IP Library Granted Patent US 9,290,505
Granted Patent B2
US 9,290,505 · App. 14/578,973 · Granted Mar 22, 2016

Substituted imidazo[1,2-a]pyrazines as Syk inhibitors

Inventors: Peter A. Blomgren (North Branford, CT); Kevin S. Currie (North Branford, CT); Jeffrey E. Kropf (Branford, CT); Seung H. Lee (Branford, CT); Jennifer R. Lo (Branford, CT); Scott A. Mitchell (East Haven, CT); Aaron C. Schmitt (Hamden, CT); Jin-Ming Xiong (Guilford, CT); Jianjun Xu (Madison, CT); Zhongdong Zhao (Guilford, CT); Sundaramoorthi Swaminathan (Burlingame, CA)
Assignee: Gilead Sciences, Inc.
C07D487/04
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Quick Facts
Patent No.
US 9,290,505
App. No.
14/578,973
Granted
Mar 22, 2016
Kind
B2
Abstract

The present disclosure relates to compounds that are Syk inhibitors and to their use in the treatment of various disease states, including cancer and inflammatory conditions. In particular embodiments, the structure of the compounds is given by Formula I: wherein R 1 , R 2 , R 3 , and R 4 are as described herein. The present disclosure further provides pharmaceutical compositions that include a compound of Formula I, or pharmaceutically acceptable salts or co-crystals thereof, and methods of using these compounds and compositions to treat conditions mediated by Syk.

Claims (64)

1. A compound having the structure of Formula I:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein;

R 1 is selected from the group consisting of

 wherein * indicates the carbon atom of the indicated phenyl ring of Formula I to which R 1 is attached;

R 2 is H or 2-hydroxyethoxy;

R 3 is H or methyl; and

R 4 is H or methyl.

2. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomerthereof, wherein R 1 is

3. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 1 is

4. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 1 is

5. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 1 is

6. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 2 is 2-hydroxyethoxy.

7. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 2 is H.

8. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 3 is methyl.

9. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, phaimaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof wherein R 3 is H.

10. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 4 is methyl.

11. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 4 is H.

12. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 2 is H, R 3 is methyl, and R 4 is H.

13. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein R 2 is H, R 3 is H, and R 4 is methyl.

14. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R 2 , R 3 , and R 4 is H.

15. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R 2 is 2-hydroxyethoxy, R 3 is methyl, and R 4 is H.

16. The compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, wherein each of R 2 is 2-hydroxyethoxy, R 3 is H, and R 4 is methyl.

17. The compound of claim 1 , wherein the pharmaceutically acceptable salt or co-crystal is a mesylate salt or co-crystal.

18. The compound of claim 1 , wherein the pharmaceutically acceptable salt or co-crystal is a succinate salt or co-crystal.

19. The compound according to claim 1 , selected from the group consisting of:

2-(5-))6-(6-amino-5-methylpyrazin-2-yl)imidazo [1 ,2-a]pyrazin-8-yl)amino)-2-(4-(oxetan-3-yl)piperazin-1-yl)phenoxy)ethanol;

6-(6-aminopyrazin-2-yl)-N-(4-(4- (oxetan-3-yl)piperazin-1-yl)pheny) imidazo[1,2-a]pyrazin-8-amine;

2-((4-(4-((6-(6-aminopyrazin-2-yl)imidazo[1,2-a]pyrazin-8-yl)amino)phenyl)piperazin-1-yl)methyl)propane-1,3-diol;

2- (5-((6-(6-aminopyrazin-2- yl)imidazo[1 ,2-a]pyrazin-8-yl)amino)-2-(4-(oxetan-3-yl)piperazin- 1-yl)phenoxy)ethanol;

(R)-(4- (4((6-(6-aminopyrazin-2-yl)imidazo[1 ,2- a]pyrazin-8-yl)amino)phenyl)morpholin-2-Yl)methanol;

6-(6-aminopyrazin-2-yl)-5-methyl-N-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1 ,2-A]pyrazin-8-amine; and

6-(6-amino-5-methylpyrazin-2-yl)-N-(4-(4-(oxetan-3-yl)piperazin-1-yl)phenyl)imidazo[1,2-a]pyrazin-8-amine;

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

20. The compound of claim 19 , wherein the pharmaceutically acceptable salt or co-crystal is a mesylate salt or co-crystal.

21. The compound of claim 19 , wherein the pharmaceutically acceptable salt or co-crystal is a succinate salt or co-crystal.

22. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 , or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

23. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stercoisomer, mixture of stereoisomers, or tautomer thereof.

24. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

25. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

26. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

27. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

28. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

29. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

30. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

31. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

32. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

33. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers, or tautomer thereof.

34. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

35. A compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stercoisomer, mixture of stereoisomers, or tautomer thereof.

36. A pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula:

or a pharmaceutically acceptable salt, pharmaceutically acceptable co-crystal, pharmaceutically acceptable ester, stereoisomer, mixture of stereoisomers or tautomer thereof, and at least one pharmaceutically acceptable vehicle.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2026
From: KRONOS BIO, INC.
To: IGNOTA LABS LIMITED
Reel/Frame 075588/0486 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2020
From: GILEAD SCIENCES, INC.
To: KRONOS BIO, INC.
Reel/Frame 053797/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2018
From: BLOMGREN, PETER A.; CURRIE, KEVIN S.; KROPF, JEFFREY E.; LEE, SEUNG H.; LO, JENNIFER R.; MITCHELL, SCOTT A.; SCHMITT, AARON C.; XIONG, JIN-MING; XU, JIANJUN; ZHAO, ZHONGDONG
To: GILEAD SCIENCES, INC.
Reel/Frame 046428/0906 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2015
From: SWAMINATHAN, SUNDARAMOORTHI
To: GILEAD SCIENCES, INC.
Reel/Frame 035536/0828 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 20, 2015
From: BLOMGREN, PETER A.; CURRIE, KEVIN S.; KROPF, JEFFREY E.; LEE, SEUNG H.; LO, JENNIFER R.; MITCHELL, SCOTT A.; SCHMITT, AARON C.; XIONG, JIN-MING; ZHAO, ZHONGDONG; XU, JIANJUN
To: GILEAD SCIENCES, INC.
Reel/Frame 035214/0688 →
Continuity (2)
Provisional Application 61920407 · Dec 23, 2013
Related Publication 20150175616A1 · Jun 25, 2015