IP Library Granted Patent US 9,127,003
Granted Patent B2
US 9,127,003 · App. 14/416,937 · Granted Sep 8, 2015

2-(azaindol-2-yl)benzimidazoles as PAD4 inhibitors

Inventors: Stephen John Atkinson (Stevenage, GB); Michael David Barker (Stevenage, GB); Matthew Campbell (Stevenage, GB); Hawa Diallo (Stevenage, GB); Clement Douault (Stevenage, GB); Neil Stuart Garton (Stevenage, GB); John Liddle (Stevenage, GB); Robert John Sheppard (Stevenage, GB); Ann Louise Walker (Stevenage, GB); Christopher Wellaway (Stevenage, GB); David Matthew Wilson (Stevenage, GB)
Assignee: Glaxo Group Limited
C07D471/04A61K31/407A61K31/4184
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Quick Facts
Patent No.
US 9,127,003
App. No.
14/416,937
Granted
Sep 8, 2015
Kind
B2
Abstract

Compounds of formula (I): wherein; R 1 is hydrogen or C 1-6 alkyl; R 2 is hydrogen, C 1-6 alkyl, perhalomethylC 0-5 alkyl-O—, or C 1-6 alkoxy; R 3 is hydrogen, C 1-6 alkyl, or C 1-6 alkoxyC 1-6 alkyl; R 4 is hydrogen, C 1-6 alkyl, perhalomethylC 1-6 alkyl; or unsubstituted C 3-6 cycloalkylC 1-6 alkyl; A is C—R 5 or N; B is C—R 6 or N; D is C—R 7 or N; with the proviso that at least one of A, B, and D, is N; R 5 is hydrogen or C 1-6 alkyl; R 6 is hydrogen or C 1-6 alkyl; R 7 is hydrogen, C 1-6 alkyl, C 1-6 alkoxy, or hydroxy; R 8 is hydrogen or C 1-6 alkyl, with the proviso that one of R 4 and R 8 is hydrogen; R 9 is hydrogen or hydroxy; R 10 is hydrogen or C 1-6 alkyl; and salts thereof are PAD4 inhibitors and may be useful in the treatment of various disorders, for example rheumatoid arthritis, vasculitis, systemic lupus erythematosus, ulcerative colitis, cancer, cystic fibrosis, asthma, cutaneous lupus erythematosis, and psoriasis.

Claims (53)

1. A compound of formula (I):

wherein;

R 1 is hydrogen or C 1-6 alkyl;

R 2 is hydrogen, C 1-6 alkyl, perhalomethylC 0-5 alkyl-O—, or C 1-6 alkoxy;

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

R 4 is hydrogen, C 1-6 alkyl, perhalomethylC 1-6 alkyl; or unsubstituted C 3-6 cycloalkylC 1-6 alkyl;

A is C—R 5 or N;

B is C—R 6 or N;

D is C—R 7 or N;

with the proviso that at least one of A, B, and D, is N;

R 5 is hydrogen or C 1-6 alkyl;

R 6 is hydrogen or C 1-6 alkyl;

R 7 is hydrogen, C 1-6 alkyl, C 1-6 alkoxy, or hydroxy;

R 8 is hydrogen or C 1-6 alkyl, with the proviso that one of R 4 and R 8 is hydrogen;

R 9 is hydrogen or hydroxy;

R 10 is hydrogen or C 1-6 alkyl;

or a salt thereof.

2. A compound of formula (I) or a salt thereof according to claim 1 wherein R 1 is hydrogen.

3. A compound of formula (I) or a salt thereof according to claim 1 wherein R 2 is hydrogen or C 1-6 alkoxy.

4. A compound of formula (I) or a salt thereof according to claim 1 wherein R 3 is C 1-6 alkyl.

5. A compound of formula (I) or a salt thereof according to claim 1 wherein R 4 is C 1-6 alkyl, unsubstituted C 3-6 cycloalkylC 1-6 alkyl, or perhalomethylC 1-6 alkyl.

6. A compound of formula (I) or a salt thereof according to claim 1 wherein R 6 is hydrogen.

7. A compound of formula (I) or a salt thereof according to claim 1 wherein R 7 is hydrogen.

8. A compound of formula (I) or a salt thereof according to claim 1 wherein R 8 is hydrogen.

9. A compound of formula (I) or a salt thereof according to claim 1 wherein R 9 is hydrogen.

10. A compound of formula (I) or a salt thereof according to claim 1 wherein R 10 is hydrogen.

11. A compound of formula (I) or a salt thereof selected from the list consisting of:

1-{[2-(1-ethyl-1H-pyrrolo[3,2-c]pyridin-2-yl)-1-methyl-1H-benzimidazol-5-yl]carbonyl}-3-piperidinamine;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo [d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-c]pyridin-2-yl)-1-methyl-1H-benzo [d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(1-methyl-2-(1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-5-methoxy-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-5-methoxy-1H-pyrrolo[2,3-c]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

2-(5-{[(3R)-3-amino-1-piperidinyl]carbonyl}-1-methyl-1H-benzimidazol-2-yl)-1-ethyl-1H-pyrrolo[2,3-b]pyridin-5-ol;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(7-methoxy-1-methyl-2-(1-(2,2,2-trifluoroethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-benzo[d]imidazol-5-yl)methanone;

(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

((3S,4R)-3-amino-4-hydroxypiperidin-1-yl)(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

((3S,4R)-3-amino-4-hydroxypiperidin-1-yl)(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-7-(trifluoromethoxy)-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(7-methoxy-1-methyl-2-(1-neopentyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-benzo[d]imidazol-5-yl)methanone;

((R)-3-aminopiperidin-1-yl)(7-methoxy-1-methyl-2-(1-(2-methylbutyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-(2-methoxyethyl)-1H-benzo[d]imidazol-5-yl)methanone;

(S)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-ethyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-isobutyl-7-methoxy-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(7-methoxy-2-(1-(2-methoxy-2-methylpropyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-1-methyl-1H-benzo[d]imidazol-5-yl)methanone;

(R)-(3-aminopiperidin-1-yl)(2-(1-isobutyl-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone, and;

((cis)-5-amino-2-methylpiperidin-1-yl)(2-(1-(cyclopropylmethyl)-1H-pyrrolo[2,3-b]pyridin-2-yl)-7-methoxy-1-methyl-1H-benzo[d]imidazol-5-yl)methanone, and salts thereof.

12. A compound of formula (I) according to claim 1 as a pharmaceutically acceptable salt.

13. A pharmaceutical composition comprising a compound of formula (I) as defined in claim 1 , or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.

14. A method of treatment of rheumatoid arthritis, vasculitis, or systemic lupus erythematosis, which method comprises administering to a human subject in need thereof, a therapeutically effective amount of a compound of formula (I) as defined in claim 1 , or a pharmaceutically acceptable salt thereof.

Assignments (2)
CHANGE OF ADDRESS Recorded Apr 16, 2025
From: GLAXO GROUP LIMITED
To: GLAXO GROUP LIMITED
Reel/Frame 071044/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2015
From: ATKINSON, STEPHEN JOHN; BARKER, MICHAEL DAVID; CAMPBELL, MATTHEW; DIALLO, HAWA; DOUAULT, CLEMENT; GARTON, NEIL STUART; LIDDLE, JOHN; SHEPPARD, ROBERT JOHN; WALKER, ANN LOUISE; WELLAWAY, CHRISTOPHER; WILSON, DAVID MATTHEW
To: GLAXO GROUP LIMITED
Reel/Frame 034910/0248 →
Continuity (1)
Related Publication 20150175600A1 · Jun 25, 2015