STAB (110 mg, 516 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 1 h at 40° C. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 21 mg of N-methyl-N-(1-((3-(tri-fluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 25%.

[0393] The following examples were realized by using the appropriate amines in the final reductive amination step 3 of scheme 1 by using the appropriate N-(oxoindany-5-yl)prop-2-enamide as starting material.

EXAMPLE 5

N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0394] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (800 mg, 3.98 mmol) was dissolved in 1,2-dichloroethane (50 ml). 4-fluoroaniline (1.7 ml, 17.9 mmol) and acetic acid (683 μl, 11.9 mmol) were added. STAB (3.8 g, 17.9 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 48 h at RT and 12 h at 40° C. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 369 mg of N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 31%.

EXAMPLES 6 AND 7

Enantiomers 1 and 2 of N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0395] Chiral separation of N-(1-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide was realized as follows:

[0396] 90 mg of N-[1-(4-fluoroanilino)indan-5-yl]prop-2-enamide were dissolved in 8 ml of heptane/EtOH 85/15 and purified by reverse chiral phase chromatography (column Chiralcel OD-H 5 μm, 250×30 mm, eluant heptane/EtOH 85/15). Fractions of each enantiomer were combined, evaporated then lyophilized.

[0397] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (32 mg, yield 36%) with 99.6% e.e.

[0398] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (33 mg, yield 37%) with 99.5% e.e.

EXAMPLE 8

N-(1-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0399] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (360 mg, 1.79 mmol) was dissolved in 1,2-dichloroethane (25 ml). 3-fluoroaniline (776111, 7.9 mmol) and acetic acid (100 μl, 1.79 mmol) were added. STAB (2.2 g, 10 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 30 h at RT and 30 h at 40° C. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. 200 mg of the crude compound was dissolved in 4 ml of MeCN/water 50/50 and purified via a reversed phase chromatography (C18, eluant H.sub.2O (0.1% FA)/MeCN, gradient 20/80 to 0/100). Fractions were combined, evaporated then lyophilized. 59.2 mg of N-(1-((3-fluorophenyl)-amino)-2,3-dihydro-1H-inden-5-yl)acrylamide was isolated as a white lyophilisate, yield 9.4%.

EXAMPLE 9

N-(1-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0400] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 g, 397 μmol) was dissolved in AcOEt (4 ml). 3,5-difluoroaniline (48 mg, 361 μmol) and TFA (54 μl, 721 μmol) were added. STAB (92 mg, 433 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 2 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 7.2 mg of N-(1-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 6%.

EXAMPLE 10

N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0401] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (79 mg, 392 μmol) was dissolved in AcOEt (4 ml). 4-(trifluoromethyl)aniline (45 μl, 356 μmol) and TFA (53 μl, 713 μmol) were added. STAB (91 mg, 428 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 2 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, cyclohexane/AcOEt 100/0 to 90/10) to obtain 20.6 mg of N-(1-((4-(trifluoromethyl)-phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 17%.

EXAMPLE 11

N-(3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0402] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (450 mg, 2.24 mmol) was dissolved in 1,2-dichloroethane (25 ml). 3-(trifluoromethyl)aniline (940 μl, 6.7 mmol) and acetic acid (128 μl, 2.24 mmol) were added. STAB (4.3 g, 20.1 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 120 h at RT and 14 h at 40° C. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 31 mg of N-(3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 4%.

EXAMPLE 12

N-(3-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0403] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80.1 mg, 398 μmol) was dissolved in AcOEt (4 ml). 4-(trifluoromethyl)aniline (46 μl, 322 μmol) and TFA (108 μl, 1.45 mmol) were added. STAB (92 mg, 434 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 24 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromato-graphy (silica gel, gradient cyclohexane/AcOEt 90/10 to 75/25) to obtain 29 mg of N-(3-((4-(trifluoromethyl)phenyl)-amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a yellow foam, yield 23%.

EXAMPLE 13

N-(3-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0404] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 mg, 397 μmol) was dissolved in AcOEt (4 ml). 3,4-difluoroaniline (48 mg, 361 μmol) and TFA (54 μl, 721 μmol) were added. STAB (92 mg, 433 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 2 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 39.4 mg of N-(3-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 34%.

EXAMPLE 14

N-(3-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0405] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (56 mg, 277 μmol) was dissolved in AcOEt (3 ml). 3-fluoroaniline (28 mg, 252 μmol) and TFA (37 μl, 504 μmol) were added. STAB (64 mg, 302 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 4 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, cyclohexane/AcOEt 100/0 to 90/10) to obtain 23.7 mg of N-(3-((3-fluorophenyl)-amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 32%.

EXAMPLE 15

N-(3-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0406] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (56 mg, 277 μmol) was dissolved in AcOEt (3 ml). 4-fluoroaniline (28 mg, 252 μmol) and TFA (37 μl, 504 μmol) were added. STAB (64 mg, 302 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 4 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, cyclohexane/AcOEt 100/0 to 90/10) to obtain 40.2 mg of N-(3-((4-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 54%.

EXAMPLE 16

Synthesis of N-(1-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0407] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 mg, 397 μmol) was dissolved in AcOEt (4 ml). 3,4-difluoroaniline (48 mg, 361 μmol) and TFA (54 μl, 721 μmol) were added. STAB (92 mg, 433 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 2 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 90/10 to 85/15) to obtain 45.6 mg of N-(1-((3,4-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 39%.

EXAMPLE 17

N-(1-((3-methoxyphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0408] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 mg, 398 μmol) was dissolved in AcOEt (4 ml). m-anisidine (42 μl, 362 μmol) and TFA (54 μl, 725 μmol) were added. STAB (92 mg, 435 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 45 mg of N-(1-((3-methoxyphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 39%.

EXAMPLE 18

N-(1-(m-tolylamino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0409] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (81 mg, 400 μmol) was dissolved in AcOEt (4 ml). m-toluidine (39 μl, 364 μmol) and TFA (54 μl, 728 μmol) were added. STAB (93 mg, 437 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 85/15) to obtain 59.6 mg of N-(1-(m-tolylamino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 56%.

EXAMPLE 19

N-(1-((6-fluoropyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0410] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (400 mg, 2 mmol) was dissolved in 1,2-dichloroethane (25 ml). 6-fluoropyridin-3-amine (2 g, 17.9 mmol) and acetic acid (114 μl, 2 mmol) were added. STAB (3.8 g, 17.9 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 72 h at RT and 6 h at 40° C. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromato-graphy (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 12 mg of N-(1-((6-fluoropyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 2%.

EXAMPLE 20

N-(1-((6-(trifluoromethyl)pyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0411] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 mg, 400 μmol) was dissolved in AcOEt (4 ml). 5-amino-2-(trifluoromethyl)pyridine (62 mg, 363 μmol) and TFA (54 μl, 727 μmol) were added. STAB (93 mg, 436 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 75/25) to obtain 54.5 mg of N-(1-((6-(trifluoro-methyl)pyridin-3-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as an colorless oil, yield 41%.

EXAMPLE 21

N-(1-((5-fluoropyridin-2-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0412] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (70 mg, 348 μmol) was dissolved in AcOEt (4 ml). 2-amino-5-fluoropyridine (80 mg, 696 μmol) and TFA (104 μl, 1.39 mmol) were added. STAB (177 mg, 834 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 30 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 50/50) to obtain 10 mg of N-(1-((5-fluoropyridin-2-yl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 9.6%.

EXAMPLE 22

methyl-3-((5-acrylamido-2,3-dihydro-1H-inden-1-yl)-amino)benzoate

[0413] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (80 mg, 400 μmol) was dissolved in AcOEt (4 ml). Methyl 3-aminobenzoate (56 mg, 363 μmol) and TFA (54 μl, 726 μmol) were added. STAB (92 mg, 436 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 30/70) to obtain 66 mg of methyl-3-((5-acrylamido-2,3-dihydro-1H-inden-1-yl)amino)benzoate as a white solid, yield 49%.

EXAMPLE 23

N-(3-(benzylamino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0414] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 994 μmol) was dissolved in THF (8 ml). Benzylamine (330 μl, 3 mmol) and acetic acid (60 mg, 994 μmol) were added. STAB (948 mg, 4.5 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 24 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, cyclohexane/AcOEt 100/0 to 90/10) to obtain 41 mg of N-(3-(benzylamino)-2,3-dihydro-1H-inden-5-yl)-acrylamide as a colorless oil, yield 14%.

EXAMPLE 24

N-(1-((3-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0415] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (160 mg, 795 μmol) was dissolved in 1,2-dichloroethane (15 ml). 3-(trifluoromethyl)benzylamine (233 μl, 1.6 mmol) and acetic acid (46 μl, 795 μmol) were added. STAB (472 mg, 2.2 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 24 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 50 mg of N-(1-((3-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 17%.

EXAMPLE 25

N-(1-((4-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0416] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 994 μmol) was dissolved in 1,2-dichloroethane (20 ml). 4-(trifluoromethyl)benzylamine (161 μl, 1.1 mmol) and acetic acid (58 μl, 0.9 mmol) were added. STAB (608 mg, 2.8 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 72 h at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 73 mg of N-(1-((4-(trifluoromethyl)benzyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 20%.

[0417] Hereinafter are described examples 26 to 29 according to the general scheme 2.

[0418] For examples 26 to 29, commercially available tert-butyl N-(5-aminoindan-2-yl)-carbamate was used to obtain as already described the corresponding tert-butyl N-[5-(prop-2-enoylamino)indan-2-yl]-carbamate which was deprotected as known by people skilled in the art to obtain N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide.

##STR00014##

Synthesis of tert-butyl N-[5-(prop-2-enoylamino)indan-2-yl]carbamate

[0419] tert-butyl N-(5-aminoindan-2-yl)carbamate (400 mg, 1.6 mmol) was dissolved in THF (8 ml). Triethylamine (258 μl, 1.8 mol) was added. The reaction mixture was cooled down to 0° C. before adding slowly acryloyl chloride (146 μl, 1.8 mmol) and stirred at RT for 2 h. The reaction mixture was diluted with AcOEt. A saturated aqueous solution of NaHCO.sub.3 was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 60/40) to obtain 370 mg of tert-butyl N-[5-(prop-2-enoylamino)indan-2-yl]carbamate as a white solid, yield 76%.

Synthesis of N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide

[0420] A suspension of tert-butyl N-[5-(prop-2-enoylamino)indan-2-yl]carbamate (100 mg, 331 μmol) in DCM (6 ml) was cooled down to 0° C. before adding slowly TFA (640 μl, 8.3 mmol) and stirred at RT for 1 h. The reaction mixture was diluted with DCM. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was used for the next step without any purification.

EXAMPLE 26

N-(2-(((cis)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide and

EXAMPLE 27

N-(2-(((trans)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0421] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (90 mg, 445 μmol) was dissolved in DCM (4 ml). Powdered molecular sieves 4 Å, 4-(trifluoromethyl)cyclohexan-1-one (74 mg, 445 μmol) and acetic acid (26 μl, 445 μmol) were added. The reaction mixture was cooled down to 0° C. STAB (142 mg, 668 μmol) was added to the mixture in one portion and stirred overnight. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 50/50) to isolate 43.3 mg of N-(2-(((cis)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid (yield 27%). Further increasing the gradient cyclohexane/AcOEt from 50/50 to 0/100) provided 29.6 mg of N-(2-(((trans)-4-(trifluoromethyl)cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 19%.

EXAMPLE 28

N-(2-((4,4-difluorocyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0422] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (92 mg, 455 μmol) was dissolved in 1,2-dichloroethane (3 ml). Powdered molecular sieves 4 Å, 4,4-difluorocyclohexanone (64 mg, 455 μmol) and acetic acid (30 μl, 455 μmol) were added. The reaction mixture was cooled down to 0° C. and STAB (150 mg, 682 μmol) was added to the mixture in one portion. The reaction mixture was stirred overnight at RT. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 45/55) to obtain 63.4 mg of N-(2-((4,4-difluoro-cyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 43%.

EXAMPLE 29

N-(2-((4,4,4-trifluorobutyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0423] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (104 mg, 514 μmol) was dissolved in DCM (5 ml). 4,4,4-trifluoro-butyraldehyde (68 mg, 514 μmol) and acetic acid (30 μl, 514 μmol) were added. The reaction mixture was cooled down to 0° C. STAB (327 mg, 1.54 mmol) was added to the mixture in one portion and stirred overnight. An aqueous solution of 1N NaOH was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient DCM/MeOH 98/2 to 95/5) to obtain 49.9 mg of N-(2-((4,4,4-trifluorobutyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 32%.

[0424] The following example 30 illustrates an alkylation procedure of the already described N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide by using primary halogenoalkane derivatives.

##STR00015##

EXAMPLE 30

N-(2-((3-fluoropropyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0425] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (108 mg, 532 μmol) was dissolved in acetonitrile (2 ml). Potassium carbonate (149 mg, 1.06 mmol) and 1-bromo-3-fluoro-propane (33 μl, 355 μmol) were added dropwise to the mixture. The 10 ml microwave tube was sealed and the reaction mixture was stirred for 3 h at 80° C. in a sand bath. The solvent was evaporated. Water was added followed by an extraction with DCM. Then the combined organic layer was dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient DCM/MeOH 98/2 to 95/5) to obtain 20.2 mg of N-(2-((3-fluoropropyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 22%.

[0426] The following examples 31 and 32 illustrate the use of the already described N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide under Chan-Lam reaction conditions in order to allow an aryl carbon-heteroatom bond formation via an oxidative coupling of boronic acids with an N—H containing compound in air in the presence of copper(II) salts.

##STR00016##

EXAMPLE 31

N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0427] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (134 mg, 663 μmol) was dissolved in DCM (20 ml). Powdered molecular sieves 4 Å, 3-fluorophenylboronic acid (195 mg, 1.33 mmol), triethylamine (464 μl, 3.31 mmol), and copper (II) acetate (250 mg, 1.33 mmol) were added and stirred at RT for 24 h under oxygene atmosphere. Then the reaction mixture was filtered through celite, the filter pad was washed with DCM. Water was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 80/20) to obtain 24.6 mg of N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 12%.

EXAMPLE 32

N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0428] N-(2-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (67 mg, 331 μmol) was dissolved in DCM (10 ml). Powdered molecular sieves 4 Å, 3-(trifluoromethyl)phenylboronic acid (132 mg, 663 μmop, triethylamine (70 μl, 497 μmop, and copper (II) acetate (94 mg, 497 μmol) were added and stirred at RT for 24 h under oxygene atmosphere. Then the reaction mixture was filtered through celite and the celite pad was washed with DCM. Water was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromato-graphy (silica gel, gradient cyclohexane/AcOEt 90/10 to 50/50) to obtain 10.5 mg of N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 9.2%.

[0429] The following examples 33 to 36 illustrate scheme 1 by exemplifying R1=0 using an alkylation reaction with an alcohol in presence of a strong Lewis acid like boron trifluoride diethyl etherate.

##STR00017##

EXAMPLE 33

N-(3-(4,4,4-trifluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0430] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 0.5 mmol) was solubilized in DCM (15 ml) with 4,4,4-trifluoro-1-butanol (0.2 ml, 1.8 mmol), cooled down to −25° C. before adding boron trifluoride diethyl etherate (0.2 ml, 0.7 mmol) and stirred overnight at RT. 15 ml of a 1M aqueous solution of NaHCO.sub.3 were added, the organic layer was separated, dried over Na.sub.2SO.sub.4 and concentrated under vacuum. The remaining crude product is purified by column chromatography (silica gel, eluant DCM/MeOH 100/0 to 97/3), to obtain 70 mg of N-(3-(4,4,4-trifluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous solid, yield 45%.

EXAMPLE 34

N-(3-(4-fluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide)

[0431] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 0.5 mmol) were solubilized in

[0432] DCM (15 ml) with 4-fluoro-1-butanol (0.16 ml, 1.5 mmol), cooled down to 25° C. before adding boron trifluoride diethyl etherate (0.08 ml, 0.66 mmol) and stirred for 2 h at −25° C., and then overnight at RT. 15 ml of a 1M aqueous solution of NaHCO.sub.3 were added, the organic layer was separated, dried over Na.sub.2SO.sub.4 and concentrated under vacuum. The remaining crude product is purified by column chromatography (silica gel, eluant DCM/MeOH 100/0 to 97/3), to obtain 140 mg N-(3-(4-fluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous solid, yield 76%.

EXAMPLE 35

N-(3-((4,4-difluorocyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0433] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 0.5 mmol) were solubilized in DCM (15 ml) with 4,4-difluorocyclohexan-1-ol (200 mg, 1.5 mmol), cooled down to −25° C. before adding boron trifluoride diethyl etherate (0.1 ml, 0.7 mmol) and stirred for 2 h at −25° C. and overnight at RT. 15 ml of a 1M aqueous solution of NaHCO.sub.3 were added, the organic layer was separated, dried over Na.sub.2SO.sub.4 and concentrated under vacuum. The remaining crude product is purified by column chromatography (silica gel, eluant DCM/MeOH 100/0 to 97/3), to obtain 60 mg of N-(3-((4,4-difluorocyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous solid, yield 38%.

EXAMPLE 36

N-(3-(((trans)-4-(trifluoromethyl)cyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0434] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 0.5 mmol) were solubilized in DCM (15 ml) with 4-trifluoromethyl)cyclohexanol (253 mg, 1.5 mmol), cooled down to −25° C. before adding boron trifluoride diethyl etherate (0.08 ml, 0.66 mmol) and stirred for 2 h at −25° C. and overnight at RT. 15 ml of a 1M aqueous solution of NaHCO.sub.3 were added, the organic layer was separated, dried over Na.sub.2SO.sub.4 and concentrated under vacuum. The remaining crude product is purified by column chromatography (silica gel, eluant DCM/MeOH 100/0 to 97/3), to obtain 41 mg of N-(3-(((trans)-4-(trifluoromethyl)cyclo-hexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous solid, yield 23%.

[0435] The following example 37 illustrates scheme 1 by exemplifying R1=O using a Mitsunobu-approach for the ether bond formation. The indanone-intermediate was reduced to the corresponding secondary alcohol before further derivatization with phenol derivatives.

EXAMPLE 37

N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0436] ##STR00018##

Synthesis of N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide

[0437] 6-aminoindan-1-one (3 g, 20.4 mmol) was dissolved in THF (60 ml) before adding triethylamine (3 ml, 22.4 mmol). The reaction mixture was cooled down to 0° C. before adding slowly acryloyl chloride (1.8 ml, 22.4 mmol) and stirred at RT for 2 h. The reaction mixture was diluted with AcOEt. A saturated aqueous solution of NaHCO.sub.3 was added, followed by an extraction with AcOEt. The combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 40/60) to obtain a yellow solid. This solid was washed with diethyl ether to obtain 3 g of N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide as a yellow solid, yield 73%.

Synthesis of N-(3-hydroxyindan-5-yl)prop-2-enamide

[0438] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (900 mg, 4.5 mmol) was dissolved in methanol (36 ml). The reaction mixture was cooled down to 0° C. before adding sodium borohydride (186 mg, 5 mmol) and stirred at RT for 1 h. The solvent was evaporated. Water was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 50/50) to obtain 809 mg of N-(3-hydroxyindan-5-yl)prop-2-enamide as a white solid, yield 89%.

Synthesis of N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0439] N-(3-hydroxyindan-5-yl)prop-2-enamide (215 mg, 1 mmol) was dissolved in THF (12 ml). 4-(trifluoromethyl)phenol (206 mg, 1.3 mmol) and triphenylphosphane (332 mg, 1.3 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (250 μl, 1.3 mmol) and stirred at RT for 4 h. The solvent was evaporated and the crude product was pre-purified by column chromatography (silica gel, gradient cyclo-hexane/AcOEt 100/0 to 90/10), followed by a second column chromatography with a less polar gradient (silica gel, gradient DCM/AcOEt 100/0 to 99/1) to obtain 140 mg of N-(3-(4-(trifluoromethyl)-phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 38%.

[0440] The following examples were realized as described before.

EXAMPLE 38

N-(3-phenoxy-2,3-dihydro-1H-inden-5-yl)acrylamide

[0441] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (180 mg, 886 μmol) was dissolved in THF (10 ml). Phenol (94 μl, 1.1 mmol) and triphenylphosphane (284 mg, 1.1 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (213 μl, 1.1 mmol) at RT for 4 h. The solvent was purified by reverse phase chromatography (column CSH 250 mm×5 mm, eluant H.sub.2O (0.1% FA)/MeCN (0.1% FA), gradient 74/26 to 5/95) to obtain 23 mg of N-(3-phenoxy-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 9.3%.

EXAMPLE 39

N-(3-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0442] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (300 mg, 1.5 mmol) was dissolved in THF (14 ml). 3-(trifluoromethyl)phenol (218 μl, 1.8 mmol) and triphenylphosphane (474 mg, 1.8 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (356 μl, 1.8 mmol) and stirred at RT for 4 h. The solvent was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 70/30) and by a second column chromatography (silica gel, gradient cyclohexane/DCM 100/0 to 35/65) to obtain 34.2 mg of N-(3-(3-(trifluoro-methyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 6.7%.

EXAMPLE 40

N-(3-(3,4-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0443] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 984 μmol) was dissolved in THF (12 ml). 3,4-difluorophenol (157 mg, 1.2 mmol) and triphenylphosphane (310 mg, 1.2 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (233 μl, 1.2 mmol) and stirred at RT for 4 h. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 85/15), then by column chromatography (silica gel, gradient DCM/AcOEt 100/0 to 99/1) to obtain 33 mg of N-(3-(3,4-difluoro-phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 10%.

EXAMPLE 41

N-(3-(3-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0444] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (150 mg, 738 μmol) was dissolved in

[0445] THF (8 ml). 3-fluorophenol (80 μl, 886 μmol) and triphenylphosphane (232 mg, 886 μmop were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (174 μl, 886 μmol) and stirred at RT for 4 h. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 85/15) to obtain 250 mg which were solubilized in 10 ml MeCN/H.sub.2O 50/50 and further purified by reverse phase chromatography (column CSH 250 mm×5 mm 5 μm, eluant H.sub.2O (0.1% FA)/MeCN (0.1% FA), gradient 66/34 to 56/54) to obtain 51 mg of N-(3-(3-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white lyophilisate, yield 23%.

EXAMPLE 42

N-(3-(4-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0446] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (150 mg, 738 μmol) was dissolved in THF (8 ml), 4-fluorophenol (99 mg, 886 μmol) and triphenylphosphane (237 mg, 886 μmop were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (176 μl, 886 μmol) and stirred at RT for 24 h. The solvent was evaporated. 955 mg of the crude product was dissolved in 18 ml of (6 ml MeCN/12 ml MeOH) and purified by reverse phase chromatography (H.sub.2O (0.1% FA)/MeCN, gradient 63/37 to 0/100). Fractions were combined, evaporated then lyophilized. 29.6 mg of N-(3-(4-fluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide was isolated as a white lyophilisate, yield 14%.

EXAMPLE 43

N-(3-(3,5-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0447] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (150 mg, 738 μmol) was dissolved in THF (8 ml). 3.5-difluorophenol (115 mg, 886 μmol) and triphenylphosphane (237 mg, 886 μmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (176 μl, 886 μmol) and stirred at RT for 24 h. The solvent was evaporated. 1.1 g of the crude product was dissolved in 7 ml of MeOH and purified by reverse phase chromatography (H.sub.2O (0.1% FA)/MeCN, gradient 68/32 to 0/100). Fractions were combined, evaporated then lyophilized. 12 mg of N-(3-(3,5-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide was isolated as a white lyophilisate, yield 5.2%.

EXAMPLE 44

N-(3-(2,4-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0448] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (150 mg, 738 μmol) was dissolved in THF (8 ml). 2.4-difluorophenol (86 μl, 886 μmol) and triphenylphosphane (237 mg, 886 μmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (176 μl, 886 μmol) and stirred at RT for 24 h. The solvent was evaporated. 1 g of the crude product was dissolved in 12 ml of MeOH and purified by reverse phase chromato-graphy (H.sub.2O (0.1% FA)/MeCN, gradient 67/33 to 0/100). Fractions were combined, evaporated then lyophilized. 41.7 mg of N-(3-(2,4-difluorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide was isolated as a yellow lyophilisate, yield 18%.

EXAMPLE 45

N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0449] N-(1-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (60 mg, 295 μmol) was dissolved in THF (5 ml). 3-(trifluoromethyl)phenol (44 μl, 354 μmol) and triphenylphosphane (95 mg, 354 μmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (71 μl, 354 μmol) and stirred at RT for 24 h. The solvent was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 90/10), then by a subsequent column chromatography (silica gel, gradient DCM/AcOEt 100/0 to 99/1) to obtain 19 mg of N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 18%.

EXAMPLE 46

N-(1-(3-(trifluoromethoxy)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0450] N-(1-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (250 mg, 1.23 mmol) was dissolved in DCM (14 ml). 3-(trifluoromethoxy)phenol (191 μl, 1.5 mmol) and triphenylphosphane (395 mg, 1.5 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (293 μl, 1.5 mmol) and stirred at RT for 3 h. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 85/15), then by column chromatography (silica gel, gradient DCM/AcOEt 100/0 to 99/1) to obtain 170 mg of N-(1-(3-(trifluoromethoxy)-phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 38%.

EXAMPLE 47

methyl 3-[6-(prop-2-enoylamino)-2,3-dihydro-1H-inden-1-yl]oxybenzoate

[0451] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (500 mg, 2.4 mmol) was dissolved in THF (12 ml). methyl 3-hydroxybenzoate (458 mg, 3 mmol) and triphenylphosphane (790 mg, 3 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (595 mg, 3 mmol) and stirred at RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) and further via reverse phase chromatography (C18 5 μm OBD 50×250 mm, eluant H.sub.2O (0.1% FA)/MeCN, gradient from 67/33 to 0/100) to obtain 106 mg methyl 3-[6-(prop-2-enoylamino)-indan-1-yl]oxybenzoate as a white foam, yield 13%.

EXAMPLES 48 AND 49

Enantiomers 1 and 2 of N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0452] Chiral separation of N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide (example 31) was realized as follows:

[0453] 570 mg of N-(2-((3-fluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide were dissolved in 50 ml of heptane/EtOH 80/20 and purified by reverse chiral phase chromatography (column Chiralcel OD-I 20 μm, 350×76 mm, eluant heptane/EtOH 80/20). Fractions of each enantiomer were combined and evaporated.

[0454] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (254 mg, yield 45%) with 99.5% e.e.

[0455] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (237 mg, yield 42%) with 99.5% e.e.

EXAMPLES 50 AND 51

Enantiomers 1 and 2 of N-(2-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0456] Chiral separation of N-(2-((3-trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide (example 32) was realized as follows:

[0457] 360 mg of N-(2-((3-trifluoromethylphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide were dissolved in 50 ml of heptane/EtOH 85/15 and purified by reverse chiral phase chromatography (column Chiralcel OD-I 20 μm, 350×76 mm, eluant heptane/EtOH 85/15, 400 ml/min). Fractions of each enantiomer were combined and evaporated, then lyophilized.

[0458] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (157 mg, yield 44%) with 99.5% e.e.

[0459] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (156 mg, yield 43%) with 99.5% e.e.

EXAMPLE 52

N-[2-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0460] To a solution of N-(2-aminoindan-5-yl)acrylamide (TFA salt) (105 mg, 331 μmol) in DCM (5 ml) and powdered molecular sieves 4 Å were added successively 4-(trifluoromethyl)-phenylboronic acid (126 mg, 661 μmop, triethylamine (500 μl, 3.307 mmol) and copper(II)acetate (120 mg, 661 μmol). The reaction mixture was stirred for 1 h at RT. After filtration on Dicalite, water and a few drops of an aqueous solution of NH.sub.3 (33%) were added, followed by an extraction with DCM. Then the combined organic layer was washed with water and brine, filtered on a hydrophobic cartridge and concentrated at reduced pressure. The crude product was purified by column chromatography (SiO.sub.2, cyclo-hexane/AcOEt 90/10 to 50/50) and a second column chromatography (SiO.sub.2, DCM/AcOEt 100/0 to 90/1) to obtain 26 mg of N-[2-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide as white solid, yield 23%.

EXAMPLE 53

N-(3-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0461] N-(3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (81 mg, 405 μmol) was dissolved in AcOEt (4 ml), 3,5-difluoroaniline (47 mg, 368 μmol) and TFA (54 μl, 736 μmol) were added. STAB (94 mg, 442 μmol) was added to the mixture in one portion. The reaction mixture was stirred at 25° C. overnight. An aqueous solution of NaOH 1N (10 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by two subsequent identic column chromatographies (silica gel, gradient cyclohexane/AcOEt 90/10 to 50/5) to obtain 60 mg of a white foam, which was further purified by reverse phase chromatography (column WATERS Xselect CSH Prep C18 5 μm OBD, 50×250 mm, mobile phase A: H.sub.2O+0.1% FA/B: MeCN, gradient 63/37 to 8/92) to obtain after lyophilization 16 mg of a white foam of N-(3-((3,5-difluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide, yield 15%.

EXAMPLE 54

N-(1-((3-(pentafluoro-I6-sulfanyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0462] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (725 mg, 3.57 mmol) was dissolved in AcOEt (20 ml) with powdered molecular sieves 4 Å 3-(pentafluoro-I6-sμlfanyl)aniline (740 mg, 3.21 mmol), then TFA (495 μl, 6.40 mmol) were added. STAB (2.5 g, 7.8 mmol) was added to the mixture in two portions. The reaction mixture was stirred at 60° C. overnight. After filtration on Dicalite, the pH was adjusted to pH8 by adding an aqueous solution of NaOH 1N, followed by an extraction with DCM, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/40) to obtain after trituration in diisopropylether 460 mg N-(1-((3-(pentafluoro-I6-sulfanyl)phenyl)amino)-hydro-1H-inden-5-yl)acrylamide as a white solid, yield 35%.

EXAMPLES 55 AND 56

Enantiomers 1 and 2 of N-(1-((4-(trifluoromethyl)phenyl)amino)-hydro-1H-inden-5-yl)acrylamide

[0463] Chiral separation of N-(1-((4-trifluoromethylphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide (example 10) was realized as follows:

[0464] 400 mg of N-(1-((4-trifluoromethylphenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide were dissolved in 100 ml of heptane/EtOH 80/20 and purified by reverse chiral phase chromatography (Chiralpak AY 20 μm, 230×100 mm, eluant heptane/EtOH 80/20 to 50/50, 400 ml/min). Fractions of each enantiomer were combined and evaporated, then lyophilized.

[0465] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (191 mg, yield 48%) with 99.5% e.e.

[0466] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (183 mg, yield 46%) with 99.5% e.e.

EXAMPLES 57 AND 58

Enantiomers 1 and 2 of N-1-[[4-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0467] Chiral separation of N-1-[[4-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide (example 59 below) was realized as follows:

[0468] 236 mg of N-1-[[4-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide were dissolved in two portions of 100 ml of heptane/EtOH 80/20 and purified by reverse chiral phase chromatography (Chiralpak AY 20 μm, 230×100 mm, eluant heptane/EtOH 80/20 to 50/50, 400 ml/min). Fractions of each enantiomer were combined and evaporated, then lyophilized.

[0469] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (100 mg, yield 42%) with 99% e.e.

[0470] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (101 mg, yield 46%) with 99% e.e.

EXAMPLE 59

N-[1-[[4-(trifluoromethyl)pyrimidin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide TFA salt

[0471] To a suspension of N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (1.12 g, 5.29 mmol), molecular sieves (4 Å) and 4-(trifluoromethyl)pyridin-2-amine (0.8 g, 4.79 mmol) in AcOEt (30 ml), TFA (750 μl, 9.37 mmol) was added. After 10 minutes of stirring at RT, STAB (2.52 g, 11.54 mmol) was slowly added to the mixture (by portions). The reaction mixture was heated at reflux overnight. After cooling, the reaction mixture was filtered over dicalite, diluted with an aqueous solution of NaOH 1N followed by an extraction with AcOEt. Then the combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 60/40) followed by a reverse phase chromatography (C18, gradient MeCN/H.sub.2O+0.1% TFA) to obtain after crystallization in diisopropyl ether 70 mg of N-[1-[[4-(trifluoromethyl)-2-pyridyl]-amino]-2,3-dihydro-1H-inden-5-yl]acrylamide TFA salt as a white solid, yield 3.1%.

EXAMPLE 60

N-[1-[[6-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0472] To a suspension of N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (1.1 g, 4.7 mmol), molecular sieves (4 Å) and 6-(trifluoromethyl)pyridin-2-amine (0.8 g, 4.69 mmol) in AcOEt (30 ml), TFA (750 μl, 9.37 mmol) was added. After 10 minutes stirring at RT, STAB (2.52 g, 11.54 mmol) was slowly added to the mixture (by portions). The reaction mixture was heated at reflux overnight. After cooling, the reaction mixture was filtered over dicalite and an aqueous solution of NaOH 1N was added to the filtrate, followed by an extraction with AcOEt. Then the combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude product was purified twice by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to yield after crystallization in a mixture of diisopropylether/heptane 1/1 133 mg of N-[1-[[6-(trifluoromethyl)pyridin-2-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white solid, yield 8%.

EXAMPLE 61

N-[1-[[5-(trifluoromethyl)pyridin-3-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0473] To a suspension of N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (1.1 g, 4.7 mmol), molecular sieves (4 Å) and 5-(trifluoromethyl)pyridin-3-amine (0.8 g, 4.69 mmol) in AcOEt (30 ml), TFA (720 μl, 9.31 mmol) was added. After 10 minutes stirring at RT, STAB (2.52 g, 11.54 mmol) was slowly added to the mixture (by portions). The reaction mixture was allowed to reflux overnight. After cooling, the reaction mixture was filtered over Dicalite and an aqueous solution of NaOH 1N was added to the filtrate, followed by an extraction with AcOEt. Then the combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated under vacuum. The crude product was purified twice by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 60/40) followed by a reverse phase chromatography (C18, gradient MeCN/H.sub.2O+0.1% FA) to obtain after cristallisation in a mixture of diisopropyl-ether/heptane 1/1 72 mg of N-[1-[[5-(trifluoromethyl)pyridin-3-yl]amino]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white solid, yield 4.4%.

EXAMPLE 62

N-(1-(methyl(3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0474] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (250 mg, 1.24 mmol) was dissolved in AcOEt (8 ml), N-methyl-3-(trifluoromethyl)aniline (162 μl, 1.24 mmol) and TFA (283 μl, 3.73 mmol) were added. STAB (474 mg, 2.24 mmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at 35° C. An aqueous solution of NaOH 1N (20 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 200 mg N-(1-(methyl(3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 45%.

EXAMPLE 63

N-(1-(methyl(phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0475] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 497 μmol) was dissolved in AcOEt (4 ml). N-methyl aniline (51 μl, 452 μmol) and TFA (69 μl, 904 μmol) were added. STAB (120 mg, 543 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at 35° C. An aqueous solution of NaOH 1N (10 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 60 mg of N-(1-(methyl(phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 45%.

EXAMPLE 64

N-(1-(methyl(4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0476] N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (250 mg, 1.26 mmol) was dissolved in AcOEt (8 ml). N-methyl-4-(trifluoromethyl)aniline (162 μl, 1.14 mmol) and TFA (260 μl, 3.43 mmol) were added. STAB (435 mg, 2.06 mmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at 35° C. An aqueous solution of NaOH 1N was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 158 mg N-(1-(methyl(4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 38%.

EXAMPLE 65

N-(3,3-dimethyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0477] N-(3,3-dimethyl-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (93 mg, 406 μmol) was dissolved in AcOEt (4 ml). 3-(trifluoromethyl)aniline (47 μl, 367 μmol) and TFA (90 μl, 1.11 mmol) were added. STAB (120 mg, 553 μmol) was added to the mixture in several portions. The reaction mixture was stirred for 4 h at RT. An aqueous solution of NaOH 1N (10 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 26 mg of N-(3,3-dimethyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a yellow gum, yield 19%.

EXAMPLE 66

N-(3,3-dimethyl-1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0478] N-(3,3-dimethyl-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (71 mg, 308 μmol) was dissolved in AcOEt (4 ml). 4-(trifluoro-methyl)aniline (108 μl, 923 μmol) and TFA (130 μl, 1.8 mmol) were added. STAB (220 mg, 1.11 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 5 h at 40° C. An aqueous solution of NaOH 1N (10 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 53 mg of N-(3,3-dimethyl-1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 51%.

EXAMPLE 67

N-[7-fluoro-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0479] N-(7-fluoro-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (280 mg, 1.2773 mmol) was dissolved in AcOEt (12 ml), 3-(trifluoromethyl)aniline (160 μl, 1.2773 mmol) and TFA (160 μl, 2.5546 mmol) were added. STAB (324.86 mg, 1.5328 mmol) was added to the mixture in one portion. The reaction mixture was stirred for 2 h at 40° C. As all of the solid was not solubilized, additional TFA (100 μl, 1 eq) was added and stirring at 40° C. was continued for 5 h.

[0480] An aqueous solution of NaOH 1N (20 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 182 mg N-[7-fluoro-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white foam, yield 39%.

EXAMPLE 68

N-[4-fluoro-1 [4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0481] N-(4-fluoro-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (130 mg, 0.93 mmol) was dissolved in AcOEt (6 ml), 4-(trifluoromethyl)aniline (74 μl, 0.93 mmol) and TFA (273 μl, 3.53 mmol) were added. STAB (453 mg, 2.136 mmol) was added to the mixture in several portions. The reaction mixture was stirred for 6 h at 40° C. An aqueous solution of NaOH 1N was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclo-hexane/AcOEt 100/0 to 50/50) to obtain 58 mg N-[4-fluoro-1-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white foam, yield 27%.

EXAMPLE 69

N-methyl-N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0482] N-(1-((4-trifluoromethyl)phenyl)amino-2,3-dihydro-1H-inden-5-yl)acrylamide (30 mg, 87 μmol) was dissolved in MeCN (1 ml). Cesium carbonate (56 mg, 173 μmol) was added followed by iodomethane (27 μl, 433 μmol). The reaction mixture was stirred for 2 h at 80° C. Water was added, followed by an extraction with AcOEt, the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 40/60) to obtain 10 mg of N-methyl-N-(1-((4-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 32%.

EXAMPLE 70

N-(3-((4,4-difluorocyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0483] N-(3-amino-2,3-dihydro-1H-inden-5-yl)acrylamide (30 mg, 148 μmol) was dissolved in DCM (3 ml) with 4,4-difluorocyclohexan-1-one (22 mg, 163 μmop, AcOH (9 μl, 163 μmop and powdered molecular sieves 4 Å. Then STAB (50 mg, 223 μmol) was added and the reaction mixture was stirred for 24 h at RT. After filtration on Dicalite, an aqueous solution of NaOH 1N (5 ml) was added, followed by an extraction with DCM. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 10 mg of N-(3-((4,4-difluorocyclohexyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 20%.

EXAMPLE 71

N-(3-((3-(trifluoromethyl)cyclopentyl)oxy)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0484] To a solution of N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 1.0 mmol) and 3-(trifluoromethyl)cyclopentan-1-ol (455 mg, 3.00 mmol) in DCM (15 ml) was added boron trifluoride diethyl etherate (0.2 ml, 1.40 mmol) at 0° C., and the mixture was stirred at 0° C. for 2 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/AcOEt, 100/0 to 97/3) to obtain of a mixture of diastereoisomers (LCMS 85/15%). This crude product was purified by SFC (column IA: 250 mm*30 mm; mobile phase: [A: CO.sub.2, B: MeOH/0.1% DEA] to obtain 100 mg of a colorless resin N-(3-((3-(trifluoromethyl)cyclopentyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide, yield 30%.

EXAMPLE 72

N-(3-((5,5,5-trifluoropentyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0485] To a solution of N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 0.5 mmol) and 5,5,5-trifluoropentan-1-ol (420 mg, 3 mmol) in DCM (15 ml) at 0° C. was added boron trifluoride diethyl etherate (0.2 ml, 1.4 mmol). The mixture was stirred at 0° C. for 2 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/AcOEt, 100/0 to 99/1) to obtain 170 mg of N-(3-((5,5,5-trifluoropentyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as white solid, yield 53%.

EXAMPLE 73

N-(3-(4,4-difluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0486] To a solution of N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (134 mg, 0.64 mmol) and 4,4-difluorobutan-1-ol (230 mg, 1.98 mmol) in DCM (15 ml) at 0° C. was added boron trifluoride diethyl etherate (0.127 ml, 0.99 mmol). The mixture was stirred at 0° C. for 2 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/MeOH, 100/0 to 99/1) to obtain 65 mg of N-(3-(4,4-difluorobutoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 33%.

EXAMPLE 74

N-(3-(2,2,2-trifluoroethoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0487] To a solution of N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (130 mg, 0.64 mmol) and 2,2,2-trifluoroethanol (0.142 ml, 1.92 mmol) in DCM (15 ml) at 0° C. was added boron trifluoride diethyl etherate (0.123 ml, 0.96 mmol). The mixture was stirred at 0° C. for 2 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/MeOH, 100/0 to 99/1) to obtain 30 mg of N-(3-(2,2,2-trifluoroethoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 16%.

EXAMPLE 75

N-(3-(3,3,3-trifluoropropoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0488] To a solution of N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 0.5 mmol) and 4-fluoro-1-butanol (0.160 ml, 1.9 mmol) in DCM (15 ml) at 0° C. was added boron trifluoride diethyl etherate (0.080 ml, 1.5 mmol). The mixture was stirred at 0° C. for 5 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/MeOH, 100/0 to 99/1) to obtain 70 mg of N-(3-(2,2,2-trifluoropropoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white powder, yield 47%.

EXAMPLE 76

N-methyl-N-(1-((4-(trifluoromethyl)cyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0489] To a solution of N-(1-hydroxy-2,3-dihydro-1H-inden-5-yl)-N-methylacrylamide (53 mg, 0.24 mmol) and 4-(trifluoromethyl)cyclohexanol (0.10 ml, 0.73 mmol) in DCM (5 ml) at 0° C. was add boron trifluoride diethyl etherate (0.04 ml, 0.34 mmol). The mixture was stirred at 0° C. for 2 h. An aqueous solution of NaHCO.sub.3 1N was added, the organic phase was separated, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The residue was purified by column chromatography (SiO.sub.2, DCM/MeOH, 100/0 to 99/1) to obtain 39 mg of an isomeric mixture (74/26) of N-methyl-N-(1-((4-(trifluoromethyl)cyclohexyl)oxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless gum, yield 47%.

EXAMPLE 77

N-(3-(4-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0490] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (217 mg, 1.07 mmol) was dissolved in DCM (15 ml) under N.sub.2. 4-chlorophenol (168 mg, 1.28 mmol) and triphenylphosphane (343 mg, 1.28 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (255 μl, 1.28 mmol) solubilized in DCM (5 ml) and stirred 20 min at 0° C. then RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient DCM/AcOEt 100/0 to 98/2) and reverse phase chromatography (column: Phenomenex Gemini-NX C18 75×30 mm 3 μm; mobile phase: [A: H.sub.2O (0.225% FA) B: MeCN]; gradient B %: 50%-80%, 7 min) to obtain 17 mg of N-(3-(4-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white foam, yield 5%.

EXAMPLE 78

N-(3-(3-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0491] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (214 mg, 1.05 mmol) was dissolved in DCM (15 ml) under N.sub.2. 3-chlorophenol (130 μl, 1.26 mmol) and triphenylphosphane (343 mg, 1.28 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (251 μl, 1.28 mmol) solubilized in DCM (5 ml) and stirred 20 min at 0° C. and then at RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient DCM/AcOEt 100/0 to 98/2) and reverse phase chromatography (column: Phenomenex Gemini-NX C18 75×30 mm 3 μm; mobile phase: [A: H.sub.2O (0.225% FA) B: MeCN]; gradient B %: 50%-80%, 7 min) to obtain 34 mg of N-(3-(3-chlorophenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a gum, yield 10%.

EXAMPLE 79

N-(3-(m-tolyloxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0492] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 0.98 mmol) was dissolved in 10 ml anhydrous THF under nitrogen. m-cresol (130 mg, 130 μl, 1.18 mmol), triphenylphosphane (316 mg, 1.18 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (230 μl, 1.2 mmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. and then at RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient DCM/AcOEt 100/0 to 98/2) and reverse phase chromatography (column: Phenomenex Gemini-NX C18 75×30 mm 3 μm; mobile phase: [A: H.sub.2O (0.225% FA) B: MeCN]; gradient B %: 50%-80%, 7 min) to obtain 20 mg of N-(3-(m-tolyloxy)-2,3-dihydro-1H-inden-5-yl)acrylamide, as a white foam, yield 7%.

EXAMPLE 80

N-(3-(3-(methylthio)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0493] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 0.984 mmol) was dissolved in THF (10 ml) under N.sub.2. 3-(methylsulfanyl)phenol (174 mg, 1.24 mmol) and triphenylphosphane (316 mg, 1.2 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (240 μl, 1.18 mmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. and then at RT overnight. The solvent was evaporated and the crude product was purified by reverse phase chromatography (column: Phenomenex Gemini-NX C18 75×30 mm 3 μm; mobile phase: [A: H.sub.2O (0.225% FA) B: MeCN]; gradient B %: 50%-80%, 7 min) to obtain 24 mg of N-(3-(3-(methylthio)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a gum, yield 8%.

EXAMPLE 81

N-(3-(3-cyclopropylphenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0494] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (207 mg, 1.02 mmol) was dissolved in THF (10 ml) under nitrogen atmosphere. 3-cyclopropylphenol (172 mg, 1.22 mmol) and triphenylphosphane (327 mg, 1.22 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (0.24 ml, 1.2 mmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. and then at RT for 24 h. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient DCM/MeOH 100/0 to 97/3) and further via reverse phase chromatography (column: Phenomenex Gemini-NX C18 75×30 mm 3 μm; mobile phase: [A: H.sub.2O (0.225% FA) B: MeCN]; gradient B %: 50%-80%, 7 min) to obtain 9 mg of N-(3-(3-cyclopropylphenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a gum, yield 3%.

EXAMPLE 82

N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0495] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (200 mg, 0.984 μmol) was dissolved in THF (10 ml) under nitrogen atmosphere. 3-(trifluoromethyl)phenol (168 mg, 0.984 μmop and triphenylphosphane (316 mg, 1.18 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (0.24 ml, 1.2 mmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. and then at RT for 24 h. The solvent was evaporated and the crude product was purified by column chromatography (silica gel, gradient DCM/MeOH 100/0 to 98/2) to obtain 80 mg of N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 23%.

EXAMPLE 83

N-methyl-N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0496] To a solution of N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 288 μmol, see example 82) in 3 ml anhydrous DMF at 0° C. was added NaH (60% in mineral oil, 14 mg, 345 μmol). The temperature was allowed to rise to RT, the reaction mixture was stirred for 10 min at RT, then cooled again to 0° C. before adding slowly iodomethane (30 μl, 432 μmol). The reaction mixture was allowed to rise RT and stirred 3 h at RT. The reaction mixture was cooled to 0° C., ice cold water was added followed by an extraction with AcOEt. Then the combined organic layer was washed with water and an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 50 mg of N-methyl-N-(1-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a yellow gum, yield 48%.

EXAMPLES 84 AND 85

Enantiomers 1 and 2 of N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0497] Chiral separation of N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide (example 45) was realized as follows:

[0498] 300 mg of N-(2-((3-trifluorophenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide were dissolved in 50 ml of EtOH and purified by reverse chiral phase chromatography (column Chiralcel OD-I 20 μm, 350×76 mm, eluant heptane/EtOH 90/10, 400 ml/min). Fractions of each enantiomer were combined and evaporated, then lyophilized.

[0499] A first enantiomer, designated “Enantiomer 1”, was isolated as a white amorphous solid (132 mg, yield 44%) with 99.5% e.e.

[0500] A second enantiomer, designated “Enantiomer 2” was isolated as a white amorphous solid (126 mg, yield 42%) with 99.5% e.e.

EXAMPLES 86 AND 87

Enantiomers 1 and 2 of N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0501] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (600 mg, 2.95 mmol) was dissolved in THF (30 ml) under N.sub.2. 4-(trifluoromethyl)phenol (605 mg, 3.54 mmol) and triphenylphosphane (948 mg, 3.54 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (704 μl, 3.54 mmol) solubilized in DCM (5 ml) and stirred 20 min at 0° C. and then at RT for 4 h. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient DCM/AcOEt 100/0 to 98/2) to obtain 290 mg of a mixture of two isomers which were separated by chiral SFC chromatography (column IB-N5 30×250 mm, mobile phase A: CO2, B: MeOH (0.1% diethylamine), A/B 80/20) to obtain after lyophilization 120 mg of enantiomer 1 of N-(3-(4-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous white solid, 11% yield and 95 mg of enantiomer 2 of N-(3-(4-(trifluoro-methyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as an amorphous white solid, 9% yield.

EXAMPLE 88

N-[3-[[5-(trifluoromethyl)pyridin-2-yl]oxy]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0502] N-(3-hydroxy-2,3-dihydro-1H-inden-5-yl)acrylamide (202 mg, 1.00 mmol) was dissolved in THF (10 ml) under N.sub.2. 2-hydroxy-5-(trifluoromethyl)pyridine (201 mg, 1.20 mmol) and triphenylphosphane (313 mg, 1.20 mmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (235 μl, 1.20 mmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. then RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient DCM/AcOEt 100/0 to 97/3) to obtain 130 mg of N-[3-[[5-(trifluoromethyl)-pyridin-2-yl]oxy]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white solid, yield 38%.

EXAMPLE 89

N-methyl-N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)-acrylamide

[0503] To a solution of N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide (100 mg, 288 μmol, example 45) in 3 ml anhydrous DMF at 0° C. was added NaH (60% in mineral oil) (14 mg, 345 μmol). The temperature was allowed to rise to RT, stirred for 10 min at RT, then cooled down again to 0° C. before adding slowly iodomethane (30 μl, 432 μmol). The reaction mixture was allowed to rise RT and stirred 3 h at RT. The reaction mixture was cooled to 0° C., ice cold water was added followed by an extraction with AcOEt. Then the combined organic layer was washed with water and an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 70/30) to obtain 83 mg of N-methyl-N-(1-(3-(trifluoromethyl)phenoxy)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless gum, yield 80%.

EXAMPLE 90

N-[2-fluoro-3-[4-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0504] N-(2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (37 mg, 169 μmol, synthesis described in example 91) was dissolved in AcOEt (3 ml). 4-(trifluoromethyl)aniline (42 μl, 338 μmol) and TFA (38 μl, 506 μmol) were added. STAB (112 mg, 506 μmol) was added to the mixture in several portions. The reaction mixture was stirred for 6 h at 35° C. An aqueous solution of NaOH 1N was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 19 mg of N-[2-fluoro-3-[4-(trifluoromethyl)-anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide as a white solid, yield 31%.

EXAMPLE 91

N-(2-fluoro-3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0505] ##STR00019##

Step 1: Synthesis of 6-bromo-2-fluoro-2,3-dihydro-1H-inden-1-one

[0506] 6-bromo-indanone (2 g, 9.5 mmol) was dissolved in anhydrous MeOH (80 ml). Selectfluor (4 g, 11 mmol) was added. The reaction mixture was stirred for 7 h at 50° C. The solvent was evaporated at reduced pressure. DCM was added and insoluble material was filtered. The organic layer was washed with a saturated aqueous solution of NaHCO.sub.3, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/DCM 100/0 to 92/8) to obtain 220 mg of 6-bromo-2-fluoro-2,3-dihydro-1H-inden-1-one as a white solid, yield 10%.

Step 2: Synthesis of tert-butyl (2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)carbamate

[0507] A microwave tube equipped with a magnetic stirring bar was charged with 6-bromo-2-fluoro-2,3-dihydro-1H-inden-1-one (100 mg, 437 μmop, tert-butyl carbamate (63 mg, 524 μmol) and cesium carbonate (203 mg, 611 μmol). Anhydrous 1,4-dioxane (2 ml) was added and the mixture was charged with nitrogen gas. JohnPhos (14 mg, 44 μmol) and palladium (II) acetate (5 mg, 22 μmol) were added. Then the microwave tube was sealed and the reaction mixture was stirred for 2 h at 90° C. in a sand bath. The reaction mixture was poured into water after cooling down to RT and extracted with AcOEt several times. The combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient DCM/AcOEt 100/0 to 0/100) to obtain 50 mg of tert-butyl (2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)carbamate as a brown oil, yield 43%.

Step 3: Synthesis of 6-amino-2-fluoro-2,3-dihydro-1H-inden-1-one

[0508] A solution of tert-butyl (2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)carbamate (50 mg, 189 μmol) in DCM (3 ml) was cooled down to 0° C. before adding slowly TFA (365 μl, 4.71 mmol) and stirred at RT for 1 h. The reaction mixture was diluted with DCM. An aqueous solution of 1N NaOH was added, followed by extraction with DCM several times. The combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product, 6-amino-2-fluoro-2,3-dihydro-1H-inden-1-one was used for the next step without further purification.

Step 4: Synthesis of N-(2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide

[0509] 6-amino-2-fluoro-2,3-dihydro-1H-inden-1-one (31 mg, 188 μmol) was dissolved in THF (1.5 ml). Triethylamine (34 μl, 244 μmol) was added. The reaction mixture was cooled down to 0° C. before adding slowly acryloyl chloride (21 μl, 244 μmol) and stirred at RT for 1 h. The reaction mixture was diluted with AcOEt. A saturated aqueous solution of NaHCO.sub.3 was added, followed by extraction with AcOEt several times. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 75/25 to obtain 20 mg of N-(2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide as a white solid, yield 49%.

Step 5: Synthesis of N-(2-fluoro-3-((3-trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0510] N-(2-fluoro-3-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (20 mg, 91 μmol) was dissolved in AcOEt (1.5 ml). 3-trifluoromethylaniline (11 μl, 91 μmol) and TFA (21 μl, 274 μmol) were added. STAB (35 mg, 164 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 4 h at 40° C. An aqueous solution of 1N NaOH was added, followed by extraction with AcOEt several times. Then the combined organic layer was washed with brine, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 95/5 to 85/15) to obtain 9 mg of N-(2-fluoro-3-((3-trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a colorless oil, yield 27%.

EXAMPLE 92

N-[2-fluoro-3-[4-(trifluoromethyl)phenoxy]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0511] N-(2-fluoro-3-hydroxy-indan-5-yl)acrylamide (40 mg, 181 μmol) was dissolved in THF (3 ml) under N.sub.2. 4-(trifluoromethyl)phenol (37 mg, 217 μmol) and triphenyl-phosphane (60 mg, 217 μmol) were added. The reaction mixture was cooled down to 0° C. before adding slowly DIAD (45 μl, 217 μmol) solubilized in THF (5 ml) and stirred 20 min at 0° C. then RT overnight. The solvent was evaporated and the crude product was purified by column chromatography (SiO.sub.2, gradient cyclohexane/AcOEt, 100/0 to 50/50) to obtain 50 mg of N-[2-fluoro-3-[4-(trifluoromethyl)phenoxy]indan-5-yl]acrylamide as a mixture which was further purified by a second column chromatography (SiO.sub.2, gradient DCM/AcOEt, 100/0 to 90/10) to obtain 9 mg N-[2-fluoro-3-[4-(trifluoromethyl)-phenoxy]indan-5-yl]acrylamide as white solid, yield 13%.

EXAMPLE 93

N-methyl-N-(2-methyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0512] ##STR00020##

[0513] To a solution of N-(1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (700 mg, 3.48 mmol) in 17 ml anhydrous DMF at 0° C. was added NaH (60% in mineral oil) (167 mg, 4.17 mmol). The temperature was allowed to rise to RT, stirred for 10 min at RT, then cooled down again to 0° C. before adding slowly iodomethane (432 μl, 6.96 mmol). The reaction mixture was allowed to rise RT and stirred 3 h at RT, adding 32 μl of iodomethane and stirred 2 h at RT. The reaction mixture was cooled to 0° C., ice cold water was added followed by an extraction with AcOEt. Then the combined organic layer was washed with water and an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 100/0 to 50/50) to obtain 110 mg of N-methyl-N-(2-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide as gum, yield 15%.

[0514] N-methyl-N-(2-methyl-1-oxo-2,3-dihydro-1H-inden-5-yl)acrylamide (45 mg, 196 μmop was dissolved in AcOEt (1 ml). 3-(trifluoromethyl)aniline (29 μl, 236 μmol) and TFA (30 μl, 393 μmol) were added. STAB (50 mg, 236 μmol) was added to the mixture in one portion. The reaction mixture was stirred for 3 h at 35° C. An aqueous solution of NaOH 1N (20 ml) was added, followed by an extraction with AcOEt. Then the combined organic layer was washed with an aqueous saturated solution of NaCl, dried over Na.sub.2SO.sub.4, filtered and concentrated at reduced pressure. The crude product was purified by column chromatography (silica gel, gradient cyclohexane/AcOEt 90/10 to 40/60) to obtain 6 mg N-methyl-N-(2-methyl-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide as a gum, yield 8%.

EXAMPLE 94

N-[(cis)-3-methoxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0515] ##STR00021## ##STR00022##

Step 1: Trimethyl-[(6-nitro-3H-inden-1-yl)oxy]silane

[0516] To a solution of 6-nitroindan-1-one (3 g, 16.9 mmol, 1 eq) and TEA (3.43 g, 33.9 mmol, 4.71 ml, 2 eq) in DCM (60 ml) was added trimethylsilyl trifluoromethanesulfonate (5.65 g, 25.4 mmol, 4.59 ml, 1.5 eq) at 0° C. and the mixture was stirred at 0° C. for 0.5 h. The reaction mixture was concentrated under vacuum at 30° C. to obtain a residue which was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt gradient 200/1 to 10/1) to obtain trimethyl-[(6-nitro-3H-inden-1-yl)oxy]silane (1.4 g, 5.61 mmol, 33% yield) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.19 (d, J=2.0 Hz, 1H, Ar), 8.13 (dd, J=2.0, 8.0 Hz, 1H, Ar), 7.50 (d, J=8.0 Hz, 1H, Ar), 5.59 (t, J=2.4 Hz, 1H, CH), 3.39 (d, J=2.4 Hz, 2H, CH.sub.2), 0.35 (s, 9H, CH.sub.3).

Step 2: 6-nitroinden-1-one

[0517] To a mixture of Pd(OAc).sub.2 (3.69 g, 16.44 mmol, 1 eq) in MeCN (80 ml) was added a solution of trimethyl-[(6-nitro-3H-inden-1-yl)oxy]silane (4.1 g, 16.44 mmol, 1 eq) in DCM (40 ml) under N.sub.2. The reaction bottle was aluminum foil-wrapped. The mixture was stirred at 20° C. for 4 hr. TLC indicated the reaction was completed. The reaction mixture was filtered and the filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=100/1 to 5/1) to obtain 6-nitroinden-1-one (2.2 g, 10.68 mmol, 64.93% yield, 85% purity) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.34 (dd, J=2.0, 7.9 Hz, 1H, Ar), 8.26 (s, 1H, Ar), 7.73 (d, J=6.0 Hz, 1H, CHCH), 7.30 (d, J=7.9 Hz, Ar), 6.24 (d, J=6.0 Hz, 1H, CHCH).

Step 3: 6-Nitro-3-[3-(trifluoromethyl)anilino]indan-1-one

[0518] A mixture of 6-nitroinden-1-one (2.2 g, 12.56 mmol, 1 eq) and 3-(trifluoromethyl)aniline (4.05 g, 25.12 mmol, 3.14 ml, 2 eq) in THF (7 ml) was stirred at 20° C. for 12 hr. TLC indicated the reaction was completed. The reaction mixture was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=100/1 to 5/1) to obtain 6-nitro-3-[3-(trifluoromethyl)anilino]indan-1-one (2.4 g, 6.28 mmol, 50.00% yield, 88% purity) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.62 (d, J=2.0 Hz, 1H, Ar), 8.54 (dd, J=2.0, 8.4 Hz, 1H, Ar), 7.91 (d, J=8.4 Hz, 1H, Ar), 7.37 (t, J=8.0 Hz, 1H, Ar), 7.10 (d, J=7.6 Hz, 1H, Ar), 6.95 (s, 1H, ArH), 6.87 (d, J=8.0 Hz, 1H, Ar), 5.36 (dt, J=3.6, 8.0 Hz, 1H, CH), 4.26 (d, J=8.8 Hz, 1H, ArNH), 3.41 (dd, J=7.2, 19.2 Hz, 1H, CH.sub.2), 2.71 (dd, J=3.6, 19.2 Hz, 1H, CH.sub.2). ES-MS m/z 337.3 [M+H]

Step 4: 6-Nitro-3-[3-(trifluoromethyl)anilino]indan-1-ol

[0519] To a solution of 6-nitro-3-[3-(trifluoromethyl)anilino]indan-1-one (1 g, 2.97 mmol, 1 eq) in MeOH (15 ml) was added NaBH.sub.4 (225 mg, 5.95 mmol, 2 eq) in portions at 0° C. The mixture was stirred at 20° C. for 2 hr. TLC indicated the reaction was completed. The reaction mixture was quenched by addition 1N HCl (10 ml) at 0° C., then diluted with water (15 ml) and extracted with EtOAc (30 ml*2), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=100/1 to 3/1) to obtain 6-nitro-3-[3-(trifluoromethyl)anilino]-indan-1-ol (990 mg, 2.49 mmol, 83.65% yield, 85% purity) as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.33 (d, J=1.6 Hz, 1H, Ar), 8.18 (dd, J=2.0, 8.4 Hz, 1H, Ar), 7.53 (d, J=8.6 Hz, 1H, Ar), 7.34 (t, J=8.0 Hz, 1H, Ar), 7.06 (br d, J=8.0 Hz, 1H, Ar), 6.98 (s, 1H, Ar), 6.93-6.87 (m, 1H, Ar), 5.29 (t, J=6.8 Hz, 1H, CH), 4.99 (t, J=7.2 Hz, 1H, CH), 3.18 (td, J=6.8, 13.2 Hz, 1H, CH.sub.2), 1.99-1.87 (m, 1H, CH.sub.2). ES-MS m/z 339.3 [M+H].sup.+, Retention time: 2.347 min.

Step 5: 3-Methoxy-5-nitro-N-[3-(trifluoromethyl)phenyl]indan-1-amine

[0520] A mixture of 6-nitro-3-[3-(trifluoromethyl)anilino]indan-1-ol (990 mg, 2.93 mmol, 1 eq), MeI (830.78 mg, 5.85 mmol, 364.38 μl, 2 eq) and Ag.sub.2O (3.39 g, 14.63 mmol, 5 eq) in DCM (10 ml) was stirred at 20° C. for 12 hr. TLC indicated the reaction was completed. The reaction mixture was filtered and the filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=100/1 to 5/1) to obtain 3-methoxy-5-nitro-N-[3-(trifluoromethyl)phenyl]indan-1-amine (690 mg, 1.84 mmol, 62.91% yield, 94% purity) was obtained as a yellow solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.32 (d, J=2.0 Hz, 1H, Ar), 8.20 (dd, J=2.0, 8.4 Hz, 1H, Ar), 7.56 (d, J=8.4 Hz, 1H, Ar), 7.33 (t, J=8.0 Hz, 1H, Ar), 7.05 (d, J=7.6 Hz, 1H, Ar), 6.98 (s, 1H, Ar), 6.90 (br d, J=8.0 Hz, 1H, Ar), 5.02 (t, J=6.8 Hz, 1H, CH), 4.82 (t, J=6.0 Hz, 1H, CH), 3.52 (s, 3H, CH.sub.3), 3.04 (td, J=6.8, 13.4 Hz, 1H, CH.sub.2), 2.05-1.97 (m, 1H, CH.sub.2). ES-MS m/z 353.4 [M+H].sup.+, Retention time: 1.014 min.

Step 6: 3-methoxy-N1-[3-(trifluoromethyl)phenyl]indane-1,5-diamine

[0521] To a solution of 3-methoxy-5-nitro-N-[3-(trifluoromethyl)phenyl]indan-1-amine (690 mg, 1.96 mmol, 1 eq) in AcOEt (6 ml) was added Lindlar catalyst (600 mg) under N.sub.2 atmosphere. The suspension was degassed and purged with H.sub.2 for 3 times. The mixture was stirred under H.sub.2 (15 Psi) at 20° C. for 4 hr. TLC indicated the reaction was completed. The reaction mixture was filtered and the filtrate was concentrated under vacuum to obtain a residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=100/1 to 3/1) to obtain 3-methoxy-N1-[3-(trifluoromethyl)phenyl]indane-1,5-diamine (350 mg, 977.28 μmol, 49.90% yield, 90% purity) as a yellow solid. .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ=7.27 (t, J=7.6 Hz, 1H, Ar), 6.96 (s, 1H, ArNH), 6.94 (br d, J=8.0 Hz, 2H, Ar), 6.80 (d, J=7.6 Hz, 1H, Ar), 6.59 (d, J=2.0 Hz, 1H, Ar), 6.52 (dd, J=2.0, 8.0 Hz, 1H, Ar), 6.35 (d, J=8.4 Hz, 1H, Ar), 5.06 (s, 2H, ArNH.sub.2), 4.73 (q, J=7.2 Hz, 1H, CH), 4.64 (t, J=6.8 Hz, 1H, CH), 3.34-3.33 (m, 3H, CH.sub.3), 2.94-2.87 (m, 1H, CH.sub.2), 1.64-1.46 (m, 1H, CH.sub.2).

Step 7: N-[(cis)-3-methoxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0522] To a solution of 3-methoxy-N1-[3-(trifluoromethyl)phenyl]indane-1,5-diamine (400 mg, 1.24 mmol, 1 eq) in DCM (4 ml) was a solution of acryloyl chloride (124 mg, 1.37 mmol, 111.31 μl, 1.1 eq) in DCM (1.5 ml) at 0° C. Then the mixture was stirred at 0° C. for 0.5 h. LCMS showed the reaction was completed. The reaction mixture was poured into H.sub.2O (10 ml) and extracted with EA (3×10 ml). The combined organic layer was washed with brine (20 ml), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain a residue. The residue was purified by prep-HPLC (column: Phenomenex Gemini-NX C18 75*30 mm*3 um; mobile phase: [water (0.225% FA)-MeON]; B %: 45%-75%, 7 min) to obtain N-[(cis)-3-methoxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide (235 mg, 623.76 μmol, 50.26% yield, 99.9% purity) as a yellow solid. .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ=10.19 (s, 1H, CONH), 7.84 (s, 1H, Ar), 7.52 (dd, J=1.6, 8.4 Hz, 1H, Ar), 7.33-7.27 (m, 1H, Ar), 7.23 (d, J=8.0 Hz, 1H, Ar), 7.00 (s, 1H, ArNH), 7.00-6.95 (m, 1H, Ar), 6.84 (d, J=7.6 Hz, 1H, Ar), 6.51 (d, J=8.4 Hz, 1H, Ar), 6.48-6.38 (m, 1H, CH.sub.2CH), 6.31-6.21 (m, 1H, CHCH.sub.2), 5.75 (dd, J=2.0, 10.0 Hz, 1H, CHCH.sub.2), 4.89 (q, J=7.6 Hz, 1H, CH), 4.77 (t, J=6.8 Hz, 1H, CH), 3.39 (s, 3H, CH.sub.3), 3.01 (td, J=6.8, 12.4 Hz, 1H, CH.sub.2), 1.63 (td, J=7.6, 12.4 Hz, 1H, CH.sub.2).

EXAMPLE 95

N-[(trans)-2-hydroxy-1-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0523] ##STR00023##

Step 1: 5-Nitro-2,3-dihydro-1H-inden-2-ol

[0524] To a solution of 5-nitroindan-2-one (13 g, 73.38 mmol, 1 eq) in MeOH (550 ml) was added in portions NaBH.sub.4 (5.55 g, 146.76 mmol, 2 eq) at 0° C. The mixture was stirred at 0° C. for 1 h. TLC showed the reaction was completed. The mixture was poured into ice-cooled HCl solution (100 ml, 1 M). The aqueous phase was extracted with AcOEt (500 ml×3), dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain 5-nitroindan-2-ol (7.4 g, 41.32 mmol, 56.27% yield) as a black solid. .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.07-8.04 (m, 2H, Ar), 7.36 (d, J=8.4 Hz, 1H, Ar), 4.82-4.78 (m, 1H, CH), 3.46 (s, 1H, OH), 3.31-3.23 (m, 2H, CH.sub.2), 3.03-2.98 (m, 2H, CH.sub.2)

Step 2: 5-Nitro-1H-indene; 6-Nitro-1H-indene

[0525] A mixture of 5-nitroindan-2-ol (2 g, 11.16 mmol, 1 eq) and H.sub.2SO.sub.4 (9 M, 80.00 ml, 64.50 eq) was stirred at 130° C. for 2 h. TLC showed the starting material remained and two new spots were detected. The mixture was extracted with AcOEt (50 ml×3). The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain the residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=1/0 to 50/1) to obtain a mixture of 5-nitro-1H-indene and 6-nitro-1H-indene (750 mg, 4.65 mmol, 41.69% yield) as a white solid.

Step 3: (1aR,6aS)-4-nitro-6,6a-dihydro-1aH-indeno[1,2-b]oxirene and (1aS,6aR)-3-nitro-6,6a-dihydro-1aH-indeno[1,2-b]oxirene

[0526] To a solution of 5-nitro-1H-indene and 6-nitro-1H-indene (1.80 g, 11.17 mmol, 1 eq) in DCM (40 ml) was added m-CPBA (4.82 g, 22.34 mmol, 80% purity, 2 eq). The mixture was stirred at 25° C. for 16 h. TLC showed the reaction was completed. The mixture was diluted with DCM (150 ml) and washed with saturated Na.sub.2SO.sub.3 solution (3×50 ml) and washed with saturated NaHCO.sub.3 solution (80 ml). The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain a mixture cis-4-nitro-6,6a-dihydro-1aH-indeno[1,2-b]oxirene and cis-3-nitro-6,6a-dihydro-1 aH-indeno[1,2-b]oxirene (2 g, 10.73 mmol, 96% yield, 95% purity) as a yellow oil.

[0527] .sup.1H NMR (400 MHz, CDCl.sub.3) δ=8.36 (d, J=2.0 Hz, 1H, Ar), 8.18 (dd, J=2.0, 8.0 Hz, 1H, Ar), 8.13-8.11 (m, 2H, Ar), 7.65 (d, J=8.0 Hz, 1H, Ar), 7.39 (d, J=8.0 Hz, 1H, Ar), 4.37-4.33 (m, 2H, CHCH), 4.26-4.22 (m, 2H, CHCH), 3.33 (d, J=18.4 Hz, 2H, CH.sub.2), 3.12-3.05 (m, 2H, CH.sub.2).

Step 4: Trans-5-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol and Trans-6-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol

[0528] ##STR00024##

[0529] To a solution of 3-(trifluoromethyl)aniline (1.48 g, 9.19 mmol, 1.15 ml, 1 eq) in pentan-1-ol (80 ml) was added cis-4-nitro-6,6a-dihydro-1aH-indeno[1,2-b]oxirene and cis-3-nitro-6,6a-dihydro-1aH-indeno[1,2-b]oxirene (1.98 g, 11.18 mmol, 1.22 eq). The mixture was stirred at 140° C. for 6 h. LCMS showed the reaction was completed. The mixture was concentrated under reduced pressure to obtain the residue. The residue was purified by column chromatography (SiO.sub.2, Petroleum ether/AcOEt=1/0 to 9/1) to obtain trans-5-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (990 mg, 2.93 mmol, 31.85% yield) as a yellow solid and trans-6-nitro-1-((3-(trifluoro-methyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (540 mg, 1.60 mmol, 17.37% yield) as a yellow solid.

[0530] Trans-5-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol. .sup.1HNMR (400 MHz, DMSO-d.sub.6) δ=8.12-8.08 (m, 2H, Ar), 7.49-7.44 (m, 1H, Ar), 7.32 (t, J=8.0 Hz, 1H, Ar), 7.04-7.02 (m, 2H, Ar), 6.87 (d, J=7.6 Hz, 1H, Ar), 6.58 (d, J=8.4 Hz, 1H, NH), 5.55 (d, J=5.2 Hz, 1H, OH), 4.82-4.79 (m, 1H, CH), 4.31-4.27 (m, 1H, CH), 3.27 (d, J=6.8 Hz, 1H, CH.sub.2), 2.85 (dd, J=6.0, 16.0 Hz, 1H, CH.sub.2)

[0531] Trans-6-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol. .sup.1HNMR (400 MHz, DMSO-d.sub.6) δ=8.16 (dd, J=2.0, 8.0 Hz, 1H), 8.04 (d, J=1.6 Hz, 1H, Ar), 7.55 (d, J=8.4 Hz, 1H, Ar), 7.33 (t, J=7.6 Hz, 1H, Ar), 7.07-7.05 (m, 2H, Ar), 6.88 (d, J=8.0 Hz, 1H, Ar), 6.56 (d, J=8.0 Hz, 1H, NH), 5.56 (d, J=4.8 Hz, 1H, OH), 4.83-4.80 (m, 1H, CH), 4.31-4.25 (m, 1H, CH), 3.28 (d, J=6.4 Hz, 1H, CH.sub.2), 2.86 (dd, J=5.6, 16.8 Hz, 1H, CH.sub.2)

Step 5: Trans-5-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol

[0532] To a solution of trans-5-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-11H-inden-2-ol (370.00 mg, 1.09 mmol, 1 eq) in MeOH (10 ml) was added Pd/C (37 mg, 10%/C) and Et.sub.3N (72.70 mg, 718.46 μmol, 0.1 ml, 0.66 eq). The mixture was degassed with H.sub.2 (15 psi) and stirred at 25° C. under H.sub.2 (15 psi) for 30 mins. TLC showed trace starting material remained and one new spot was detected. The mixture was filtered and concentrated under reduced pressure to obtain trans-5-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (370 mg, crude) as a yellow oil.

[0533] .sup.1H NMR (400 MHz, DMSO-d6) δ=7.26 (t, J=8.0 Hz, 1H, Ar), 7.00-6.97 (m, 2H, Ar), 6.87 (d, J=7.6 Hz, 1H, Ar), 6.79 (d, J=7.6 Hz, 1H, Ar), 6.42-6.38 (m, 2H, Ar), 6.23 (d, J=7.6 Hz, 1H, NH), 5.20 (d, J=4.8 Hz, 1H, OH), 4.99 (s, 2H, NH.sub.2), 4.46-4.42 (m, 1H, CH), 4.10-4.08 (m, 1H, CH), 3.03 (dd, J=6.4, 16.0 Hz, 1H, CH.sub.2), 2.59 (d, J=4.8 Hz, 1H, CH.sub.2).

Step 6: Trans-N-(2-hydroxy-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0534] To a solution of trans-5-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-al (280 mg, 908.2 μmol, 1 eq) and DIEA (234.76 mg, 1.82 mmol, 316.39 μl, 2 eq) in DCM (6 ml) were added a solution of acryloyl chloride (82.20 mg, 908.21 μmol, 74.05 μl, 1 eq) in DCM (0.5 ml) at 0° C. The mixture was stirred at 25° C. for 1 h. LCMS showed the reaction was completed. The mixture was diluted with DCM (10 ml) and washed with water (5 ml). The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain the residue, which was purified by prep-HPLC (column: Unisil 3-100 C18 ultra 150*50 mm*3 um; mobile phase: [water (0.225% FA)-MeCN]; B %: 40%-60%, 10 min) to obtain trans-N-(2-hydroxy-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)-acrylamide (116.6 mg, 321.9 μmol, 35.44% yield, 100% purity) as an off-white solid.

[0535] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ=10.11 (s, 1H, CONH), 7.64 (s, 1H, Ar), 7.40 (dd, J=1.6, 8.4 Hz, 1H, Ar), 7.29 (t, J=8.0 Hz, 1H, Ar), 7.18 (d, J=8.0 Hz, 1H, Ar), 7.02-7.00 (m, 2H, Ar), 6.82 (d, J=7.6 Hz, 1H, Ar), 6.47-6.38 (m, 2H, CHCH.sub.2, NH), 6.27-6.22 (m, 1H, CHCH.sub.2), 5.74 (dd, J=2.0, 10.0 Hz, 1H, CHCH.sub.2), 5.34 (d, J=4.8 Hz, 1H, OH), 4.62-5.91 (m, 1H, CH), 4.21-4.16 (m, 1H, CH), 3.17 (dd, J=6.8, 16.4 Hz, 1H, CH.sub.2), 2.72 (dd, J=5.6, 16.0 Hz, 1H, CH.sub.2).

EXAMPLE 96

N-[rac-(2R,3R)-2-hydroxy-3-[3-(trifluoromethyl)anilino]-2,3-dihydro-1H-inden-5-yl]acrylamide

[0536] ##STR00025##

[0537] Step 1: Trans-6-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol

[0538] To a solution of trans-6-nitro-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (300.00 mg, 886.84 μmol, 1 eq) in MeOH (10 ml) was added Pd/C (30 mg, 10% purity). The mixture was degassed with H.sub.2 (15 psi) and stirred at 25° C. under H.sub.2 (15 psi) for 4 h. LCMS showed the reaction was completed. The mixture was filtered and concentrated under reduced pressure to obtain trans-6-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (200 mg, 648.72 μmol, 73.15% yield) as a yellow solid.

[0539] .sup.1H NMR (400 MHz, DMSO-d.sub.6) δ=7.27 (t, J=8.0 Hz, 1H, Ar), 7.01-6.97 (m, 2H, Ar), 6.86-6.78 (m, 2H, Ar), 6.45-6.39 (m, 3H, Ar, NH), 5.22 (d, J=5.6 Hz, 1H, OH), 4.89 (s, 2H, NH.sub.2), 4.54-4.51 (m, 1H, CH), 4.15-4.09 (m, 1H, CH), 2.98 (dd, J=6.8, 15.2 Hz, 1H, CH.sub.2), 2.59-2.54 (m, 1H, CH.sub.2).

Step 2: Trans-N-(2-hydroxy-3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide

[0540] To a solution of trans-6-amino-1-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-2-ol (170 mg, 551.42 μmol, 1 eq) and DIPEA (142.53 mg, 1.10 mmol, 192.09 μl, 2 eq) in DCM (10 ml) were added a solution of acryloyl chloride (69.9 mg, 772 μmol, 63 μl, 1.4 eq) in DCM (0.5 ml) at 0° C. The mixture was stirred at 25° C. for 1 h. LCMS showed the reaction was completed. The mixture was diluted with DCM (10 ml) and washed with water (5 ml). The organic phase was dried over Na.sub.2SO.sub.4, filtered and concentrated under reduced pressure to obtain the residue. The residue was purified by prep-TLC (Petroleum ether/AcOEt=1/1) and prep-HPLC (column: Unisil 3-100 C18 ultra 150*50 mm*3 um; mobile phase: [water (0.225% FA)-MeCN]; B %: 38%-58%, 10 min) to obtain trans-N-(2-hydroxy-3-((3-(trifluoromethyl)phenyl)amino)-2,3-dihydro-1H-inden-5-yl)acrylamide (89.7 mg, 248 μmol, 45% yield, 100% purity) as a white solid.

[0541] .sup.1H NMR (400 MHz, DMSO-d6) δ=10.07 (s, 1H, CONH), 7.60 (dd, J=1.2, 8.0 Hz, 1H, Ar), 7.50 (s, 1H, Ar), 7.30 (t, J=8.0 Hz, 1H, Ar), 7.18 (d, J=8.4 Hz, 1H, Ar), 7.02-7.00 (m, 2H, Ar), 6.83 (d, J=7.6 Hz, 1H, Ar), 6.49 (d, J=8.0 Hz, 1H, NH), 6.39 (dd, J=10.0, 17.2 Hz, 1H, CHCH.sub.2), 6.21 (dd, J=1.6, 16.8 Hz, 1H, CHCH.sub.2), 5.71 (dd, J=2.0, 10.0 Hz, 1H, CHCH.sub.2), 5.36 (d, J=5.2 Hz, 1H, OH), 4.68-4.65 (m, 1H, CH), 4.22-4.18 (m, 1H, CH), 3.11 (dd, J=6.8, 15.6 Hz, 1H, CH.sub.2), 2.69 (dd, J=6.0, 15.6 Hz, 1H, CH.sub.2).

[0542] The table herein below illustrates the chemical structures and physical properties of a number of compounds of formula (I).

[0543] In the table: [0544] the proton magnetic resonance spectra (.sup.1H NMR), as described below, are recorded at 400 MHz in DMSO-d.sub.6, using the DMSO-d.sub.6 peak as reference. The chemical shifts δ are expressed in parts per million (ppm). The signals observed are expressed as follows: s=singlet; d=doublet; t=triplet; m=multiplet or br s=broad singlet; br m=broad multiplet [0545] the LCMS characteristics, as described below, successively indicated the high-performance liquid chromatography analytical method used and detailed below (A and B), the [M+H].sup.+ or [M−H].sup.− peak identified by mass spectrometry and the retention time (Tr) of the compound, expressed in minutes.

[0546] Method A

[0547] Column: Acquity UPLC/SQD CORTECS C18+2.1×50 mm 1.6 μm (Waters)

[0548] Gradient: MeCN/H.sub.2O with 0.1%. FA from 2 to 100% during 3 min, 1 ml/min

[0549] Method B

[0550] Column: Acquity UPLC/SQD CORTECS C18+2.1×50 mm 1.6 μm (Waters)

[0551] Gradient: MeCN/H.sub.2O with 0.1%. FA from 2 to 100% during 10 min, 1 ml/min

[0552] Method C

[0553] Column: Kinetex EVO C18 2.1×30 mm, 5 μm

[0554] Gradient: 0.0 min 5% B.fwdarw.0.8 min 95% B.fwdarw.1.2 min 95% B.fwdarw.1.21 min 5% B.fwdarw.1.55 min 5% B, 1.5 ml/min, mobile phase: A: 0.0375% TFA in water (v/v), B: 0.01875% TFA in Acetonitrile (v/v)

[0555] Method D

[0556] Column: Acquity UPLC/SQD CSH C18 2.1×50 mm 1.7 μm (Waters)

[0557] Gradient: MeCN/H.sub.2O with 0.1% FA from 5 to 100% during 2.5 min, 1 ml/min

[0558] Compounds of formula (I) underwent biochemical studies in order to determine their capacity to inhibit YAP1/TAZ-TEAD or TEAD-dependent gene transcription.

TABLE-US-00001 Obs Obs Example Ion(s) Ion(s) Tr Analytical No IUPAC name NMR Description type mass (min) method 1 N-(1-((3-(trifluoro-methyl)phenyl)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.72- [M − H]− 344 1.43 A amino)-2,3-dihydro-1H-inden-5-yl)- 1.88 (m, 1 H) 2.41-2.46 (m, 1 H) 2.77- acrylamide 2.88 (m, 1 H) 2.89-3.01 (m, 1 H) 4.99 (q, J = 7.03 Hz, 1 H) 5.73 (dd, J = 9.99, 2.03 Hz, 1 H) 6.24 (dd, J = 16.95, 2.03 Hz, 1 H) 6.34- 6.50 (m, 2 H) 6.82 (d, J = 7.53 Hz, 1 H) 6.94- 7.03 (m, 2 H) 7.21 (d, J = 8.28 Hz, 1 H) 7.29 (t, J = 8.16 Hz, 1 H) 7.40 (dd, J = 8.28, 1.64 Hz, 1 H) 7.67 (s, 1 H) 10.09 (s, 1 H) 2 N-(1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.78 [M − H]− 344 1.85 A (trifluoro-methyl)phenyl)-amino)- (m, 1 H) 2.52 (m partially hidden, 1 H) 2.82 2,3-dihydro-1H-inden-5-yl)-acrylamide (m, 1 H) 2.95 (m, 1 H) 4.99 (m, 1 H) 5.74 Enantiomer 1 (dd, J = 2.1 et 10.1 Hz, 1 H) 6.24 (dd, J = 2.1 et 17.1 Hz, 1 H) 6.41 (d, partially hidden, 1 H) 6.43 (dd, J = 10.1 et 17.1 Hz, 1 H) 6.82 (d, J = 8.1 Hz, 1 H) 6.97 (m, 2 H) 7.21 (d, J = 8.1 Hz, 1 H) 7.29 (t, J = 8.1 Hz, 1 H) 7.40 (dd, J = 2.1 et 8.1 Hz, 1 H) 7.68 (d, J = 2.1 Hz, 1 H) 10.10 (s, 1 H) 3 N-(1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm: 1.78 [M − H]− 344 1.85 A (trifluoromethyl)-phenyl)amino)- (m, 1 H) 2.52 (m partially hidden, 1 H) 2.82 2,3-dihydro-1H-inden-5-yl)-acrylamide (m, 1 H) 2.95 (m, 1 H) 4.99 (m, 1 H) 5.74 Enantiomer 2 (dd, J = 2.1 et 10.1 Hz, 1 H) 6.24 (dd, J = 2.1 et 17.1 Hz, 1 H) 6.41 (d, partially hidden, 1 H) 6.43 (dd, J = 10.1 et 17.1 Hz, 1 H) 6.82 (d, J = 8.1 Hz, 1 H) 6.97 (m, 2 H) 7.21 (d, J = 8.1 Hz, 1 H) 7.29 (t, J = 8.1 Hz, 1 H) 7.40 (dd, J = 2.1 et 8.1 Hz, 1 H) 7.68 (d, J = 2.1 Hz, 1 H) 10.10 (s, 1 H) 4 N-methyl-N-(1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.76- [M + H]+ 361 4.74 B (trifluoro-methyl)phenyl)-amino)- 1.90 (m, 1 H) 2.53-2.61 (m, 1 H) 2.80- 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.92 (m, 1 H) 2.93-3.04 (m, 1 H) 3.23 (s, 3 H) 5.07 (q, J = 7.53 Hz, 1 H) 5.53-5.62 (m, 1 H) 6.00-6.21 (m, 2 H) 6.48 (d, J = 8.28 Hz, 1 H) 6.84 (d, J = 7.53 Hz, 1 H) 6.96-7.04 (m, 2 H) 7.08 (dd, J = 7.78, 2.01 Hz, 1 H) 7.20 (s, 1 H) 7.28-7.35 (m, 2 H) 5 N-(1-((4-fluoro-phenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.70- [M − H]− 295 1.46 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.84 (m, 1 H) 2.41-2.46 (m, 1 H) 2.74- 2.85 (m, 1 H) 2.88-3.00 (m, 1 H) 4.87 (q, J = 7.19 Hz, 1 H) 5.69-5.79 (m, 2 H) 6.24 (dd, J = 16.89, 2.00 Hz, 1 H) 6.43 (dd, J = 16.89, 10.23 Hz, 1 H) 6.65-6.74 (m, 2 H) 6.88-6.97 (m, 2 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.39 (dd, J = 8.03, 1.51 Hz, 1 H) 7.65 (s, 1 H) 10.06 (s, 1 H) 6 N-(1-((4-fluoro-phenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm: 1.76 [M − H]− 294 1.46 A 2,3-dihydro-1H-inden-5-yl)-acrylamide (m, 1 H) 2.46 (m, 1 H) 2.80 (m, 1 H) 2.93 Enantiomer 1 (m, 1 H) 4.87 (m, 1 H) 5.73 (dd, J = 2.1 et 10.1 Hz, 1 H) 5.77 (d, J = 8.5 Hz, 1 H) 6.24 (dd, J = 2.1 et 17.0 Hz, 1 H) 6.43 (dd, J = 10.1 et 17.0 Hz, 1 H) 6.69 (dd, J = 4.6 et 9.1 Hz, 2 H) 6.92 (t, J = 9.1 Hz, 2 H) 7.21 (d, J = 8.1 Hz, 1 H) 7.39 (dd, J = 2.1 et 8.1 Hz, 1 H) 7.66 (d, J = 2.1 Hz, 1 H) 10.08 (s, 1 H) 7 N-(1-((4-fluoro-phenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm: 1.76 [M − H]− 294 1.45 A 2,3-dihydro-1H-inden-5-yl)-acrylamide (m, 1 H) 2.46 (m, 1 H) 2.80 (m, 1 H) 2.93 Enantiomer 2 (m, 1 H) 4.87 (m, 1 H) 5.73 (dd, J = 2.1 et 10.1 Hz, 1 H) 5.77 (d, J = 8.5 Hz, 1 H) 6.24 (dd, J = 2.1 et 17.0 Hz, 1 H) 6.43 (dd, J = 10.1 et 17.0 Hz, 1 H) 6.69 (dd, J = 4.6 et 9.1 Hz, 2 H) 6.92 (t, J = 9.1 Hz, 2 H) 7.21 (d, J = 8.1 Hz, 1 H) 7.39 (dd, J = 2.1 et 8.1 Hz, 1 H) 7.66 (d, J = 2.1 Hz, 1 H) 10.08 (s, 1 H) 8 N-(1-((3-fluoro-phenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.71- [M − H]− 295 1.27 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.88 (m, 1 H) 2.43-2.50 (m, 1 H) 2.75- 2.88 (m, 1 H) 2.89-3.02 (m, 1 H) 4.92 (q, J = 7.28 Hz, 1 H) 5.73 (dd, J = 10.04, 2.01 Hz, 1 H) 6.16-6.34 (m, 3 H) 6.38-6.61 (m, 3 H) 7.03-7.13 (m, 1 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.40 (dd, J = 8.03, 1.38 Hz, 1 H) 7.66 (s, 1 H) 10.07 (s, 1 H) 9 N-(1-((3,5-difluorophenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.70- [M − H]− 313 4.94 B 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.84 (m, 1 H) 2.52-2.57 (m, 1 H) 2.74- 2.87 (m, 1 H) 2.89-3.00 (m, 1 H) 4.93 (q, J = 7.28 Hz, 1 H) 5.74 (dd, J = 10.16, 2.13 Hz, 1 H) 6.16-6.28 (m, 2 H) 6.31-6.50 (m, 3 H) 6.57 (d, J = 8.03 Hz, 1 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.41 (dd, J = 8.03, 1.51 Hz, 1 H) 7.67 (s, 1 H) 10.08 (s, 1 H) 10 N-(1-((4-(trifluoromethyl)-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.74- [M − H]− 345 1.43 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.90 (m, 1 H) 2.52-2.56 (m, 1 H) 2.76- 2.88 (m, 1 H) 2.90-3.02 (m, 1 H) 5.00 (q, J = 7.28 Hz, 1 H) 5.73 (dd, J = 10.06, 2.03 Hz, 1 H) 6.24 (dd, J = 16.94, 2.03 Hz, 1 H) 6.43 (dd, J = 16.94, 10.06 Hz, 1 H) 6.64 (d, J = 8.03 Hz, 1 H) 6.82 (d, J = 8.53 Hz, 2 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.39 (br d, J = 8.53 Hz, 3 H) 7.68 (s, 1 H) 10.08 (s, 1 H) 11 N-(3-((3-(trifluoromethyl)-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.70- [M + H]+ 347 1.43 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.88 (m, 1 H) 2.53-2.58 (m, 1 H) 2.72- 2.96 (m, 2 H) 5.03 (q, J = 7.61 Hz, 1 H) 5.70 (dd, J = 10.10, 2.08 Hz, 1 H) 6.21 (dd, J = 16.90, 2.08 Hz, 1 H) 6.34-6.55 (m, 2 H) 6.82 (d, J = 7.53 Hz, 1 H) 6.93-7.04 (m, 2 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.30 (t, J = 8.28 Hz, 1 H) 7.53-7.64 (m, 2 H) 10.05 (s, 1 H) 12 N-(3-((4-(trifluoromethyl)-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.74- [M − H]− 345 1.48 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.88 (m, 1 H) 2.52-2.58 (m, 1 H) 2.74- 2.84 (m, 1 H) 2.86-2.98 (m, 1 H) 5.04 (q, J = 7.70 Hz, 1 H) 5.70 (dd, J = 10.16, 2.13 Hz, 1 H) 6.21 (dd, J = 16.88, 2.130, 1 H) 6.40 (dd, J = 16.88, 10.16 Hz, 1 H) 6.72 (d, J = 8.53 Hz, 1 H) 6.83 (d, J = 8.78 Hz, 2 H) 7.22 (d, J = 8.28 Hz, 1 H) 7.39 (d, J = 8.78 Hz, 2 H) 7.54 (s, 1 H) 7.62 (dd, J = 8.28, 1.76 Hz, 1 H) 10.05 (s, 1 H) 13 N-(3-((3,4-difluorophenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.68- [M − H]− 313 1.35 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.81 (m, 1 H) 2.44-2.48 (m, 1 H) 2.70- 2.82 (m, 1 H) 2.83-2.94 (m, 1 H) 4.92 (q, J = 7.53 Hz, 1 H) 5.71 (dd, J = 10.26, 2.18 Hz, 1 H) 6.15 (d, J = 8.53 Hz, 1 H) 6.22 (dd, J = 17.03, 2.18 Hz, 1 H) 6.40 (dd, J = 17.03, 10.26 Hz, 1 H) 6.45-6.52 (m, 1 H) 6.64- 6.72 (m, 1 H) 7.07-7.17 (m, 1 H) 7.20 (d, J = 8.78 Hz, 1 H) 7.50-7.66 (m, 2 H) 10.04 (s, 1 H) 14 N-(3-((3-fluoro-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.71- [M + H]+ 297 1.32 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.84 (m, 1 H) 2.52-2.56 (m, 1 H) 2.72- 2.82 (m, 1 H) 2.84-2.96 (m, 1 H) 4.96 (q, J = 7.53 Hz, 1 H) 5.71 (dd, J = 10.16, 2.15 Hz, 1 H) 6.21 (dd, J = 16.81, 2.15 Hz, 1 H) 6.26- 6.33 (m, 2 H) 6.40 (dd, J = 16.81, 10.16 Hz, 1 H) 6.46-6.58 (m, 2 H) 7.03-7.13 (m, 1 H) 7.20 (d, J = 8.03 Hz, 1 H) 7.54-7.66 (m, 2 H) 10.05 (s, 1 H) 15 N-(3-((4-fluoro-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.68- [M + H]+ 297 1.13 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.82 (m, 1 H) 2.43-2.47 (m, 1 H) 2.70- 2.82 (m, 1 H) 2.83-2.97 (m, 1 H) 4.90 (q, J = 7.61 Hz, 1 H) 5.70 (dd, J = 10.02, 2.05 Hz, 1 H) 5.82 (d, J = 8.53 Hz, 1 H) 6.21 (dd, J = 16.93, 2.05 Hz, 1 H) 6.40 (dd, J = 16.93, 10.02 Hz, 1 H) 6.62-6.80 (m, 2 H) 6.84- 6.98 (m, 2 H) 7.20 (d, J = 8.78 Hz, 1 H) 7.51- 7.68 (m, 2 H) 10.03 (s, 1 H) 16 N-(1-((3,4-difluorophenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.68- [M − H]− 313 1.31 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.83 (m, 1 H) 2.43-2.47 (m, 1 H) 2.74- 2.86 (m, 1 H) 2.88-2.99 (m, 1 H) 4.87 (q, J = 7.28 Hz, 1 H) 5.73 (dd, J = 10.16, 2.13 Hz, 1 H) 6.07 (d, J = 8.28 Hz, 1 H) 6.24 (dd, J = 17.07, 2.13 Hz, 1 H) 6.38-6.53 (m, 2 H) 6.62-6.72 (m, 1 H) 7.05-7.17 (m, 1 H) 7.21 (d, J = 8.28 Hz, 1 H) 7.40 (dd, J = 8.28, 1.51 Hz, 1 H) 7.66 (s, 1 H) 10.08 (s, 1 H) 17 N-(1-((3-methoxyphenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.71- [M − H]− 307 1.08 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.86 (m, 1 H) 2.42-2.46 (m, 1 H) 2.73- 2.85 (m, 1 H) 2.88-2.99 (m, 1 H) 3.67 (s, 3 H) 4.90 (q, J = 7.28 Hz, 1 H) 5.73 (dd, J = 10.04, 2.01 Hz, 1 H) 5.83 (d, J = 8.28 Hz, 1 H) 6.13 (dd, J = 8.16, 2.01 Hz, 1 H) 6.21- 6.35 (m, 3 H) 6.43 (dd, J = 17.05, 10.04 Hz, 1 H) 6.98 (t, J = 8.16 Hz, 1 H) 7.21 (d, J = 8.03 Hz, 1 H) 7.38 (dd, J = 8.03, 1.63 Hz, 1 H) 7.65 (s, 1 H) 10.06 (s, 1 H) 18 N-(1-(m-tolylamino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.70- [M − H]− 291 1.04 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.84 (m, 1 H) 2.19 (s, 3 H) 2.43-2.49 (m, 1 H) 2.73-2.85 (m, 1 H) 2.87-2.98 (m, 1 H) 4.90 (q, J = 7.28 Hz, 1 H) 5.63-5.81 (m, 2 H) 6.24 (dd, J = 17.06, 2.06 Hz, 1 H) 6.33-6.57 (m, 4 H) 6.96 (t, J = 7.78 Hz, 1 H) 7.20 (d, J = 8.28 Hz, 1 H) 7.38 (dd, J = 8.28, 1.63 Hz, 1 H) 7.65 (s, 1 H) 10.06 (s, 1 H) 19 N-(1-((6-fluoropyridin-3-yl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.71- [M + H]+ 298 1.05 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.83 (m, 1 H) 2.53-2.56 (m, 1 H) 2.77- 2.87 (m, 1 H) 2.90-3.02 (m, 1 H) 4.92 (q, J = 7.19 Hz, 1 H) 5.74 (dd, J = 10.33, 2.05 Hz, 1 H) 6.06 (d, J = 8.53 Hz, 1 H) 6.24 (dd, J = 16.97, 2.05 Hz, 1 H) 6.43 (dd, J = 16.97, 10.33 Hz, 1 H) 6.90 (dd, J = 8.78, 3.26 Hz, 1 H) 7.22 (d, J = 8.28 Hz, 1 H) 7.24-7.32 (m, 1 H) 7.41 (dd, J = 8.28, 1.51 Hz, 1 H) 7.61 (, 1 H) 7.67 (s, 1 H) 10.08 (s, 1 H) 20 N-(1-((6-(trifluoromethyl)-pyridin-3-yl)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.76- [M + H]+ 348 1.40 A amino)-2,3-dihydro-1H-inden-5-yl)- 1.88 (m, 1 H) 2.53-2.58 (m, 1 H) 2.79- acrylamide 2.90 (m, 1 H) 2.92-3.03 (m, 1 H) 5.05 (q, J = 7.03 Hz, 1 H) 5.74 (dd, J = 9.94, 2.21 Hz, 1 H) 6.24 (dd, J = 16.99, 2.21 Hz, 1 H) 6.43 (dd, J = 16.99, 9.94 Hz, 1 H) 6.95 (d, J = 8.03 Hz, 1 H) 7.14-7.27 (m, 2 H) 7.42 (dd, J = 8.28, 1.51 Hz, 1 H) 7.54 (d, J = 8.78 Hz, 1 H) 7.69 (s, 1 H) 8.16 (d, J = 2.76 Hz, 1 H) 10.10 (s, 1 H) 21 N-(1-((5-fluoropyridin-2-yl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.71- [M + H]+ 298 0.79 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.84 (m, 1 H) 2.42-2.46 (m, 1 H) 2.74- 2.85 (m, 1 H) 2.87-2.99 (m, 1 H) 5.36 (q, J = 7.53 Hz, 1 H) 5.73 (dd, J = 10.14, 1.97 Hz, 1 H) 6.23 (dd, J = 17.01, 1.97 Hz, 1 H) 6.42 (dd, J = 17.01, 10.14 Hz, 1 H) 6.55 (dd, J = 8.28, 3.64 Hz, 1 H) 6.79 (d, J = 8.03 Hz, 1 H) 7.17 (d, J = 8.28 Hz, 1 H) 7.31-7.42 (m, 2 H) 7.64 (s, 1 H) 7.96 (d, J = 3.01 Hz, 1 H) 10.05 (s, 1 H) 22 methyl-3-((5-acrylamido- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.73- [M − H]− 335 1.25 A 2,3-dihydro-1H-inden-1-yl)- 1.85 (m, 1 H) 2.51-2.55 (m, 1 H) 2.77- amino)benzoate 2.88 (m, 1 H) 2.88-3.00 (m, 1 H) 3.81 (s, 3 H) 4.95 (q, J = 7.11 Hz, 1 H) 5.74 (dd, J = 10.01, 1.83 Hz, 1 H) 6.15-6.31 (m, 2 H) 6.44 (dd, J = 16.64, 10.01 Hz, 1 H) 6.98 (ddd, J = 8.16, 2.380, 1.00 Hz, 1 H) 7.10-7.26 (m, 3 H) 7.28-7.35 (m, 1 H) 7.39 (dd, J = 8.16, 1.63 Hz, 1 H) 7.66 (s, 1 H) 10.07 (s, 1 H) 23 N-(3-(benzyl-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.73- [M + H]+ 293 0.55 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.85 (m, 1 H) 2.25-2.39 (m, 2 H) 2.62- 2.73 (m, 1 H) 2.81-2.93 (m, 1 H) 3.73- 3.87 (m, 2 H) 4.10 (br t, J = 6.78 Hz, 1 H) 5.72 (dd, J = 10.04, 2.01 Hz, 1 H) 6.24 (dd, J = 17.00, 2.01 Hz, 1 H) 6.43 (dd, J = 17.00, 10.04 Hz, 1 H) 7.15 (d, J = 8.03 Hz, 1 H) 7.22 (t, J = 7.55 Hz, 1 H) 7.32 (t, J = 7.53 Hz, 2 H) 7.41 (d, J = 7.03 Hz, 2 H) 7.49 (dd, J = 8.03, 1.76 Hz, 1 H) 7.69 (s, 1 H) 10.03 (s, 1 H) 24 N-(1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.75- [M + H]+ 361 0.66 A (trifluoromethyl)-benzyl)amino)- 1.86 (m, 1 H) 2.24-2.35 (m, 1 H) 2.65- 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.77 (m, 1 H) 2.87-2.98 (m, 1 H) 3.87 (br s, 2 H) 4.11 (br t, J = 6.15 Hz, 1 H) 5.72 (dd, J = 10.04, 2.01 Hz, 1 H) 6.23 (dd, J = 16.92, 2.01 Hz, 1 H) 6.43 (dd, J = 16.92, 10.04 Hz, 1 H) 7.31 (d, J = 8.03 Hz, 1 H) 7.41 (dd, J = 8.03, 1.63 Hz, 1 H) 7.51-7.62 (m, 4 H) 7.70 (d, J = 7.03 Hz, 1 H) 7.76 (s, 1 H) 10.02 (s, 1 H) 25 N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.68- [M + H]+ 361 0.66 A (trifluoromethyl)-benzyl)amino)- 1.93 (m, 1 H) 2.21-2.39 (m, 1 H) 2.55 (br s, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H) 2.62-2.79 (m, 1 H) 2.92 (m, 1 H) 3.87 (br s, 2 H) 4.10 (br t, J = 6.15 Hz, 1 H) 5.73 (dd, J = 10.01, 1.92 Hz, 1 H) 6.23 (dd, J = 17.04, 1.92 Hz, 1 H) 6.42 (dd, J = 17.04, 10.01 Hz, 1 H) 7.31 (d, J = 8.28 Hz, 1 H) 7.41 (dd, J = 8.28, 1.38 Hz, 1 H) 7.54-7.77 (m, 5 H) 10.03 (s, 1 H) 26 N-(2-(((cis)-4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.42- [M + H]+ 353 0.57 A (trifluoromethyl)-cyclohexyl)-amino)- 1.58 (m, 4 H) 1.60-1.81 (m, 5 H) 2.14- 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.30 (m, 1 H) 2.55-2.69 (m, 2 H) 2.87- 2.95 (m, 1 H) 2.96-3.10 (m, 2 H) 3.47- 3.60 (m, 1 H) 5.71 (dd, J = 10.16, 2.13 Hz, 1 H) 6.22 (dd, J = 17.00, 2.13 Hz, 1 H) 6.41 (dd, J = 17.00, 10.16 Hz, 1 H) 7.09 (d, J = 8.03 Hz, 1 H) 7.34 (dd, J = 8.03, 1.51 Hz, 1 H) 7.53 (s, 1 H) 9.96 (s, 1 H) 27 N-(2-(((trans)-4- 1H NMR (400 MHz, DMSO-d6) δ ppm 0.96- [M + H]+ 353 0.62 A (trifluoromethyl)-cyclohexyl)-amino)- 1.14 (m, 2 H) 1.20-1.38 (m, 2 H) 1.64- 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.04 (m, 5 H) 2.10-2.26 (m, 1 H) 2.40- 2.48 (m, 1 H) 2.53-2.65 (m, 2 H) 3.93- 3.10 (m, 2 H) 3.65 (quin, J = 7.03 Hz, 1 H) 5.71 (dd, J = 9.93, 2.13 Hz, 1 H) 6.22 (dd, J = 16.94, 2.13 Hz, 1 H) 6.41 (dd, J = 16.94, 9.93 Hz, 1 H) 7.09 (d, J = 8.03 Hz, 1 H) 7.34 (dd, J = 8.03, 1.51 Hz, 1 H) 7.52 (s, 1 H) 9.96 (s, 1 H) 28 N-(2-((4,4-difluorocyclo-hexyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.26- [M + H]+ 321 0.50 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.53 (m, 2 H) 1.65-1.90 (m, 5 H) 1.93- 2.15 (m, 2 H) 2.53-2.81 (m, 3 H) 2.95- 3.10 (m, 2 H) 3.60 (br s, 1 H) 5.71 (dd, J = 10.05, 2.01 Hz, 1 H) 6.22 (dd, J = 16.77, 2.01 Hz, 1 H) 6.41 (dd, J = 16.77, 10.05 Hz, 1 H) 7.10 (d, J = 8.28 Hz, 1 H) 7.34 (dd, J = 8.28, 1.51 Hz, 1 H) 7.53 (s, 1 H) 9.97 (s, 1 H) 29 N-(2-((4,4,4-trifluorobutyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.54- [M + H]+ 313 0.49 A 2,3-dihydro-1H-inden-5-yl)-acrylamide I.71 (m, 2 H) 1.93 (br s, 1 H) 2.17-2.38 (m, 2 H) 2.54-2.68 (m, 4 H) 3.01 (ddd, J = 15.75, II.610, 7.03 Hz, 2 H) 3.47 (quin, J = 6.59 Hz, 1 H) 5.71 (dd, J = 10.04, 2.01 Hz, 1 H) 6.22 (dd, J = 17.33, 2.01 Hz, 1 H) 6.42 (dd, J = 17.33, 10.04 Hz, 1 H) 7.10 (d, J = 8.28 Hz, 1 H) 7.34 (dd, J = 8.28, 1.51 Hz, 1 H) 7.54 (s, 1 H) 9.96 (s, 1 H) 30 N-(2-((3-fluoropropyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.65- [M + H]+ 263 0.36 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.87 (m, 2 H) 2.54-2.73 (m, 5 H) 3.02 (ddd, J = 15.69, 11.670, 7.03 Hz, 2 H) 3.49 (quin, J = 6.71 Hz, 1 H) 4.49 (td, J = 47.60, 6.36 Hz, 2 H) 5.71 (dd, J = 10.03, 2.01 Hz, 1 H) 6.22 (dd, J = 17.07, 2.01 Hz, 1 H) 6.41 (dd, J = 17.07, 10.03 Hz, 1 H) 7.10 (d, J = 8.28 Hz, 1 H) 7.34 (dd, J = 8.28, 1.76 Hz, 1 H) 7.54 (s, 1 H) 9.96 (s, 1 H) 31 N-(2-((3-fluorophenyl)-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.69- [M + H]+ 297 1.24 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.81 (m, 2 H) 3.20-3.29 (m, 2 H) 4.14- 4.28 (m, 1 H) 5.72 (dd, J = 10.06, 2.07 Hz, 1 H) 6.15-6.52 (m, 6 H) 7.07 (q, J = 8.03 Hz, 1 H) 7.16 (d, J = 8.28 Hz, 1 H) 7.40 (dd, J = 8.28, 1.51 Hz, 1 H) 7.59 (s, 1 H) 10.01 (s, 1 H) 32 N-(2-((3-(trifluoromethyl)-phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.70- [M + H]+ 347 1.39 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.82 (m, 2 H) 3.22-3.28 (m, 2 H) 4.20- 4.33 (m, 1 H) 5.72 (dd, J = 10.04, 2.01 Hz, 1 H) 6.23 (dd, J = 16.74, 2.01 Hz, 1 H) 6.36- 6.48 (m, 2 H) 6.76-6.93 (m, 3 H) 7.17 (d, J = 8.03 Hz, 1 H) 7.29 (t, J = 7.78 Hz, 1 H) 7.40 (dd, J = 8.03, 1.51 Hz, 1 H) 7.60 (s, 1 H) 10.02 (s, 1 H) 33 N-(3-(4,4,4-trifluorobutoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.65- [M + H]+ 314 1.28 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.81 (m, 2 H) 1.85-1.99 (m, 1 H) 2.22- 2.41 (m, 3 H) 2.65-2.78 (m, 1 H) 2.83- 2.99 (m, 1 H) 3.56 (t, J = 6.02 Hz, 2 H) 4.83- 4.92 (m, 1 H) 5.73 (dd, J = 10.14, 2.11 Hz, 1 H) 6.23 (dd, J = 16.99, 2.11 Hz, 1 H) 6.42 (dd, J = 16.99, 10.14 Hz, 1 H) 7.20 (d, J = 8.16 Hz, 1 H) 7.52 (dd, J = 8.16, 1.88 Hz, 1 H) 7.71 (d, J = 1.88 Hz, 1 H) 10.07 (s, 1 H) 34 N-(3-(4-fluorobutoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.54- [M + H]+ 278 1.13 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 1.81 (m, 4 H) 1.84-1.98 (m, 1 H) 2.26- 2.39 (m, 1 H) 2.62-2.76 (m, 1 H) 2.80- 2.99 (m, 1 H) 3.48-3.59 (m, 2 H) 4.45 (td, J = 47.72, 6.21 Hz, 2 H) 4.81-4.88 (m, 1 H) 5.73 (dd, J = 10.05, 2.04 Hz, 1 H) 6.24 (dd, J = 16.89, 2.04 Hz, 1 H) 6.42 (dd, J = 16.89, 10.05 Hz, 1 H) 7.19 (d, J = 8.03 Hz, 1 H) 7.51 (dd, J = 8.03, 2.01 Hz, 1 H) 7.71 (d, J = 2.01 Hz, 1 H) 10.07 (s, 1 H) 35 N-(3-((4,4-difluorocyclo-hexyl)oxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.65- [M + H]+ 322 1.28 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.14 (m, 9 H) 2.31-2.43 (m, 1 H) 2.64- 2.76 (m, 1 H) 2.83-2.96 (m, 1 H) 3.72- 3.82 (m, 1 H) 5.00 (t, J = 6.15 Hz, 1 H) 5.73 (dd, J = 10.01, 1.98 Hz, 1 H) 6.24 (dd, J = 16.85, 1.98 Hz, 1 H) 6.42 (dd, J = 16.85, 10.01 Hz, 1 H) 7.18 (d, J = 8.28 Hz, 1 H) 7.53 (dd, J = 8.28, 1.76 Hz, 1 H) 7.65 (s, 1 H) 10.06 (s, 1 H) 36 N-(3-(((trans)-4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.19- [M + H]+ 354 1.41 A (trifluoro-methyl)cyclo-hexyl)oxy)- 1.44 (m, 4 H) 1.77-1.96 (m, 3 H) 2.02- 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.18 (m, 2 H) 2.20-2.43 (m, 2 H) 2.62- 2.74 (m, 1 H) 2.79-2.95 (m, 1 H) 3.41- 3.55 (m, 1 H) 5.01 (t, J = 6.15 Hz, 1 H) 5.73 (dd, J = 10.14, 2.15 Hz, 1 H) 6.23 (dd, J = 16.95, 2.15 Hz, 1 H) 6.42 (dd, J = 16.95, 10.14 Hz, 1 H) 7.17 (d, J = 8.28 Hz, 1 H) 7.50 (dd, J = 8.28, 1.76 Hz, 1 H) 7.66 (d, J = 1.76 Hz, 1 H) 10.05 (s, 1 H) 37 N-(3-(4-(trifluoromethyl)-phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.97- [M + H]+ 348 1.63 A 38 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.10 (m, 1 H) 2.57-2.71 (m, 1 H) 2.80- [M + H]+ 280 1.28 A N-(3-phenoxy-2,3-dihydro-1H-inden-5-yl)- 2.92 (m, 1 H) 2.94-3.07 (m, 1 H) 5.73 (dd, acrylamide J = 10.09, 1.93 Hz, 1 H) 5.94-6.00 (m, 1 H) 6.23 (dd, J = 17.00, 1.93 Hz, 1 H) 6.41 (dd, J = 17.00, 10.09 Hz, 1 H) 7.23 (d, J = 8.53 Hz, 2 H) 7.28 (d, J = 8.28 Hz, 1 H) 7.60 (dd, J = 8.28, 1.88 Hz, 1 H) 7.68 (d, J = 8.53 Hz, 2 H) 7.77 (d, J = 1.88 Hz, 1 H) 10.12 (s, 1 H) 1H NMR (400 MHz, DMSO-d6) δ ppm 1.95- 2.08 (m, 1 H) 2.53-2.64 (m, 1 H) 2.78-2.91 (m, 1 H) 2.93-3.06 (m, 1 H) 5.73 (dd, J = 10.19, 2.10 Hz, 1 H) 5.79-5.86 (m, 1 H) 6.23 (dd, J = 17.06, 2.10 Hz, 1 H) 6.41 (dd, J = 17.06, 10.19 Hz, 1 H) 6.96 (t, J = 7.28 Hz, 1 H) 7.03 (d, J = 7.86 Hz, 2 H) 7.23-7.38 (m, 3 H) 7.58 (dd, J = 7.86, 1.88 Hz, 1 H) 7.74 (s, 1 H) 10.11 (s, 1 H) 39 N-(3-(3-(trifluoromethyl)-phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.97- [M + H]+ 348 1.47 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.09 (m, 1 H) 2.56-2.65 (m, 1 H) 2.78-2.91 (m, 1 H) 2.93-3.06 (m, 1 H) 5.73 (dd, J = 10.04, 2.12 Hz, 1 H) 5.95-6.01 (m, 1 H) 6.23 (dd, J = 16.96, 2.12 Hz, 1 H) 6.41 (dd, J = 16.96, 10.04 Hz, 1 H) 7.18-7.46 (m, 4 H) 7.50-7.65 (m, 2 H) 7.77 (d, J = 1.51 Hz, 1 H) 10.11 (s, 1 H) 40 N-(3-(3,4-difluorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.94- [M + H]+ 316 1.67 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.07 (m, 1 H) 2.53-2.63 (m, 1 H) 2.76- 2.89 (m, 1 H) 2.92-3.08 (m, 1 H) 5.73 (dd, J = 10.14, 2.16 Hz, 1 H) 5.81-5.88 (m, 1 H) 6.22 (dd, J = 16.83, 2.16 Hz, 1 H) 6.41 (dd, J = 16.83, 10.14 Hz, 1 H) 6.80-6.92 (m, 1 H) 7.12-7.23 (m, 1 H) 7.27 (d, J = 8.28 Hz, 1 H) 7.32-7.43 (m, 1 H) 7.58 (dd, J = 8.28, 1.88 Hz, 1 H) 7.75 (d, J = 1.88 Hz, 1 H) 10.10 (s, 1 H) 41 N-(3-(3-fluorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.95- [M + H]+ 298 1.33 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.06 (m, 1 H) 2.54-2.65 (m, 1 H) 2.78- 2.90 (m, 1 H) 2.93-3.05 (m, 1 H) 5.73 (dd, J = 10.04, 2.01 Hz, 1 H) 5.85-5.91 (m, 1 H) 6.23 (dd, J = 16.94, 2.02 Hz, 1 H) 6.41 (dd, J = 16.94, 10.04 Hz, 1 H) 6.73-6.83 (m, 1 H) 6.85-6.97 (m, 2 H) 7.27 (d, J = 8.28 Hz, 1 H) 7.30-7.38 (m, 1 H) 7.59 (dd, J = 8.28, 1.88 Hz, 1 H) 7.75 (d, J = 1.88 Hz, 1 H) 10.11 (s, 1 H) 42 N-(3-(4-fluorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.94- [M − H]− 296 1.32 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.06 (m, 1 H) 2.53-2.62 (m, 1 H) 2.77- 2.89 (m, 1 H) 2.93-3.06 (m, 1 H) 5.73 (dd, J = 10.06, 2.02 Hz, 1 H) 5.76-5.82 (m, 1 H) 6.23 (dd, J = 16.93, 2.02 Hz, 1 H) 6.41 (dd, J = 16.93, 10.06 Hz, 1 H) 7.01-7.08 (m, 2 H) 7.11-7.20 (m, 2 H) 7.26 (d, J = 8.28 Hz, 1 H) 7.57 (dd, J = 8.28, 1.88 Hz, 1 H) 7.74 (d, J = 1.88 Hz, 1 H) 10.10 (s, 1 H) 43 N-(3-(3,5-difluorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.95- [M + H]+ 316 1.37 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.06 (m, 1 H) 2.53-2.65 (m, 1 H) 2.78- 2.89 (m, 1 H) 2.92-3.07 (m, 1 H) 5.73 (dd, J = 10.06, 1.98 Hz, 1 H) 5.89-5.95 (m, 1 H) 6.23 (dd, J = 17.03, 1.98 Hz, 1 H) 6.41 (dd, J = 17.03, 10.06 Hz, 1 H) 6.70-6.92 (m, 3 H) 7.27 (d, J = 8.03 Hz, 1 H) 7.58 (dd, J = 8.03, 2.01 Hz, 1 H) 7.76 (d, J = 2.01 Hz, 1 H) 10.12 (s, 1 H) 44 N-(3-(2,4-difluorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.01- [M + H]+ 316 1.31 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.13 (m, 1 H) 2.53-2.59 (m, 1 H) 2.77- 2.89 (m, 1 H) 2.96-3.07 (m, 1 H) 5.73 (dd, J = 10.04, 2.01 Hz, 1 H) 5.78-5.84 (m, 1 H) 6.23 (dd, J = 17.02, 2.01 Hz, 1 H) 6.41 (dd, J = 17.02, 10.04 Hz, 1 H) 6.99-7.11 (m, 1 H) 7.22-7.43 (m, 3 H) 7.59 (dd, J = 8.28, 1.76 Hz, 1 H) 7.74 (d, J = 1.76 Hz, 1 H) 10.11 (s, 1 H) 45 N-(1-(3-(trifluoromethyl)-phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.98- [M + H]+ 348 1.44 A 2,3-dihydro-1H-inden-5-yl)-acrylamide 2.13 (m, 1 H) 2.54-2.63 (m, 1 H) 2.84- 2.94 (m, 1 H) 2.99-3.11 (m, 1 H) 5.76 (dd, J = 9.66, 2.38 Hz, 1 H) 5.89-5.96 (m, 1 H) 6.26 (dd, J = 2.38, 17.04 Hz, 1 H) 6.44 (dd, J = 17.04, 9.66 Hz, 1 H) 7.25-7.39 (m, 4 H) 7.46 (dd, J = 8.28, 1.76 Hz, 1 H) 7.55 (t, J = 8.09 Hz, 1 H) 7.73 (s, 1 H) 10.16 (s, 1 H) 46 N-(1-(3-(trifluoro-methoxy)-phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.04 [M + H]+ 364 1.48 A 2,3-dihydro-1H-inden-5-yl)-acrylamide (dddd, J = 13.55, 8.530, 4.770, 3.76 Hz, 1 H) 2.52-2.61 (m, 1 H) 2.87 (ddd, J = 16.12, 8.720, 4.77 Hz, 1 H) 2.96-3.12 (m, 1 H) 5.76 (dd, J = 10.03, 2.02 Hz, 1 H) 5.87 (dd, J = 6.53, 3.51 Hz, 1 H) 6.26 (dd, J = 16.87, 2.02 Hz, 1 H) 6.44 (dd, J = 16.87, 10.03 Hz, 1 H) 6.94 (dt, J = 8.28, 1.00 Hz, 1 H) 7.01 (s, 1 H) 7.06-7.16 (m, 1 H) 7.34 (d, J = 8.28 Hz, 1 H) 7.39-7.51 (m, 2 H) 7.73 (s, 1 H) 10.15 (s, 1 H) 47 methyl 3-[6-(prop-2-enoyl-amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.97- [M + H]+ 338 1.29 A 2,3-dihydro-1H-inden-1-yl]-oxybenzoate 2.11 (m, 1 H) 2.55-2.65 (m, 1 H) 2.79- 2.92 (m, 1 H) 2.95-3.07 (m, 1 H) 3.86 (s, 3 H) 5.73 (dd, J = 10.23, 2.12 Hz, 1 H) 5.92 (dd, J = 6.57, 4.57 Hz, 1 H) 6.23 (dd, J = 17.05, 2.12 Hz, 1 H) 6.41 (dd, J = 17.05, 10.23 Hz, 1 H) 7.28 (d, J = 8.25 Hz, 1 H) 7.34 (ddd, J = 8.25, 2.720, 1.06 Hz, 1 H) 7.48 (t, J = 7.88 Hz, 1 H) 7.53-7.64 (m, 3 H) 7.75 (d, J = 1.63 Hz, 1 H) 10.12 (s, 1 H) 48 N-(2-((3-fluorophenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.70- [M + H]+ 297 1.63 D 2,3-dihydro-1H-inden-5-yl)acrylamide 2.80 (m, 2 H), 3.20-3.29 (m, 2 H), 4.20 (sxt, Enantiomer 1 J = 6 Hz, 1 H), 5.73 (d, J = 10 Hz, 1 H), 6.20- 6.46 (m, 6 H), 7.07 (q, J = 8 Hz, 1 H), 7.17 (d, J = 8 Hz, 1 H), 7.40 (d, J = 8 Hz, 1 H), 7.60 (s, 1 H), 10.04(s, 1 H) 49 N-(2-((3-fluorophenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.69- [M + H]+ 297 1.63 D 2,3-dihydro-1H-inden-5-yl)acrylamide 2.81 (m, 2 H), 3.20-3.30 (m, 2 H), 4.20 (sxt, Enantiomer 2 J = 6 Hz, 1 H), 5.73 (d, J = 10 Hz, 1 H), 6.21- 6.46 (m, 6 H), 7.07 (q, J = 8 Hz, 1 H), 7.17 (d, J = 8 Hz, 1 H), 7.40 (d, J = 8 Hz, 1 H), 7.60 (s, 1 H), 10.04(s, 1 H) 50 N-(2-((3-(trifluoromethyl)phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.77 [M + H]+ 347 1.80 D 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 2 H), 3.28 (m, 2 H), 4.27 (ddt, J = 12, 7, 6, Enantiomer 1 6 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.42 (m, 2 H), 6.76- 6.95 (m, 3 H), 7.18 (d, J = 8 Hz, 1 H), 7.30 (t, J = 8 Hz, 1 H), 7.41 (d, J = 8 Hz, 1 H), 7.61 (s, 1 H), 10.05 (s, 1 H) 51 N-(2-((3-(trifluoromethyl)phenyl)amino)- 1H NMR (500 MHz, DMSO-d6) δ ppm 2.76 [M + H]+ 347 1.85 D 2,3-dihydro-1H-inden-5-yl)acrylamide (td, J = 17, 5 Hz, 2 H), 3.21-3.37 (m, 2 H), Enantiomer 2 4.27 (dquin, J = 7, 6, 6, 6, 6 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.37-6.50 (m, 2 H), 6.81 (d, J = 8 Hz, 1 H), 6.84-6.93 (m, 2 H), 7.17 (d, J = 8 Hz, 1 H), 7.29 (t, J = 8 Hz, 1 H), 7.40 (d, J = 8 Hz, 1 H), 7.60 (s, 1 H), 10.03 (s, 1 H) 52 N-[2-[4-(trifluoromethyl)anilino]- 1H NMR (500 MHz, DMSO-d6) δ ppm 2.79 [M + H]+ 347 1.38 A 2,3-dihydro-1H-inden-5-yl]acrylamide (td, J = 16, 5 Hz, 2 H), 3.28 (m, 2 H), 4.28 (m, 1 H), 5.73 (d, J = 10 Hz, 1 H), 6.24 (d, J = 17 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 6.63 (d, J = 6 Hz, 1 H), 6.73 (d, J = 8 Hz, 2 H), 7.18 (d, J = 8 Hz, 1 H), 7.39 (m, 3 H), 7.61 (s, 1 H), 10.03 (s, 1 H) 53 N-(3-((3,5-difluorophenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.76 [M − H]− 313 1.35 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.41 (m, 1 H), 2.77 (m, 1 H), 2.89 (m, 1 H), 4.98 (m, 1 H), 5.71 (dd, J = 10, 2 Hz, 1 H), 6.18-6.27 (m, 2 H), 6.32-6.44 (m, 3 H), 6.63 (br s, 1 H), 7.21 (d, J = 8 Hz, 1 H), 7.58 (m, 2 H), 10.06 (s, 1 H) 54 N-(1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.79 [M − H]− 403 1.47 A (pentafluoro-l6-sulfanyl)phenyl)amino)- (m, 1 H), 2.55 (m hidden, 1 H), 2.80-3.0 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 2 H), 4.98 (q, J = 7 Hz, 1 H), 5.75 (d, J = 11 Hz, 1 H), 6.26 (m, 1 H), 6.47 (m, 2 H), 6.97 (m, 2 H), 7.16 (br s, 1 H), 7.22 (d, J = 8 Hz, 1 H), 7.31 (t, J = 8 Hz, 1 H), 7.42 (d, J = 8 Hz, 1 H), 7.68 (s, 1 H), 10.10 (s, 1 H) 55 N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.81 [M + H]+ 347 1.84 D (trifluoromethyl)phenyl)amino)- (m, 1 H), 2.54 (m, 1 H), 2.83 (dt, J = 16, 8 Hz, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H), 2.95 (ddd, J = 16, 9, 4 Hz, 1 H), 5.00 (q, Enantiomer 1 J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.43 (dd, J = 17, 10 Hz, 1 H), 6.67 (d, J = 8 Hz, 1 H), 6.82 (d, J = 9 Hz, 2 H), 7.21 (d, J = 8 Hz, 1 H), 7.39 (m, 3 H), 7.69 (s, 1 H), 10.11 (s, 1 H) 56 N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.81 [M + H]+ 347 1.84 D (trifluoromethyl)phenyl)amino)- (m, 1 H), 2.54 (m, 1 H), 2.83 (dt, J = 16, 8 Hz, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H), 2.95 (ddd, J = 16, 9, 4 Hz, 1 H), 5.00 (q, Enantiomer 2 J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.43 (dd, J = 17, 10 Hz, 1 H), 6.67 (d, J = 8 Hz, 1 H), 6.82 (d, J = 9 Hz, 2 H), 7.21 (d, J = 8 Hz, 1 H), 7.39 (m, 3 H), 7.69 (s, 1 H), 10.11 (s, 1 H) 57 N-[(1S)-1-[[4- 1H NMR (500 MHz, DMSO-d6) δ ppm 1.82 [M + H]+ 348 1.53 D (trifluoromethyl)pyridin-2-yl]amino]- (dq, J = 13, 8 Hz, 1 H), 2.55 (m hidden, 1 H), 2,3-dihydro-1H-inden-5-yl]acrylamide 2.83 (dt, J = 16, 8 Hz, 1 H), 2.95 (ddd, J = 16, 9, 4 Hz, 1 H), 5.50 (q, J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.75 (d, J = 5 Hz, 1 H), 6.81 (s, 1 H), 7.20 (d, J = 8 Hz, 1 H), 7.40 (m, 2 H), 7.68 (s, 1 H), 8.24 (d, J = 5 Hz, 1 H), 10.09 (s, 1 H) 58 N-[(1 R)-1-[[4- 1H NMR (500 MHz, DMSO-d6) δ ppm 1.82 [M + H]+ 348 1.53 D (trifluoromethyl)pyridin-2-yl]amino]- (dq, J = 13, 8 Hz, 1 H), 2.55 (m hidden, 1 H), 2,3-dihydro-1H-inden-5-yl]acrylamide 2.83 (dt, J = 16, 8 Hz, 1 H), 2.95 (ddd, J = 16, 9, 4 Hz, 1 H), 5.50 (q, J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.75 (d, J = 5 Hz, 1 H), 6.81 (s, 1 H), 7.20 (d, J = 8 Hz, 1 H), 7.40 (m, 2 H), 7.68 (s, 1 H), 8.24 (d, J = 5 Hz, 1 H), 10.09 (s, 1 H) 59 N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm [M + H]+ 348 1.14 A (trifluoromethyl)pyridin-2-yl)amino)- 1.83(m, 1 H), 2.57 (m, 1 H), 2.83 (dt, J = 16, 8 2,3-dihydro-1H-inden-5-yl)acrylamide Hz, 1 H), 2.96 (ddd, J = 16, 9, 4 Hz, 1 H), 2,2,2-trifluoroacetate 5.48 (t, J = 6 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.79 (d, J = 5 Hz, 1 H), 6.88 (s, 1 H), 7.21 (d, J = 8 Hz, 1 H), 7.41 (br d, J = 7 Hz, 1 H), 7.61 (br s, 1 H), 7.68 (s, 1 H), 8.24 (d, J = 5 Hz, 1 H), 10.09 (s, 1 H) 60 N-(1-((6-(trifluoromethyl)pyridin- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.84 [M + H]+ 348 1.35 A 2-yl)amino)- (m, 1 H), 2.55 (m hidden, 1 H), 2.83 (m, 1 2,3-dihydro-1H-inden-5-yl)acrylamide H), 2.95 (m, 1 H), 5.41 (q, J = 7 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.43 (dd, J = 17, 10 Hz, 1 H), 6.78 (d, J = 9 Hz, 1 H), 6.93 (d, J = 7 Hz, 1 H), 7.19 (d, J = 8 Hz, 1 H), 7.39 (t, J = 9 Hz, 2 H), 7.58 (t, J = 8 Hz, 1 H), 7.65 (s, 1 H), 10.06 (s, 1 H) 61 N-(1-((5-(trifluoromethyl)pyridin- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.79 [M + H]+ 348 1.12 A 3-yl)amino)- (m, 1 H), 2.56 (m, 1 H), 2.84 (m, 1 H), 2.96 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 5.08 (q, J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.71 (d, J = 8 Hz, 1 H), 7.22 (d, J = 8 Hz, 1 H), 7.31 (t, J = 2 Hz, 1 H), 7.43 (d, J = 8 Hz, 1 H), 7.69 (s, 1 H), 8.08 (s, 1 H), 8.33 (d, J = 2 Hz, 1 H), 10.10 (s, 1 H) 62 N-(1-(methyl(3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.90 [M − H]− 359 1.51 A (trifluoromethyl)phenyl)amino)- (dq, J = 13, 8 Hz, 1 H), 2.40 (m, 1 H), 2.61 (s, 2,3-dihydro-1H-inden-5-yl)acrylamide 3 H), 2.77-3.01 (m, 2 H), 5.60 (t, J = 8 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.96 (d, J = 8 Hz, 1 H), 7.04 (d, J = 8 Hz, 1 H), 7.10 (s, 1 H), 7.21 (dd, J = 8, 2 Hz, 1 H), 7.42 (m, 2 H), 7.69 (s, 1 H), 10.10 (s, 1 H) 63 N-(1-(methyl(phenyl)amino)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.88 [M − H]− 291 2.96 B 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.37 (m, 1 H), 2.54 (s, 3 H), 2.78- 2.99 (m, 2 H), 5.51 (t, J = 8 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.66 (t, J = 7 Hz, 1 H), 6.92 (d, J = 8 Hz, 2 H), 7.04 (d, J = 8 Hz, 1 H), 7.20 (dd, J = 9, 7 Hz, 2 H), 7.42 (d, J = 8 Hz, 1 H), 7.68 (s, 1 H), 10.08 (s, 1 H) 64 N-(1-(methyl(4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.91 [M − H]− 359 1.52 A (trifluoromethyl)phenyl)amino)- (m, 1 H), 2.42 (m, 1 H), 2.62 (s, 3 H), 2.86 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.98 (m, 1 H), 5.62 (t, J = 8 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.44 (dd, J = 17, 10 Hz, 1 H), 6.99-7.08 (m, 3 H), 7.43 (br d, J = 8 Hz, 1 H), 7.49 (d, J = 9 Hz, 2 H), 7.70 (s, 1 H), 10.10 (s, 1 H) 65 N-(3,3-dimethyl- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.23 [M − H]− 373 1.54 A 1-((3-(trifluoromethyl)phenyl)amino)- (s, 3 H), 1.33 (s, 3 H), 1.72 (dd, J = 12, 7 Hz, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H), 2.40 (dd, J = 12, 7 Hz, 1 H), 5.05 (q, J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.33-6.49 (m, 2 H), 6.82 (d, J = 8 Hz, 1 H), 6.98 (t, J = 2 Hz, 2 H), 7.17 (d, J = 8 Hz, 1 H), 7.29 (t, J = 8 Hz, 1 H), 7.45 (d, J = 8 Hz, 1 H), 7.60 (s, 1 H), 10.12 (s, 1 H) 66 N-(3,3-dimethyl- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.23 [M − H]− 373 1.53 A 1-((4-(trifluoromethyl)phenyl)amino)- (s, 3 H), 1.33 (s, 3 H), 1.74 (dd, J = 12, 8 Hz, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H), 2.40 (dd, J = 12, 7 Hz, 1 H), 5.06 (q, J = 7 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.43 (dd, J = 17, 10 Hz, 1 H), 6.64 (d, J = 8 Hz, 1 H), 6.83 (d, J = 9 Hz, 2 H), 7.16 (d, J = 8 Hz, 1 H), 7.39 (d, J = 9 Hz, 2 H), 7.44 (dd, J = 8, 1 Hz, 1 H), 7.61 (s, 1 H), 10.12 (s, 1 H) 67 N-[7-fluoro-1-[3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.93 [M − H]− 363 1.44 A (trifluoromethyl)anilino]- (m, 1 H), 2.41 (m, 1 H), 2.85 (ddd, J = 16, 9, 5 2,3-dihydro-1H-inden-5-yl]acrylamide Hz, 1 H), 3.06 (dt, J = 16, 8 Hz, 1 H), 5.14 (td, J = 8, 4 Hz, 1 H), 5.78 (dd, J = 10, 2 Hz, 1 H), 6.27 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 2 H), 6.81 (d, J = 8 Hz, 1 H), 6.92 (m, 2 H), 7.28 (t, J = 8 Hz, 1 H), 7.37 (d, J = 2 Hz, 1 H), 7.42 (dd, J = 12, 2 Hz, 1 H), 10.29 (s, 1 H) 68 N-[4-fluoro-1-[4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.88 [M − H]− 363 1.43 A (trifluoromethyl)anilino]- (m, 1 H), 2.57 (m, 1 H), 2.87 (m, 1 H), 3.03 2,3-dihydro-1H-inden-5-yl]acrylamide (m, 1 H), 5.09 (q, J = 7 Hz, 1 H), 5.76 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.58 (dd, J = 17, 10 Hz, 1 H), 6.72 (d, J = 8 Hz, 1 H), 6.83 (d, J = 9 Hz, 2 H), 7.06 (d, J = 8 Hz, 1 H), 7.40 (d, J = 9 Hz, 2 H), 7.71 (t, J = 8 Hz, 1 H), 9.88 (s, 1 H) 69 N-methyl-N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.85 [M + H]+ 361 1.48 A (trifluoromethyl)phenyl)amino)- (m, 1 H), 2.59 (m, 1 H), 2.81-3.07 (m, 2 H), 2,3-dihydro-1H-inden-5- 3.23 (s, 3 H), 5.08 (q, J = 7 Hz, 1 H), 5.57 (m, yl)acrylamide 1 H), 6.04-6.22 (m, 2 H), 6.72 (d, J = 8 Hz, 1 H), 6.85 (d, J = 9 Hz, 2 H), 7.08 (d, J = 8 Hz, 1 H), 7.21 (s, 1 H), 7.32 (d, J = 8 Hz, 1 H), 7.40 (d, J = 9 Hz, 2 H) 70 N-(3-((4,4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.43- [M + H]+ 321 0.52 A difluorocyclohexyl)amino)- 1.55 (m, 2 H), 1.60-1.94 (m, 6 H), 1.99- 2,3-dihydro-1H-inden-5-yl)acrylamide 2.15 (m, 2 H), 2.37(m, 1 H), 2.66 (m, 1 H), 2.79-2.90 (m, 2 H), 4.17 (q, J = 7 Hz, 1 H), 5.72 (dd, J = 10, 2 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 7.13 (d, J = 8 Hz, 1 H), 7.52 (br d, J = 8 Hz, 1 H), 7.59 (s, 1 H), 10.02 (s, 1 H) 71 N-(3-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.59 [M + H]+ 340 1.34 A (trifluoromethyl)cyclopentyl)oxy)- (m, 1 H), 1.70-1.91 (m, 5 H), 2.24 (m, 1 2,3-dihydro-1H-inden-5-yl)acrylamide H), 2.35 (m, 1 H), 2.68 (m, 1 H), 2.77-2.92 (m, 2 H), 4.17 (m, 1 H), 4.92 (t, J = 6 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 7.18 (d, J = 8 Hz, 1 H), 7.53 (dd, J = 8, 2 Hz, 1 H), 7.64 (dd, J = 5, 2 Hz, 1 H), 10.07 (br s, 1 H) 72 N-(3-((5,5,5-trifluoropentyl)oxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.48- [M + H]+ 328 1.32 A 2,3-dihydro-1H-inden-5-yl)acrylamide 1.66 (m, 4 H), 1.92 (m, 1 H), 2.18-2.38 (m, 3 H), 2.69 (m, 1 H), 2.89 (m, 1 H), 3.53 (t, J = 6 Hz, 2 H), 4.85 (t, J = 6 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 7.19 (d, J = 8 Hz, 1 H), 7.49 (dd, J = 9, 2 Hz, 1 H), 7.72 (s, 1 H), 10.07 (s, 1 H) 73 N-(3-(4,4-difluorobutoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.54- [M + H]+ 296 1.17 A 2,3-dihydro-1H-inden-5-yl)acrylamide 1.74 (m, 2 H), 1.78-1.99 (m, 3 H), 2.33 (m, 1 H), 2.70 (m, 1 H), 2.89 (m, 1 H), 3.50- 3.60 (m, 2 H), 4.86 (t, J = 6 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.09 (tt, J = 56, 4 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 7.20 (d, J = 8 Hz, 1 H), 7.51 (d, J = 7 Hz, 1 H), 7.71 (s, 1 H), 10.07 (s, 1 H) 74 N-(3-(2,2,2-trifluoroethoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.99 [M + H]+ 286 1.14 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.36 (m, 1 H), 2.72 (m, 1 H), 2.92 (m, 1 H), 4.07-4.21 (m, 2 H), 5.09 (dd, J = 6, 5 Hz, 1 H), 5.74 (dd, J = 10, 2 Hz, 1 H), 6.25 (dd, J = 17, 2 Hz, 1 H), 6.42 (dd, J = 17, 10 Hz, 1 H), 7.23 (d, J = 8 Hz, 1 H), 7.55 (dd, J = 8, 2 Hz, 1 H), 7.75 (s, 1 H), 10.11 (s, 1 H) 75 N-(3-(3,3,3-trifluoropropoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.92 [M + H]+ 300 1.18 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.33 (m, 1 H), 2.52-2.61 (m, 2 H), 2.71 (m, 1 H), 2.90 (m, 1 H), 3.72 (m, 2 H), 4.92 (dd, J = 6, 5 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.24 (dd, J = 17, 2 Hz, 1 H), 6.43 (dd, J = 17, 10 Hz, 1 H), 7.20 (d, J = 8 Hz, 1 H), 7.52 (dd, J = 8, 2 Hz, 1 H), 7.72 (s, 1 H), 10.09 (s, 1 H) 76 N-methyl-N-(1-((4- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.31 [M + H]+ 368 1.56 A (trifluoromethyl)cyclohexyl)oxy)- (m, 1 H), 1.48-1.69 (m, 4 H) 1.74-2.21 (m, 1.52 2,3-dihydro-1H-inden-5-yl)acrylamide 4 H) 2.24-2.46 (m, 2 H), 2.78 (m, 1 H), 2.96 (m, 1 H), 3.24 (s, 3 H), 3.86 (br s, 1 H), 4.99 (br t, J = 6 Hz, 1 H), 5.56 (br d, J = 12 Hz, 1 H), 6.13 (m, 2 H), 7.13 (m, 2 H), 7.36 (m, 1 H) 77 N-(3-(4-chlorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.00 [M − H]− 312 1.40 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.57 (m, 1 H), 2.83 (m, 1 H), 2.98 (m, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 5.84 (dd, J = 7, 5 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 7.07 (d, J = 9 Hz, 2 H), 7.27 (d, J = 8 Hz, 1 H), 7.36 (dd, J = 10, 1 Hz, 2 H), 7.58 (dd, J = 8, 2 Hz, 1 H), 7.74 (s, 1 H), 10.11 (s, 1 H) 78 N-(3-(3-chlorophenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.00 [M + H]+ 314 1.39 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.59 (m, 1 H), 2.84 (m, 1 H), 2.98 (m, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 5.90 (dd, J = 6, 5 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 7.02 (dd, J = 8, 2 Hz, 2 H), 7.12 (t, J = 2 Hz, 1 H), 7.27 (d, J = 8 Hz, 1 H), 7.34 (t, J = 8 Hz, 1 H), 7.58 (d, J = 8 Hz, 1 H), 7.75 (s, 1 H), 10.12 (s, 1 H) 79 N-(3-(m-tolyloxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 1.84 [M + H]+ 294 1.19 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.27 (s, 3 H), 2.44 (m, 1 H), 2.68 (m, 1 H), 2.75-3.00 (m, 2 H), 5.68 (dd, J = 10, 2 Hz, 1 H), 6.18 (dd, J = 17, 2 Hz, 1 H), 6.36 (dd, J = 17, 10 Hz, 1 H), 6.50 (dd, J = 8, 2 Hz, 1 H), 6.61 (d, J = 3 Hz, 1 H), 6.67 (d, J = 8 Hz, 1 H), 7.16 (s, 1 H), 7.21 (d, J = 8 Hz, 1 H), 7.50 (d, J = 8 Hz, 1 H), 7.63 (m, 1 H), 9.95 (s, 1 H) 80 N-(3-(3-(methylthio)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.01 [M + H]+ 326 1.38 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.47 (s, 3 H), 2.57 (m, 1 H), 2.83 (m, 1 H), 2.98 (m, 1 H), 5.73 (dd, J = 10, 3 Hz, 1 H), 5.87 (dd, J = 7, 4 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 6.85 (m, 3 H), 7.25 (m, 2 H), 7.58 (dd, J = 8, 2 Hz, 1 H), 0.00 (d, J = 9 Hz, 1 H), 10.11 (s, 1 H) 81 N-(3-(3-cyclopropylphenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 0.68 [M + H]+ 320 1.44 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 2 H), 0.93 (m, 2 H), 1.84-2.05 (m, 2 H), 2.60 (m, 1 H), 2.82 (m hidden, 1 H), 2.97 (m, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 5.82 (t, J = 6 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 6.63-6.74 (m, 2 H), 6.74-6.87 (m, 1 H), 7.17 (t, J = 8 Hz, 1 H), 7.26 (d, J = 8 Hz, 1 H), 7.50-7.69 (m, 1 H), 7.73 (s, 1 H), 10.10 (s, 1 H) 82 N-(1-(4-(trifluoromethyl)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.06 [M + H]+ 348 1.43 A 2,3-dihydro-1H-inden-5-yl)acrylamide (ddt, J = 13, 9, 4, 4 Hz, 1 H), 2.59 (m, 1 H), 2.90 (m, 1 H), 3.05 (m, 1 H), 5.76 (dd, J = 10, 2 Hz, 1 H), 5.93 (dd, J = 6, 3 Hz, 1 H), 6.27 (dd, J = 17, 2 Hz, 1 H), 6.45 (dd, J = 17, 10 Hz, 1 H), 7.22 (d, J = 9 Hz, 2 H), 7.36 (d, J = 8 Hz, 1 H), 7.47 (d, J = 8 Hz, 1 H), 7.67 (m, J = 9 Hz, 2 H), 7.75 (s, 1 H), 10.17 (s, 1 H) 83 N-methyl-N-(1-(4- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.09 [M + H]+ 362 1.52 A (trifluoromethyl)phenoxy)- (m, 1 H), 2.65 (m, 1 H), 2.93 (m, 1 H), 3.06 2,3-dihydro-1H-inden-5-yl)acrylamide (dd, J = 8, 6 Hz, 1 H), 3.25 (s, 3 H), 5.58 (m, 1 H), 5.99 (dd, J = 7, 4 Hz, 1 H), 6.05-6.22 (m, 2 H), 7.14 (dd, J = 8, 2 Hz, 1 H), 7.25 (d, J = 9 Hz, 2 H), 7.27 (d, J = 2 Hz, 1 H), 7.48 (d, J = 8 Hz, 1 H), 7.68 (d, J = 8 Hz, 2 H) 84 N-(1-(3-(trifluoromethyl)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.04 [M + H]+ 348 1.85 D 2,3-dihydro-1H-inden-5-yl)acrylamide (qd, J = 9, 5 Hz, 1 H), 2.57 (m, 1 H), 2.88 (m, Enantiomer 1 1 H), 3.05 (dt, J = 15, 8 Hz, 1 H), 5.76 (dd, J = 10, 2 Hz, 1 H), 5.94 (dd, J = 7, 3 Hz, 1 H), 6.26 (dd, J = 17, 2 Hz, 1 H), 6.45 (dd, J = 17, 10 Hz, 1 H), 7.33 (m, 4 H), 7.46 (d, J = 8 Hz, 1 H), 7.55 (t, J = 8 Hz, 1 H), 7.74 (s, 1 H), 10.18 (s, 1 H) 85 N-(1-(3-(trifluoromethyl)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.04 [M + H]+ 348 1.85 D 2,3-dihydro-1H-inden-5-yl)acrylamide (ddt, J = 13, 9, 4, 4 Hz, 1 H), 2.58 (m, 1 H), Enantiomer 2 2.88 (m, 1 H), 3.04 (m, 1 H), 5.76 (dd, J = 10, 2 Hz, 1 H), 5.94 (dd, J = 6, 3 Hz, 1 H), 6.26 (dd, J = 17, 2 Hz, 1 H), 6.45 (dd, J = 17, 10 Hz, 1 H), 7.28-7.38 (m, 4 H), 7.46 (d, J = 8 Hz, 1 H), 7.55 (t, J = 8 Hz, 1 H), 7.74 (s, 1 H), 10.18 (s, 1 H) 86 N-(3-(4-(trifluoromethyl)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.03 [M + H]+ 348 1.46 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.63 (m, 1 H), 2.86 (m, 1 H), 3.00 Enantiomer 1 (m, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 5.97 (dd, J = 6, 4 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 7.23 (d, J = 9 Hz, 2 H), 7.28 (d, J = 8 Hz, 1 H), 7.60 (dd, J = 8, 2 Hz, 1 H), 7.68 (d, J = 9 Hz, 2 H), 7.76 (s, 1 H), 10.12 (s, 1 H) 87 N-(3-(4-(trifluoromethyl)phenoxy)- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.03 [M + H]+ 348 1.45 A 2,3-dihydro-1H-inden-5-yl)acrylamide (m, 1 H), 2.64 (m, 1 H), 2.86 (m, 1 H), 3.00 Enantiomer 2 (m, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 5.97 (dd, J = 7, 4 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 7.23 (d, J = 9 Hz, 2 H), 7.28 (d, J = 8 Hz, 1 H), 7.60 (dd, J = 8, 2 Hz, 1 H), 7.68 (d, J = 9 Hz, 2 H), 7.76 (s, 1 H), 10.12 (s, 1 H) 88 N-[3-[5-(trifluoromethyl)pyridin- 1H NMR (500 MHz, DMSO-d6) δ ppm 2.10 [M + H]+ 349 1.41 A 2-yl]oxyindan-5-yl]prop-2-enamide (m, 1 H), 2.61 (m, 1 H), 2.86 (m, 1 H), 3.02 (m, 1 H), 5.72 (m, 1 H), 6.22 (dd, J = 17, 2 Hz, 1 H), 6.40 (dd, J = 17, 10 Hz, 1 H), 6.56 (dd, J = 7, 4 Hz, 1 H), 7.00 (d, J = 9 Hz, 1 H), 7.28 (d, J = 8 Hz, 1 H), 7.61 (dd, J = 8, 2 Hz, 1 H), 7.75 (s, 1 H), 8.08 (dd, J = 9, 3 Hz, 1 H), 8.66 (m, 1 H), 10.07 (s, 1 H) 89 N-methyl-N-(1-(3- 1H NMR (400 MHz, DMSO-d6) δ ppm 2.08 [M + H]+ 362 1.53 A (trifluoromethyl)phenoxy)- (qd, J = 9, 5 Hz, 1 H), 2.64 (m, 1 H), 2.93 (m, 2,3-dihydro-1H-inden-5-yl)acrylamide 1 H), 3.07 (m, 1 H), 3.25 (s, 3 H), 5.58 (m, 1 H), 6.00 (dd, J = 6, 4 Hz, 1 H), 6.14 (m, 2 H), 7.14 (d, J = 8 Hz, 1 H), 7.27 (s, 1 H), 7.33 (m, 2 H), 7.38 (d, J = 8 Hz, 1 H), 7.47 (d, J = 8 Hz, 1 H), 7.57 (t, J = 7 Hz, 1 H) 90 N-[2-fluoro-3-[4- 1H NMR (400 MHz, DMSO-d6) δ ppm 3.11 [M + H]+ 365 1.34 A (trifluoromethyl)anilino]- (m, 2 H), 5.25 (ddd, J = 25, 9, 4 Hz, 1 H), 2,3-dihydro-1H-inden-5-yl]acrylamide 5.48 (dt, J = 55, 4 Hz, 1 H), 5.73 (dd, J = 10, 2 Hz, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 6.79 (d, J = 10 Hz, 1 H), 7.01 (d, J = 9 Hz, 2 H), 7.28 (d, J = 8 Hz, 1 H), 7.44 (d, J = 9 Hz, 2 H), 7.59 (s, 1 H), 7.66 (d, J = 8 Hz, 1 H), 10.13 (s, 1 H) 91 N-(2-fluoro-3-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 3.09 [M + H]+ 556 1.09 A (trifluoromethyl)phenyl)amino)- (m, 1 H), 3.23 (m, 1 H), 5.26 (ddd, J = 25, 10, 2,3-dihydro-1H-inden-5-yl)acrylamide 4 Hz, 1 H), 5.46 (dt, J = 55, 4 Hz, 1 H), 5.72 (dd, J = 10, 2 Hz, 1 H), 6.22 (dd, J = 17, 2 Hz, 1 H), 6.41 (dd, J = 17, 10 Hz, 1 H), 6.56 (d, J = 10 Hz, 1 H), 6.88 (d, J = 8 Hz, 1 H), 7.15 (d, J = 8 Hz, 1 H), 7.19 (s, 1 H), 7.26 (d, J = 8 Hz, 1 H), 7.33 (t, J = 8 Hz, 1 H), 7.60 (s, 1 H), 7.64 (d, J = 8 Hz, 1 H), 10.11 (s, 1 H) 92 N-[2-fluoro-3-[4- 1H NMR (400 MHz, DMSO-d6) δ ppm 3.06 [M + H]+ 366 1.41 A (trifluoromethyl)phenoxy]- (m, 2 H), 5.45 (m, 1 H), 5.73 (dd, J = 10, 2 2,3-dihydro-1H-inden-5-yl]acrylamide Hz, 1 H), 6.12 (m, 1 H), 6.23 (dd, J = 17, 2 Hz, 1 H), 6.39 (dd, J = 17, 10 Hz, 1 H), 7.31 (dd, J = 8, 4 Hz, 3 H), 7.66 (m, 1 H), 7.74 (m, 3 H), 10.16 (s, 1 H) 93 N-methyl-N-(2-methyl-1-((3- 1H NMR (400 MHz, DMSO-d6) δ ppm 0.81 [M + H]+ 375 1.55 A (trifluoromethyl)phenyl)amino)- (d, J = 7 Hz, 3 H), 2.64 (dd, J = 16, 4 Hz, 1 H), 2,3-dihydro-1H-inden-5-yl)acrylamide 2.92 (ddt, J = 10, 7, 4, 4 Hz, 1 H), 3.08 (dd, J = 16, 7 Hz, 1 H), 3.24 (s, 3 H), 5.10 (dd, J = 9, 7 Hz, 1 H), 5.58 (m, 1 H), 6.07 (m, 1 H), 6.14 (d, J = 3 Hz, 1 H), 6.44 (d, J = 9 Hz, 1 H), 6.84 (d, J = 8 Hz, 1 H), 7.08 (m, 2 H), 7.11 (dd, J = 8, 2 Hz, 1 H), 7.20 (d, J = 2 Hz, 1 H), 7.31 (br t, J = 8 Hz, 1 H), 7.36 (d, J = 8 Hz, 1 H) 94 N-[(cis)-3-methoxy-1-[3- 1H NMR (400 MHz, DMSO-d6) δ = 10.19 (s, [M+Na]+ 399 0.95 C (trifluoromethyl)anilino]- 1H, CONH), 7.84 (s, 1H, Ar), 7.52 (dd, J = 2,3-dihydro-1H-inden-5-yl]acrylamide 1.6, 8.4 Hz, 1H, Ar), 7.33-7.27 (m, 1H, Ar), 7.23 (d, J = 8.0 Hz, 1H, Ar), 7.00 (s, 1H, ArNH), 7.00-6.95 (m, 1H, Ar), 6.84 (d, J = 7.6 Hz, 1H, Ar), 6.51 (d, J = 8.4 Hz, 1H, Ar), 6.48-6.38 (m, 1H, CH2CH), 6.31-6.21 (m, 1H, CHCH2), 5.75 (dd, J = 2.0, 10.0 Hz, 1H, CHCH2), 4.89 (q, J = 7.6 Hz, 1H, CH), 4.77 (t, J = 6.8 Hz, 1H, CH), 3.39 (s, 3H, CH3), 3.01 (td, J = 6.8, 12.4 Hz, 1H, CH2), 1.63 (td, J = 7.6, 12.4 Hz, 1H, CH2). 95 N-[(trans)-2-hydroxy-1-[3- 1H NMR (400 MHz, DMSO-d6) δ = 10.11 (s, [M+Na]+ 385 0.86 C (trifluoromethyl)anilino]- 1H, CONH), 7.64 (s, 1H, Ar), 7.40 (dd, J = 2,3-dihydro-1H-inden-5-yl]acrylamide 1.6, 8.4 Hz, 1H, Ar), 7.29 (t, J = 8.0 Hz, 1 H, Ar), 7.18 (d, J = 8.0 Hz, 1 H, Ar), 7.02-7.00 (m, 2H, Ar), 6.82 (d, J = 7.6 Hz, 1H, Ar), 6.47-6.38 (m, 2H, CHCH2, NH), 6.27-6.22 (m, 1H, CHCH2), 5.74 (dd, J = 2.0, 10.0 Hz, 1H, CHCH2), 5.34 (d, J = 4.8 Hz, 1H, OH), 4.62-5.91 (m, 1H, CH), 4.21-4.16 (m, 1H, CH), 3.17 (dd, J = 6.8, 16.4 Hz, 1H, CH2), 2.72 (dd, J = 5.6, 16.0 Hz, 1H, CH2) 96 N-[rac-(2R,3R)-2-hydroxy-3-[3- 1H NMR (400 MHz, DMSO-d6) δ = 10.07 (s, [M + H]+ 363 0.86 C (trifluoromethyl)anilino]- 1H, CONH), 7.60 (dd, J = 1.2, 8.0 Hz, 1 H, 2,3-dihydro-1H-inden-5-yl]acrylamide Ar), 7.50 (s, 1H, Ar), 7.30 (t, J = 8.0 Hz, 1H, Ar), 7.18 (d, J = 8.4 Hz, 1H, Ar), 7.02-7.00 (m, 2H, Ar), 6.83 (d, J = 7.6 Hz, 1H, Ar), 6.49 (d, J = 8.0 Hz, 1 H, NH), 6.39 (dd, J = 10.0, 17.2 Hz, 1H, CHCH2), 6.21 (dd, J = 1.6, 16.8 Hz, 1H, CHCH2), 5.71 (dd, J = 2.0, 10.0 Hz, 1H, CHCH2), 5.36 (d, J = 5.2 Hz, 1H, OH), 4.68-4.65 (m, 1H, CH), 4.22- 4.18 (m, 1H, CH), 3.11 (dd, J = 6.8, 15.6 Hz, 1H, CH2), 2.69 (dd, J = 6.0, 15.6 Hz, 1H, CH2)

[0559] TEAD-Luciferase Reporter Assay

[0560] Luciferase-based gene reporter assays were used, employing the TEAD responsive promoter element that are stably integrated to different human tumor cell lines in order to monitor YAP1-TEAD and TAZ-TEAD activity and to study YAP1/TAZ-TEAD activity modulation by small molecule compounds. Luciferase-based gene reporter assays employing the GAPDH promoter element and stably integrated to different human tumor cell lines are used as counter screen control cell lines.

[0561] Tumor cell lines with stable integration of the 8XGTIIC-Luciferase construct (Dupont et al., Nature 2011) or the GAPDH-Luciferase control plasmid, are seeded in culture medium in 96-well plates at a density of 8000 cells/well. Following an overnight incubation in a 37° C., 5% CO2 growth chamber, cells are treated with compounds described above at 10 doses ranging between 1 and 10000 nM for 48 hrs. After compound incubation, cells are lysed with Bright-Glo Luciferase Assay System (Promega E2620) and luciferase activity is measured using a luminescent plate reader.

[0562] The inhibitory activity of the compounds with respect to luciferase activity is given by the concentration which inhibits 50% of activity of non-treated cells. IC50s are determined with a nonlinear regression model on XLfit software analysis (IDBS, UK).

[0563] The IC50 values for the compounds of the invention were generally less than 1 μM, more particularly between 1 and 550 nM and even more particularly between 1 and 100 nM, as indicated in the table below:

TABLE-US-00002 example No TEAD IC50 (nM) 1 72 2 38 3 109 4 142 5 29 6 31 7 28 8 132 9 167 10 44 11 37 12 55 13 37 14 54 15 48 16 38 17 >10000 18 213 19 503 20 358 21 262 22 >10000 23 9527 24 8040 25 8236 26 >10000 27 >10000 28 4021 29 >10000 30 >10000 31 20 32 64 33 170 34 2526 35 583 36 99 37 24 38 74 39 53 40 15 41 87 42 29 43 140 44 38 45 12 46 4564 47 4347 48 69 49 105 50 76 51 4334 52 2822 53 57 54 388 55 38 56 44 57 134 58 216 59 60 60 346 61 178 62 70 63 144 64 806 65 1849 66 863 67 53 68 290 69 349 70 5259 71 820 72 861 73 1313 74 3687 75 4717 76 777 77 56 78 52 79 8670 80 300 81 117 82 31 83 109 84 153 85 42 86 134 87 28 88 51 89 1056 90 84 91 209 92 95 93 513 94 395 95 653 96 1977

[0564] It is therefore apparent that the compounds of formula (I), in particular of formula (I′), have an inhibitory activity of YAP1/TAZ-TEAD or TEAD-dependent gene transcription.

[0565] The compounds of formula (I), in particular of formula (I′), may thus be used as inhibitors of YAP1/TAZ-TEAD or TEAD-dependent gene transcription.

[0566] The compounds of formula (I), in particular of formula (I′), may thus be used as medicaments, especially medicaments which are inhibitors of YAP1/TAZ-TEAD or TEAD-dependent gene transcription.

[0567] Thus, according to another of its aspects, a subject of the invention is medicaments that comprise a compound of formula (I), in particular of formula (I′), or an addition salt thereof with a pharmaceutically acceptable acid.

[0568] These medicaments are employed therapeutically in the treatment of cancer, in particular in the treatment of breast, ovarian, uterine, prostate, lung, gastric, colorectal, bladder, pancreatic and liver cancers, sarcomas, esophageal, head and neck cancers, uveal melanoma, or glioma.

[0569] According to another of its aspects, the present invention relates to pharmaceutical compositions comprising as active principle, a compound of formula (I), in particular of formula (I′). These pharmaceutical compositions contain an effective dose of at least one compound of formula (I), in particular of formula (I′), or a pharmaceutically acceptable salt of the said compound.

[0570] These pharmaceutical compositions may also contain at least one pharmaceutically acceptable excipient.

[0571] The said excipients are chosen, according to the pharmaceutical form and the desired mode of administration, from the usual excipients known to those skilled in the art.

[0572] The compounds of formula (I), in particular of formula (I′), may be used in the treatment of pathologies involving YAP1/TAZ-TEAD or TEAD-dependent gene transcription inhibitors.

[0573] In particular, the compounds of formula (I), in particular of formula (I′), may be used as an anticancer agent, in particular for use in the treatment of breast, ovarian, uterine, prostate, lung, gastric, colorectal, bladder, pancreatic and liver cancers, sarcomas, esophageal, head and neck cancers, uveal melanoma, or glioma.

[0574] The compounds of formula (I), in particular of formula (I′), may also be used in the treatment of a patient who has exhibited resistance to prior anti-cancer therapy.

[0575] The present invention, according to another of its aspects, also provides a method of treating the pathologies indicated above.

[0576] Thus, described is also a method of treating cancer, in particular breast, ovarian, uterine, prostate, lung, gastric, colorectal, bladder, pancreatic and liver cancers, sarcomas, esophageal, head and neck cancers, uveal melanoma, or glioma, including administering to a subject in need thereof a therapeutically effective amount of at least one compound of formula (I), in particular of formula (I′), or a pharmaceutically acceptable salt thereof.

[0577] The compounds of formula (I), in particular of formula (I′), may also be used in a method if treating cancer in a patient who has exhibited resistance to prior anti-cancer therapy.

[0578] These compounds may be used in monotherapy or combination with radiotherapy or chemotherapy.