IP Library Granted Patent US 12702658
Granted Patent B2
US 12702658 · App. 17/920,870 · Granted Aug 11, 2026

Anticancer combination therapy with N-(1-acryloyl-azetidin-3-yl)-2-((1H-indazol-3-yl)amino)methyl)-1H-imidazole-5-carboxamide inhibitor of KRAS-G12C

Inventors: Tetsuya Abe (Tsukuba, JP); Yoko Nakatsuru (Tsukuba, JP); Hiroshi Sootome (Tsukuba, JP)
Assignees: TAIHO PHARMACEUTICAL CO., LTD.; ASTEX THERAPEUTICS LTD.
A61K31/4178A61K31/166A61K31/416A61K31/422A61K31/427A61K31/4439A61K31/454A61K31/496A61K31/506A61K31/5365A61N5/10A61P1/00A61P1/18A61P11/00A61P13/10A61P35/00
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Quick Facts
Patent No.
US 12702658
App. No.
17/920,870
Granted
Aug 11, 2026
Kind
B2
Abstract

A method of treating cancer comprises administering: (a) a therapeutically effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof; and (b) a therapeutically effective amount of an additional anti-cancer agent, to a subject in need of such treatment, the compound of Formula (I) being: where X, R 1 , R 2 , ring A, L 1 , L 2 , L 3 , and R 5 are as defined in this disclosure.

Claims (124)

1 . A method of treating cancer comprising administering:

(a) a compound of Formula (I) or a pharmaceutically acceptable salt thereof; and

(b) an additional anti-cancer agent,

to a subject in need of such treatment, the compound of Formula (I) being:

wherein

X is nitrogen or CH,

R 1 is selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, substituted or unsubstituted C 2 -C 6 alkynyl, substituted or unsubstituted C 4 -C 10 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

R 2 is selected from the group consisting of hydrogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, substituted or unsubstituted C 2 -C 6 alkynyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

L 1 is —NH—C(R a ) 2 —, wherein R a s are identical or different, and each is a hydrogen atom, a deuterium atom, or C 1 -C 6 alkyl,

ring A is a substituted or unsubstituted 5-membered unsaturated heterocyclic group,

one of A 1 , A 2 , and A 3 is substituted or unsubstituted nitrogen or sulfur, and the rest of A 1 , A 2 , and A 3 are identical or different, and are substituted or unsubstituted carbon, substituted or unsubstituted nitrogen, sulfur, or oxygen,

when A 1 is substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl that may be substituted with R b , C 2 -C 6 alkenyl that may be substituted with R b , C 2 -C 6 alkynyl that may be substituted with R b , C 3 -C 10 cycloalkyl that may be substituted with R c , C 4 -C 10 cycloalkenyl that may be substituted with R c , C 6 -C 10 aromatic hydrocarbon that may be substituted with R c , a 4- to 10-membered saturated heterocyclic group that may be substituted with R c , and a 5- to 10-membered unsaturated heterocyclic group that may be substituted with R c ,

R b is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkoxy, C 1 -C 6 alkylamino, C 3 -C 6 cycloalkyl, substituted or unsubstituted C 6 -C 10 aromatic hydrocarbon, and a substituted or unsubstituted 5- to 10-membered saturated heterocyclic group,

R c is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 alkylamino, C 1 -C 6 alkylcarbonyl, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, C 7 -C 20 aralkyl, C 1 -C 6 alkoxycarbonyl, C 3 -C 6 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

when two or more R b s are present, the plurality of R b s may be identical or different,

when two or more R c s are present, the plurality of R c s may be identical or different,

when A 2 is substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, and substituted or unsubstituted C 2 -C 6 alkynyl,

when A 3 represents substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, and substituted or unsubstituted C 2 -C 6 alkynyl,

L 2 is

 is a 4- to 8-membered saturated heterocyclic group that contains at least one nitrogen atom, and that may contain 1 or 2 heteroatoms selected from sulfur and oxygen, in which N represents nitrogen,

R 3 is hydrogen or C 1 -C 6 alkyl,

R 4 is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 alkylamino-C 1 -C 6 alkyl, cyano-C 1 -C 6 alkyl, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, and C 1 -C 6 hydroxyalkyl,

when two or more R 4 s are present, the plurality of R 4 s may be identical or different,

when two R 4 s are attached to the same carbon atom, and these two R 4 s each represent C 1 -C 6 alkyl, then these two R 4 s, taken together with the carbon atom to which these two R 4 s are attached, may form a ring, and

n is 0, 1, 2, or 3,

L 3 is —C(—O)— or —S(═O) 2 —, and

R 5 is substituted or unsubstituted C 2 -C 6 alkenyl or substituted or unsubstituted C 2 -C 6 alkynyl.

2 . The method according to claim 1 , wherein the compound of Formula (I) is selected from the group consisting of:

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1,4-dimethyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1-isopropyl-4-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-(difluoromethyl)-1-isopropyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-isopropyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1,4-dimethyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-fluoro-1-methyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-((3R,4R)-1-acryloyl-4-methylpyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-(difluoromethyl)-1-(1-isopropylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(S)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydrofuran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydrofuran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-methylpiperidin-4-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydro-2H-pyran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-cyclopentyl-1H-imidazole-5-carboxamide;

tert-butyl 3-(5-((1-acryloylazetidin-3-yl) carbamoyl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1H-imidazol-1-yl) azetidine-1-carboxylate;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-isopropylazetidin-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(4-methoxycyclohexyl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(2,2-difluoroethyl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-isopropylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(S)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(2,2-difluoroethyl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-1-(1-allylpyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(pyridin-2-yl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-((3R,5R)-1-(2,2-difluoroethyl)-5-methylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide; and

the pharmaceutically acceptable salts thereof.

3 . The method according to claim 1 , wherein the additional anti-cancer agent is selected from the group consisting of a chemotherapeutic agent, an immunotherapeutic agent, a hormonal agent, an anti-hormonal agent, a targeted therapy agent, or an anti-angiogenesis agent.

4 . The method according to claim 1 , wherein the additional anti-cancer agent is selected from the group consisting of a MEK inhibitor, an ERK inhibitor, an AKT inhibitor, and an SHP2 inhibitor.

5 . The method according to claim 2 , wherein the additional anti-cancer agent is selected from the group consisting of a MEK inhibitor, an ERK inhibitor, an AKT inhibitor, and an SHP2 inhibitor.

6 . The method according to claim 1 , wherein the compound of Formula (I) or the pharmaceutically acceptable salt thereof is administered in a therapeutically effective amount.

7 . The method according to claim 1 , wherein the additional anti-cancer agent is administered in a therapeutically effective amount.

8 . The method according to claim 1 , wherein (a) and (b) are administered simultaneously.

9 . The method according to claim 8 , wherein (a) and (b) are administered via a single pharmaceutical preparation further comprising at least one pharmaceutical acceptable carrier.

10 . The method according to claim 1 , wherein (a) and (b) are administered separately.

11 . The method according to claim 1 , wherein (a) and (b) are administered sequentially.

12 . The method according to claim 11 , wherein (a) is administered and then (b) is administered.

13 . The method according to claim 11 , wherein (b) is administered and then (a) is administered.

14 . The method according to claim 1 , wherein the subject is a human.

15 . The method according to claim 1 , wherein the cancer is selected from the group consisting of glandular tumors, carcinoid tumors, undifferentiated carcinomas, angiosarcoma, adenocarcinoma, gastrointestinal cancers, lung cancers, urological cancers, head and neck cancers, endocrine cancers, breast cancers, male and female reproductive cancers, brain and nervous system cancers, skin cancers, tissue and bone cancers, cardiovascular cancers, appendix cancers, childhood and adolescent cancers, viral-induced cancers, multiple myeloma, leukemias, lymphomas, myelodysplastic syndromes and myeloproliferative disorders.

16 . A method of treating cancer comprising administering:

a compound of Formula (I) or a pharmaceutically acceptable salt thereof; and

radiation therapy,

to a subject in need of such treatment, the compound of Formula (I) being:

wherein

X is nitrogen or CH,

R 1 is selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, substituted or unsubstituted C 2 -C 6 alkynyl, substituted or unsubstituted C 4 -C 10 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

R 2 is selected from the group consisting of hydrogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, substituted or unsubstituted C 2 -C 6 alkynyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

L 1 is —NH—C(R a ) 2 —, wherein R a s are identical or different, and each is a hydrogen atom, a deuterium atom, or C 1 -C 6 alkyl,

ring A is a substituted or unsubstituted 5-membered unsaturated heterocyclic group,

one of A 1 , A 2 , and A 3 is substituted or unsubstituted nitrogen or sulfur, and the rest of A 1 , A 2 , and A 3 are identical or different, and are substituted or unsubstituted carbon, substituted or unsubstituted nitrogen, sulfur, or oxygen,

when A 1 is substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl that may be substituted with R b , C 2 -C 6 alkenyl that may be substituted with R b , C 2 -C 6 alkynyl that may be substituted with R b , C 3 -C 10 cycloalkyl that may be substituted with R c , C 4 -C 10 cycloalkenyl that may be substituted with R c , C 6 -C 10 aromatic hydrocarbon that may be substituted with R c , a 4- to 10-membered saturated heterocyclic group that may be substituted with R c , and a 5- to 10-membered unsaturated heterocyclic group that may be substituted with R c ,

R b is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkoxy, C 1 -C 6 alkylamino, C 3 -C 6 cycloalkyl, substituted or unsubstituted C 6 -C 10 aromatic hydrocarbon, and a substituted or unsubstituted 5- to 10-membered saturated heterocyclic group,

R c is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 alkylamino, C 1 -C 6 alkylcarbonyl, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, C 7 -C 20 aralkyl, C 1 -C 6 alkoxycarbonyl, C 3 -C 6 cycloalkyl, C 6 -C 10 aromatic hydrocarbon, a 5- to 10-membered saturated heterocyclic group, and a 5- to 10-membered unsaturated heterocyclic group,

when two or more R b s are present, the plurality of R b s may be identical or different,

when two or more R c s are present, the plurality of R c s may be identical or different,

when A 2 is substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, and substituted or unsubstituted C 2 -C 6 alkynyl,

when A 3 represents substituted carbon or substituted nitrogen, the substituent is at least one member selected from the group consisting of hydrogen, halogen, cyano, nitro, amino, hydroxy, carboxy, substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 2 -C 6 alkenyl, and substituted or unsubstituted C 2 -C 6 alkynyl,

L 2 is

 is a 4- to 8-membered saturated heterocyclic group that contains at least one nitrogen atom, and that may contain 1 or 2 heteroatoms selected from sulfur and oxygen, in which N represents nitrogen,

R 3 is hydrogen or C 1 -C 6 alkyl,

R 4 is selected from the group consisting of halogen, cyano, nitro, amino, hydroxy, carboxy, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl, C 1 -C 6 alkylamino-C 1 -C 6 alkyl, cyano-C 1 -C 6 alkyl, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, and C 1 -C 6 hydroxyalkyl,

when two or more R 4 s are present, the plurality of R 4 s may be identical or different,

when two R 4 s are attached to the same carbon atom, and these two R 4 s each represent C 1 -C 6 alkyl, then these two R 4 s, taken together with the carbon atom to which these two R 4 s are attached, may form a ring, and

n is 0, 1, 2, or 3,

L 3 is —C(═O)— or —S(═O) 2 —, and

R 5 is substituted or unsubstituted C 2 -C 6 alkenyl or substituted or unsubstituted C 2 -C 6 alkynyl.

17 . The method according to claim 16 , wherein the compound of Formula (I) is selected from the group consisting of:

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1,4-dimethyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1-isopropyl-4-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-(difluoromethyl)-1-isopropyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-isopropyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-1,4-dimethyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-fluoro-1-methyl-1H-imidazole-5-carboxamide;

N-((3S,4S)-1-acryloyl-4-fluoropyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-((3R,4R)-1-acryloyl-4-methylpyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-methyl-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-(difluoromethyl)-1-(1-isopropylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(S)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydrofuran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydro-2H-pyran-4-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydrofuran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-methylpiperidin-4-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(tetrahydro-2H-pyran-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-cyclopentyl-1H-imidazole-5-carboxamide;

tert-butyl 3-(5-((1-acryloylazetidin-3-yl) carbamoyl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1H-imidazol-1-yl) azetidine-1-carboxylate;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-isopropylazetidin-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(4-methoxycyclohexyl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(2,2-difluoroethyl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-isopropylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(S)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(2,2-difluoroethyl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-1-(1-allylpyrrolidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1H-imidazole-5-carboxamide;

(R)-N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-(1-(pyridin-2-yl) pyrrolidin-3-yl)-1H-imidazole-5-carboxamide;

N-(1-acryloylazetidin-3-yl)-2-(((5-(tert-butyl)-6-chloro-1H-indazol-3-yl)amino)methyl)-4-chloro-1-((3R,5R)-1-(2,2-difluoroethyl)-5-methylpyrrolidin-3-yl)-1H-imidazole-5-carboxamide; and

the pharmaceutically acceptable salts thereof.

18 . The method according to claim 16 , wherein the compound of Formula (I) or the pharmaceutically acceptable salt thereof is administered in a therapeutically effective amount.

19 . The method according to claim 16 , wherein the subject is a human.

20 . The method according to claim 16 , wherein the cancer is selected from the group consisting of glandular tumors, carcinoid tumors, undifferentiated carcinomas, angiosarcoma, adenocarcinoma, gastrointestinal cancers, lung cancers, urological cancers, head and neck cancers, endocrine cancers, breast cancers, male and female reproductive cancers, brain and nervous system cancers, skin cancers, tissue and bone cancers, cardiovascular cancers, appendix cancers, childhood and adolescent cancers, viral-induced cancers, multiple myeloma, leukemias, lymphomas, myelodysplastic syndromes and myeloproliferative disorders.