IP Library Granted Patent US 10,092,583
Granted Patent B2
US 10,092,583 · App. 15/387,557 · Granted Oct 9, 2018

Imidazopyridines Syk inhibitors

Inventors: Peter A. Blomgren (Issaquah, WA); Kevin S. Currie (North Bend, WA); Jeffrey E. Kropf (Issaquah, WA); Seung H. Lee (Sammamish, WA); Scott A. Mitchell (Kenmore, WA); Aaron C. Schmitt (Hamden, CT); Jianjun Xu (Seattle, WA); Zhongdong Zhao (Bellevue, WA)
Assignee: Gilead Connecticut, Inc.
A61K31/69A61K31/437A61K31/444A61K31/4545A61K31/496A61K31/498A61K31/4985A61K31/506A61K31/517A61K31/538A61K31/5377A61K31/5383
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,092,583
App. No.
15/387,557
Granted
Oct 9, 2018
Kind
B2
Abstract

Certain imidazopyridines and pharmaceutical compositions thereof are provided herein. Methods of treating patients suffering from certain diseases and disorders responsive to the inhibition of Syk activity, which comprises administering to such patients an amount of at least one chemical entity effective to reduce signs or symptoms of the disease or disorder are provided. Also provided are methods for determining the presence or absence of Syk kinase in a sample.

Claims (45)

1. A method for inhibiting Syk activity in a patient having a disease responsive to the inhibition of Syk activity, comprising administering to the patient an effective amount of at least one chemical entity chosen from compounds of Formula I:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is optionally substituted phenyl;

R 2 is 2,3-dimethyl-2H-indazol-6-yl, 1H-indazolyl-6-yl, 1-methyl-1H-indazol-5-yl, 1-methyl-1H-indazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-3-one-6-yl, 1-(2-hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one-5-yl, 3-amino-1H-indazol-6-yl, 1H-pyrrolo[3,2-b]pyridine-6-yl, 1,3-benzoxazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-6-yl, 2-hydroxyquinoxalin-7-yl, 3-aminoquinolin-6-yl, 2,3-dihydro-1H-indol-6-yl, 1H,2H,3H-pyrido[2,3-b][1,4]oxazin-2-one, (3-hydroxyethyl)-1H-indol-6-yl, benzothiazolyl, 2-aminoquinazolin-6-yl, 3,3-dimethylindolin-2-one, 2,3-dihydro-1H-indol-2-one, 4-fluoro-1H-indazol-6-yl, 5-fluoro-1H-indazol-6-yl, or 3-amino-1H-indazol-6-yl; and

R 3 is hydrogen, lower alkyl, halogen, carboxamido, or CO 2 H,

wherein the disease responsive to the inhibition of Syk activity is an inflammatory disorder, an allergic disorder, an autoimmune disease, or cancer.

2. The method according to claim 1 , wherein R 1 is phenyl optionally substituted with one or more groups independently chosen from

hydroxy;

—NR b R c , wherein R b is chosen from hydrogen and C 1 -C 6 alkyl optionally substituted with one or two groups independently chosen from hydroxy and —OC 1 -C 4 alkyl, and R c is independently chosen from hydrogen and C 1 -C 4 alkyl optionally substituted with one or two groups independently chosen from hydroxy and —OC 1 -C 4 alkyl;

heterocycloalkyl optionally substituted with one or two groups independently chosen from hydroxy, C 3 -C 6 cycloalkyl, C 1 -C 4 alkyl, —C 1 -C 4 alkyl-OH, —C 1 -C 4 alkyl-O—C 1 -C 4 alkyl, —C 1 -C 4 alkyl-NH 2 , —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —NH(C 1 -C 4 alkyl), —C(O)(C 1 -C 4 alkyl), —C(O)(C 1 -C 4 alkyl-OH), and —OC 1 -C 4 alkyl;

—OC 1 -C 6 alkyl optionally substituted with one or two groups independently chosen from hydroxy, C 3 -C 6 cycloalkyl, C 1 -C 4 alkyl, —C 1 -C 4 alkyl-OH, —C 1 -C 4 alkyl-O—C 1 -C 4 alkyl, —C 1 -C 4 alkyl-NH 2 , —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —NH(C 1 -C 4 alkyl), and —OC 1 -C 4 alkyl; and

C 1 -C 6 alkyl optionally substituted with one or two groups independently chosen from hydroxy, C 3 -C 6 cycloalkyl, C 1 -C 4 alkyl, —C 1 -C 4 alkyl-OH, —C 1 -C 4 alkyl-O—C 1 -C 4 alkyl, —C 1 -C 4 alkyl-NH 2 , —N(C 1 -C 4 alkyl)(C 1 -C 4 alkyl), —NH(C 1 -C 4 alkyl), and —OC 1 -C 4 alkyl.

3. A method for inhibiting Syk activity in a patient having a disease responsive to the inhibition of Syk activity, comprising administering to the patient an effective amount of at least one chemical entity chosen from compounds of Formula I:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is optionally substituted phenyl;

R 2 is 1H-indazolyl-6-yl, 1-methyl-1H-indazol-5-yl, 1-methyl-1H-indazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-3-one-6-yl, 1,3-benzoxazol-6-yl, 3-aminoquinolin-6-yl, 1H-pyrrolo[3,2-b]pyridin-6-yl, or 2,3-dihydro-1H-indol-2-one-6-yl; and

R 3 is hydrogen, lower alkyl, halogen, carboxamido, or CO 2 H,

wherein the disease responsive to the inhibition of Syk activity is an inflammatory disorder, an allergic disorder, an autoimmune disease, or cancer.

4. A method for inhibiting Syk activity in a patient having a disease responsive to the inhibition of Syk activity, comprising administering to the patient an effective amount of at least one chemical entity chosen from compounds of Formula I:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is optionally substituted phenyl;

R 2 is 2,3-dimethyl-2H-indazol-6-yl, 1H-indazolyl-6-yl, 1-methyl-1H-indazol-5-yl, 1-methyl-1H-indazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-3-one-6-yl, 1-(2-hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one-5-yl, 3-amino-1H-indazol-6-yl, 1H-pyrrolo[3,2-b]pyridine-6-yl, 1,3-benzoxazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-6-yl, 2-hydroxyquinoxalin-7-yl, 3-aminoquinolin-6-yl, 2,3-dihydro-1H-indol-6-yl, 1H,2H,3H-pyrido[2,3-b][1,4]oxazin-2-one, (3-hydroxyethyl)-1H-indol-6-yl, benzothiazolyl, 2-aminoquinazolin-6-yl, 3,3-dimethylindolin-2-one, 2,3-dihydro-1H-indol-2-one, 4-fluoro-1H-indazol-6-yl, 5-fluoro-1H-indazol-6-yl, or 3-amino-1H-indazol-6-yl; and

R 3 is chosen from hydrogen and methyl,

wherein the disease responsive to the inhibition of Syk activity is an inflammatory disorder, an allergic disorder, an autoimmune disease, or cancer.

5. A method for inhibiting Syk activity in a patient having a disease responsive to the inhibition of Syk activity, comprising administering to the patient an effective amount of at least one chemical entity chosen from compounds of Formula I:

or a pharmaceutically acceptable salt thereof, wherein

R 1 is optionally substituted phenyl;

R 2 is 2,3-dimethyl-2H-indazol-6-yl, 1H-indazolyl-6-yl, 1-methyl-1H-indazol-5-yl, 1-methyl-1H-indazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-3-one-6-yl, 1-(2-hydroxyethyl)-1H-benzo[d]imidazol-2(3H)-one-5-yl, 3-amino-1H-indazol-6-yl, 1H-pyrrolo[3,2-b]pyridine-6-yl, 1,3-benzoxazol-6-yl, 3,4-dihydro-2H-1,4-benzoxazin-6-yl, 2-hydroxyquinoxalin-7-yl, 3-aminoquinolin-6-yl, 2,3-dihydro-1H-indol-6-yl, 1H,2H,3H-pyrido[2,3-b][1,4]oxazin-2-one, (3-hydroxyethyl)-1H-indol-6-yl, benzothiazolyl, 2-aminoquinazolin-6-yl, 3,3-dimethylindolin-2-one, 2,3-dihydro-1H-indol-2-one, 4-fluoro-1H-indazol-6-yl, 5-fluoro-1H-indazol-6-yl, or 3-amino-1H-indazol-6-yl; and

R 3 is hydrogen,

wherein the disease responsive to the inhibition of Syk activity is an inflammatory disorder, an allergic disorder, an autoimmune disease, or cancer.

6. A method for inhibiting Syk activity in a patient having a disease responsive to the inhibition of Syk activity, comprising administering to the patient an effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof, wherein the disease responsive to the inhibition of Syk activity is an inflammatory disorder, an allergic disorder, an autoimmune disease, or cancer.

7. The method according to claim 1 , wherein the patient is a human.

8. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is cancer.

9. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is B-cell lymphoma or leukemia.

10. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is rheumatoid arthritis.

11. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is allergic rhinitis.

12. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is adult respiratory distress syndrome (ARDs).

13. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is an allergy-induced inflammatory disease.

14. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is multiple sclerosis.

15. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is an autoimmune disease.

16. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is an inflammatory disease.

17. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is acute inflammatory reaction.

18. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is an allergic disorder.

19. The method according to claim 1 , wherein the disease responsive to inhibition of Syk activity is polycystic kidney disease.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2020
From: GILEAD CONNECTICUT, INC.
To: KRONOS BIO, INC.
Reel/Frame 053927/0969 →
MERGER AND CHANGE OF NAME Recorded Sep 17, 2020
From: COUGAR MERGER SUB, INC.; CGI PHARMACEUTICALS, INC.; CGI PHARMACEUTICALS, INC.
To: GILEAD CONNECTICUT, INC.
Reel/Frame 053799/0190 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2018
From: BLOMGREN, PETER A.; CURRIE, KEVIN S.; KROPF, JEFFREY E.; LEE, SEUNG H.; MITCHELL, SCOTT A.; SCHMITT, AARON C.; XU, JIANJUN; ZHAO, ZHONGDONG
To: GILEAD CONNECTICUT, INC.
Reel/Frame 045593/0748 →
Continuity (4)
Division 13806094
Provisional Application 61313223 · Mar 12, 2010
Provisional Application 61312771 · Mar 11, 2010
Related Publication 20170095490A1 · Apr 6, 2017
Cited By (1)
US 12,263,163