IP Library › Granted Patent US 9,688,629
Granted Patent B2
US 9,688,629 · App. 14/921,347 · Granted Jun 27, 2017

Indole carboxamide compounds

Inventors: Qingjie Liu (Newtown, PA); Scott Hunter Watterson (Pennington, NJ); Saleem Ahmad (Wall, NJ)
Assignee: Bristol-Myers Squibb Company
C07D209/08C07D209/18C07D401/04C07D401/06C07D401/12C07D403/04C07D403/10C07D403/12C07D417/04C07D471/04C07D487/04C07D487/10
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Quick Facts
Patent No.
US 9,688,629
App. No.
14/921,347
Granted
Jun 27, 2017
Kind
B2
Abstract

Disclosed are compounds of Formula (I): or a salt thereof, wherein: X is CR 4 or N; R 1 , R 2 , R 3 , R 4 , and A are defined herein. Also disclosed are methods of using such compounds as inhibitors of Bruton's tyrosine kinase (Btk), and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as autoimmune diseases and vascular disease.

Claims (38)

1. A compound of Formula (I):

or a salt thereof, wherein:

X is —CR 4 ;

R 1 is —CH 3 or —CF 3 ;

R 2 is —CH 3 or cyclopropyl;

R 3 is F, Cl, or I;

R 4 is H;

A is:

Q 2 is —CN, —C(O)CH═CH 2 , —S(O) 2 CH═CH 2 , —C(O)CH═CHCH 2 N(CH 3 ) 2 , —C(O)C≡CH, —C(O)C≡CCH 3 , —C(O)C≡CCH 2 CH 3 , —C(O) C≡CCH 2 CH 2 CH 3 , —C(O)C≡CC(CH 3 ) 2 OH, —C(O)C≡CSi(CH 3 ) 3 , —C(O)C≡C(cyclopropyl), or —C(O)C≡C(phenyl); and

R 7 is H or —CH 3 .

2. The compound according to claim 1 or a salt thereof, wherein R 3 is F or Cl.

3. The compound according to claim 1 or a salt thereof, wherein R 3 is F.

4. The compound according to claim 1 or a salt thereof, wherein:

R 1 is —CH 3 ;

R 2 is —CH 3 ;

R 3 is F;

Q 2 is —CN, —C(O) CH═CH 2 , —S(O) 2 CH═CH 2 , —C(O)C≡CH, —C(O)C≡CCH 2 CH 3 , —C(O)C≡CCH 2 CH 2 CH 3 , or —C(O)C≡C(cyclopropyl);

R 7 is H.

5. The compound according to claim 1 or a salt thereof, wherein said compound is selected from: (S)-4-(3-acrylamidopiperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide (89); (S)-5-fluoro-2,3-dimethyl-4-(3-(N-methylbut-2-ynamido)piperidin-1 -yl)-1 H -indole-7-carboxamide (125); (S)-5-fluoro-2,3-dimethyl-4-(3-(pent-2-ynamido) piperidin-1-yl)-1H -indole-7-carboxamide (126); (S)-5-fluoro-2,3-dimethyl-4-(3-(N-methylpent-2-ynamido)piperidin-1-yl)-1H-indole-7-carboxamide (127); (S)-5-fluoro-4-(3-(hex-2-ynamido)piperidin-1-yl)-2,3-dimethyl-1H-indole-7-carboxamide (128); (S)-4-(3-(3-cyclopropylpropiolamido)piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide (136); (S)-5-fluoro-2,3-dimethyl-4-(3-(vinylsulfonamido) piperidin-1-yl)-1H-indole-7-carboxamide (146); (S)-4-(3-cyanamidopiperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide (150); (S)-4-(3-(but-2-ynamido) piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide (223); (S)-5-fluoro-2,3-dimethyl-4-(3-propiolamidopiperidin-1-yl)-1H-indole-7-carboxamide (242); and (R)-4-(3-(but-2-ynamido) piperidin-1-yl)-5-fluoro-2,3-dimethyl-1H-indole-7-carboxamide (243).

6. A pharmaceutical composition comprising a compound according to claim 1 or a pharmaceutically-acceptable salt thereof; and a pharmaceutically acceptable carrier.

7. A method for treating a disease comprising the administration to a subject in need thereof a therapeutically-effective amount of at least one compound according to claim 1 or a pharmaceutically-acceptable salt thereof, wherein said disease is rheumatoid arthritis.

8. A pharmaceutical composition comprising a compound according to claim 5 or a pharmaceutically-acceptable salt thereof; and a pharmaceutically acceptable carrier.

9. A method for treating a disease comprising the administration to a subject in need thereof a therapeutically-effective amount of at least one compound according to claim 5 or a pharmaceutically-acceptable salt thereof, wherein said disease is rheumatoid arthritis.

10. A compound having the structure:

or a salt thereof.

11. The compound according to claim 10 .

12. A pharmaceutical composition comprising a compound according to claim 10 or a pharmaceutically-acceptable salt thereof; and a pharmaceutically acceptable carrier.

13. A method for treating a disease comprising administration to a subject in need thereof a therapeutically-effective amount of at least one compound according to claim 10 or a pharmaceutically-acceptable salt thereof, wherein said disease is rheumatoid arthritis.

14. A compound having the structure:

or a salt thereof.

15. The compound according to claim 14 .

16. A pharmaceutical composition comprising a compound according to claim 14 or a pharmaceutically-acceptable salt thereof; and a pharmaceutically acceptable carrier.

17. A method for treating a disease comprising the administration to a subject in need thereof a therapeutically-effective amount of at least one compound according to claim 14 or a pharmaceutically-acceptable salt thereof, wherein said disease is rheumatoid arthritis.

18. A compound having the structure:

or a salt thereof.

19. The compound according to claim 18 .

20. A pharmaceutical composition comprising a compound according to claim 18 or a pharmaceutically-acceptable salt thereof; and a pharmaceutically acceptable carrier.

21. A method for treating a disease comprising the administration to a subject in need thereof a therapeutically-effective amount of at least one compound according to claim 18 or a pharmaceutically-acceptable salt thereof, wherein said disease is rheumatoid arthritis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2018
From: AHMAD, SALEEM; TINO, JOSEPH A.; MACOR, JOHN E.; TEBBEN, ANDREW J.; GONG, HUA; LIU, QINGJIE; BATT, DOUGLAS G.; NGU, KHEHYONG; WATTERSON, SCOTT HUNTER; GUO, WEIWEI; BERTRAND, MYRA BEAUDOIN
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 046128/0452 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2016
From: AHMAD, SALEEM; TINO, JOSEPH A.; MACOR, JOHN E.; TEBBEN, ANDREW J.; GONG, HUA; LIU, QINGJIE; BATT, DOUGLAS G.; NGU, KHEHYONG; WATTERSON, SCOTT HUNTER; GUO, WEIWEI; BERTRAND, MYRA BEAUDOIN
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 038001/0396 →
Continuity (2)
Provisional Application 62068225 · Oct 24, 2014
Related Publication 20160115126A1 · Apr 28, 2016