IP Library › Granted Patent US 9,464,089
Granted Patent B2
US 9,464,089 · App. 14/329,890 · Granted Oct 11, 2016

Heterocyclic compounds and uses thereof

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.
C07D487/04C07D239/49C07D239/52C07D401/12C07D403/12C07D417/12C07D473/18
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Quick Facts
Patent No.
US 9,464,089
App. No.
14/329,890
Granted
Oct 11, 2016
Kind
B2
Abstract

The present invention relates to pharmaceutical compounds, compositions and methods, especially as they are related to compositions and methods for the treatment and/or prevention of a proliferation disorder, a cancer, a tumor, an inflammatory disease, an autoimmune disease, psoriasis, dry eye or an immunologically related disease, and in some embodiments diseases or disorders related to the dysregulation of kinase such as, but not limited to, EGFR (including HER), Alk, PDGFR, BLK, BMX/ETK, FLT3(D835Y), ITK, TEC, TXK, BTK, or JAK, and the respective pathways.

Claims (42)

1. A compound of Formula (Ia):

wherein

R 1 is

NR c R d wherein

R c is H, C 1-4 alkyl, or 3-7 member cyclic ring, said C 1-4 alkyl or 3-7 member cyclic ring being optionally substituted with OZ, wherein Z is H or C 1-4 alkyl; or said 3-7 member cyclic ring being optionally substituted with C 1-4 alkyl that is further optionally substituted with OZ, wherein Z is H or C 1-4 alkyl; or said 3-7 member cyclic ring being optionally substituted with C 1-4 alkyl that is further optionally substituted with SO 2 (CH 2 ) q H, wherein q is 1-4; or said 3-7 member cyclic ring being optionally substituted with R 8 CO, wherein R 8 is C 1-4 alkyl, and

R d is H, C 1-4 alkyl, or C 1-4 alkenyl; or

3-7 member cyclic ring substituted with R a wherein R a is C 2-8 alkyl substituted with halo, C 1-4 alkoxy or SO 2 (CH 2 ) q H, wherein q is 1-4; or

O(CH 2 ) m SO 2 (CH 2 ) n H, wherein m is 1-4 and n is 1-4;

R 2 is absent, H, halo, C 1-4 alkyl, or C 2-4 alkoxy;

R 3 is C 1-4 alkoxy;

R 5 is absent, H, halo, C 1-4 alkyl, or C 2-4 alkoxy;

R 6 is H, halo, C 1-4 alkyl, or C 2-4 alkoxy;

R 7 is H, halo, C 1-4 alkyl, or C 2-4 alkoxy;

R 9 is H, hydroxyl, halo, C 1-4 alkyl, or C 2-4 alkoxy;

R 10 is H, hydroxyl, halo, C 1-4 alkyl, C 1-4 alkoxy, or alkylamine (NR 11 R 12 ), wherein R 11 and R 12 are independently H or C 1-4 alkyl; or

R 1 and R 5 are part of 3-7 member cyclic ring, said 3-7 member cyclic being optionally substituted with C 1-4 alkyl optionally substituted with OZ or NR 11 R 12 wherein Z, R 11 and R 12 are independently H or C 1-4 alkyl, or said 3-7 member cyclic being optionally substituted with R 8 CO, wherein R 8 is C 1-4 alkyl, or said 3-7 member cyclic being optionally substituted with SO 2 (CH 2 ) q H, wherein q is 1-4; or

R 1 and R 2 are part of 3-7 member cyclic ring, optionally substituted with C 1-4 alkyl, said C 1-4 alkyl further optionally substituted with halo, OZ, or NR 11 R 12 wherein Z, R 11 and R 12 are independently H or C 1-4 alkyl, or one or more members of said 3-7 member cyclic ring is optionally part of a carbonyl group or a sulfonyl group; or

R 2 and R 6 are part of 3-7 member cyclic ring, optionally substituted with C 1-4 alkyl optionally substituted with OZ or NR 11 R 12 wherein Z, R 11 and R 12 are independently H or C 1-4 alkyl;

R 4 is C 2 alkenyl optionally substituted with C 1-4 alkyl, —CH 2 OCH 3 , or —CH 2 N(CH 3 ) 2 ;

X is O or NR b , wherein R b is H, or C 1-8 alkyl optionally substituted with halo;

Y is C, CH optionally substituted with halo, or N;

A is C, CH optionally substituted with halo or N; and

wherein at least one of R 2 , R 3 , R 5 and R 6 is not H;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , which is selected from the group consisting of compound I-3, I-5, I-7, I-9, I-13, I-14, I-16, I-17, I-25a, I-28a, I-29a, I-30a, I-31a, I-32a, I-33a, I-34a, I-35a, I-38a, I-39a, I-42a, I-43a, I-44a, I-45a, I-50a, I-51a, I-52a, I-53a, I-54a, I-55a, I-56a, I-57a, I-58a, I-59a, I-60a, I-66a, I-70a, and I-72a.

3. A pharmaceutical composition comprising a compound of claim 1 admixed with at least one pharmaceutically acceptable carrier or excipient.

4. A compound according to a compound of claim 1 for use in therapy.

5. A compound selected from the group of compounds I-1, I-2, I-4, I-6, I-8, I-12, I-15, I-18, I-19, I-20, I-21, I-22, I-23, I-24, I-25, I-41, and I 23a.

6. The compound of claim 1 , wherein R 4 is C 2 alkenyl.

7. The compound of claim 6 , wherein R 9 is H.

8. The compound of claim 7 , wherein R 10 is H.

9. The compound of claim 8 , wherein A and Y are each independently C or CH.

10. The compound of claim 9 , wherein R 2 and R 5 are each independently absent or H.

11. The compound of claim 10 , wherein R 6 and R 7 are each H.

12. The compound of claim 11 , wherein R 1 is NR c R d and R c is 3-7 member cyclic ring.

13. The compound of claim 12 , wherein the 3-7 member cyclic ring is optionally substituted with R 8 CO, wherein R 8 is C 1-4 alkyl.

14. The compound of claim 13 , wherein R d is C 1-4 alkyl, optionally substituted with OZ or NR 11 R 12 , wherein Z, R 11 , R 12 are independently H or C 1-4 alkyl.

15. The compound of claim 14 , wherein R 1 is NR c R d and R c is a 5 member cyclic ring that comprises a N atom, and the H linked to the N atom is substituted with R 8 CO, wherein R 8 is C 1-4 alkyl.

16. The compound of claim 15 , wherein the H linked to the N atom is substituted with CH 3 CO.

17. The compound of claim 16 , wherein R d is methyl.

18. The compound of claim 17 , wherein R 3 is methoxy.

19. The compound of claim 18 , wherein X is O.

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 Dec 4, 2014
From: XU, XIAO; WANG, XIAOBO; MAO, LONG; ZHAO, LI; XI, BIAO
To: ACEA BIOSCIENCES INC.
Reel/Frame 034533/0305 →
Continuity (3)
Provisional Application 61845342 · Jul 11, 2013
Provisional Application 61923179 · Jan 2, 2014
Related Publication 20150133457A1 · May 14, 2015