IP Library › Granted Patent US 9,586,965
Granted Patent B2
US 9,586,965 · App. 14/420,341 · Granted Mar 7, 2017

Pyrrolo[2,3-d]pyrimidine compounds as inhibitors of protein kinases

Inventors: Xiao Xu (San Diego, CA); Xiaobo Wang (San Diego, CA); Long Mao (San Diego, CA); Li Zhao (San Diego, CA); Biao Xi (San Diego, CA)
Assignee: ACEA BIOSCIENCES INC.
C07D487/04A61K31/519A61K45/06
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Quick Facts
Patent No.
US 9,586,965
App. No.
14/420,341
Granted
Mar 7, 2017
Kind
B2
Abstract

The present invention relates to certain pyrrolopyrimidine derivatives, pharmaceutical compositions containing them, and methods of using them, including methods for the treatment of proliferation disorders and other diseases related to the dysregulation of kinase (such as, but not limited to, EGFR (including HER), Alk, PDGFR, BLK, BMX/ETK, BTK, FLT3(D835Y), ITK, JAK1, JAK2, JAK3, TEC and TXK) and/or the respective pathways.

Claims (62)

1. A compound of Formula (VII):

wherein

R 1 and R 2 are independently selected from hydrogen, halo, C 1-6 alkyl, and C 1-6 haloalkyl;

R 8 is selected from halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 10 is C 1-6 alkyl; and

R 13 is hydrogen or C 1-6 alkyl;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , wherein R 1 and R 2 are each hydrogen.

3. The compound of claim 1 , wherein R 8 is halo.

4. The compound of claim 3 , wherein R 8 is fluoro.

5. The compound of claim 1 , wherein R 10 is methyl, ethyl, or isopropyl.

6. The compound of claim 5 , wherein R 10 is methyl.

7. The compound of claim 1 , wherein R 13 is hydrogen.

8. A compound of Formula (III):

wherein

R 1 and R 2 are independently selected from hydrogen, halo, C 1-6 alkyl, and C 1-6 haloalkyl;

R 3 is selected from halo, hydroxyl, C 1-6 alkyl, C 1-6 alkoxy, cyano, and nitro;

n is a number from zero to 4;

R 4 is selected from hydrogen, C 1-6 alkyl, C 3-7 cycloalkyl, and NR 22 R 23 ;

wherein the alkyl or cycloalkyl is unsubstituted or substituted with hydroxyl or amino; and

wherein each R 22 and R 23 is independently selected from hydrogen and C 1-6 alkyl, or R 22 and R 23 taken with the nitrogen to which they are attached are joined to form a 3 to 10 membered ring;

R 5 is selected from hydrogen and C 1-6 alkyl;

R 6 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 7 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 8 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 9 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 10 is selected from hydrogen and C 1-6 alkyl;

R 11 is selected from hydrogen and C 1-6 alkyl;

R 12 is selected from hydrogen and C 1-6 alkyl; and

R 13 is selected from hydrogen, C 1-6 alkyl, and C 6-20 aryl, wherein each alkyl or aryl is unsubstituted or substituted with hydroxyl, C 1-6 alkoxy, or halo;

or a pharmaceutically acceptable salt thereof.

9. The compound of claim 8 , wherein R 11 and R 12 are each hydrogen.

10. The compound of claim 8 , wherein R 1 and R 2 are each hydrogen.

11. The compound of claim 8 , wherein n is zero.

12. The compound of claim 8 , wherein R 10 is methyl.

13. The compound of claim 8 , wherein R 13 is hydrogen.

14. The compound of claim 8 , wherein R 9 is hydrogen or halo.

15. The compound of claim 14 , wherein R 9 is fluoro.

16. The compound of claim 8 , wherein R 6 and R 7 are hydrogen.

17. The compound of claim 8 , wherein R 8 is hydrogen or halo.

18. The compound of claim 8 , wherein R 6 , R 7 , and R 8 are hydrogen and R 9 is fluoro.

19. The compound of claim 8 , wherein R 4 and R 5 are each hydrogen.

20. A pharmaceutical composition comprising: (a) at least one compound of claim 8 or a pharmaceutically acceptable salt thereof; and (b) a pharmaceutically acceptable carrier or excipient.

21. The pharmaceutical composition of claim 20 , wherein the pharmaceutically acceptable salt is an HCl salt, a maleate salt, an HBr salt, a hydroxybutanedioic acid salt, or a fumaric acid salt.

22. A compound of Formula (VI):

wherein

R 1 and R 2 are independently selected from hydrogen, halo, C 1-6 alkyl, and C 1-6 haloalkyl;

R 8 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

Q is CR 9 or N;

R 9 is selected from hydrogen, halo, C 1-6 alkyl, C 1-6 haloalkyl, C 1-6 haloalkoxy, hydroxyl, cyano, and nitro;

R 10 is selected from hydrogen and C 1-6 alkyl; and

R 13 is selected from hydrogen, C 1-6 alkyl, and C 6-20 aryl, wherein each alkyl or aryl is unsubstituted or substituted with hydroxyl, C 1-6 alkoxy, or halo;

or a pharmaceutically acceptable salt thereof.

23. The compound of claim 22 , wherein R 1 and R 2 are each hydrogen.

24. The compound of claim 22 , wherein Q is CR 9 .

25. The compound of claim 24 , wherein R 9 is hydrogen or halo.

26. The compound of claim 22 , wherein R 8 is hydrogen or halo.

27. The compound of claim 22 , wherein one of R 8 and R 9 is hydrogen and the other is fluoro.

28. The compound of claim 22 , wherein R 10 is methyl.

29. The compound of claim 22 , wherein R 13 is hydrogen.

30. A compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2018
From: ACEA BIOSCIENCES, INC.
To: ACEA THERAPEUTICS, INC.
Reel/Frame 047492/0140 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2015
From: XU, XIAO; WANG, XIAOBO; MAO, LONG; ZHAO, LI; XI, BIAO
To: ACEA BIOSCIENCES INC.
Reel/Frame 035906/0577 →
Continuity (5)
Continuation In Part 13843554 · Mar 15, 2013
Continuation In Part 13917514 · Jun 13, 2013
Provisional Application 61680231 · Aug 6, 2012
Provisional Application 61814147 · Apr 19, 2013
Related Publication 20150210702A1 · Jul 30, 2015