IP Library Granted Patent US 10,364,240
Granted Patent B2
US 10,364,240 · App. 15/697,414 · Granted Jul 30, 2019

Aryl sulfonamides

Inventors: Solomon Ungashe (Fremont, CA); John J. Wright (Redwood City, CA); Andrew Pennell (San Francisco, CA); Zheng Wei (Union City, CA); Anita Melikian (San Francisco, CA)
Assignee: ChemoCentryx. Inc.
C07D417/12A61K31/443A61K31/4409A61K31/4439A61K31/4545A61K31/496A61K31/5377A61K31/541A61K45/06C07D213/26C07D213/50C07D213/52C07D213/70C07D213/74C07D213/84C07D213/89C07D239/26C07D241/12C07D401/12C07D405/12C07D409/12C07D413/12
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Quick Facts
Patent No.
US 10,364,240
App. No.
15/697,414
Granted
Jul 30, 2019
Kind
B2
Abstract

Compounds are provided that act as potent antagonists of the CCR9 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR9. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR9-mediated diseases, and as controls in assays for the identification of CCR9 antagonists.

Claims (42)

1. A compound of the formula (I), or a salt thereof:

where

X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR 1 , —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR i (CO)NR 2 R 3 , unsubstituted C 1-8 alkyl, unsubstituted C 2-8 alkenyl, unsubstituted C 2-8 alkynyl;

R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl; or

two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted 5-, 6- or 7-membered ring;

Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted C 1-4 alkyl;

R 4 is selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl;

L is —C(O)—, —S—, —SO— or —S(O) 2 —; and

Z is an unsubstituted or substituted heteroaryl selected from pyrazolyl, imidazolyl, thiazolyl, and triazolyl.

2. The compound of claim 1 , where L is —CO—.

3. A composition comprising a pharmaceutically acceptable carrier and a compound of claim 1 .

4. A method for treating a CCR9-mediated condition or disease comprising administering to a subject a safe and effective amount of a compound of the formula (I), or a salt thereof:

where

X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR 1 , —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR 1 (CO)NR 2 R 3 , unsubstituted C 1-8 alkyl, unsubstituted C 2-8 alkenyl, unsubstituted C 2-8 alkynyl;

R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl; or

two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted 5-, 6- or 7-membered ring;

Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted C 1-4 alkyl;

R 4 is selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl;

L is —C(O)—, —S—, —SO— or —S(O) 2 —; and

Z is an unsubstituted or substituted heteroaryl selected from pyrazolyl, imidazolyl, thiazolyl, and triazolyl.

5. The method of claim 4 , where the CCR9-mediated disease or condition is an inflammatory condition.

6. The method of claim 4 , where the CCR9-mediated disease or condition is an immunoregulatory disorder.

7. The method of claim 4 , where the CCR9-mediated condition or disease is inflammatory bowel disease.

8. The method of claim 4 , where the CCR9-mediated condition or disease is selected from the group consisting of an allergic disease, psoriasis, atopic dermatitis, asthma, fibrotic diseases and graft rejection.

9. The method of claim 4 , where the CCR9-mediated condition or disease is selected from the group consisting of immune mediated food allergies and autoimmune diseases.

10. The method of claim 9 , where the CCR9-mediated condition or disease is Celiac disease or rheumatoid arthritis.

11. The method of claim 4 , where the administering is oral, parenteral, rectal, transdermal, sublingual, nasal or topical.

12. The method of claim 4 , where the compound is administered in combination with an anti-inflammatory or analgesic agent.

13. The method of claim 4 , where the CCR9-mediated disease or condition is leukemia or a solid tumor.

14. The method of claim 4 , where the CCR9-mediated disease or condition is thymoma or a thymic carcinoma.

15. The method of claim 13 , where the CCR9-mediated disease or condition is acute lymphocytic leukemia.

16. A method of modulating CCR9 function in a cell, comprising contacting the cell with a CCR9 modulating amount of a compound of the formula (I), or a salt thereof:

where

X represents from 1 to 4 substituents independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 1 , —C(O)R 1 , —CO 2 R 1 , —O(CO)R 1 , —C(O)NR 1 R 2 , —OC(O)NR 1 R 2 , —SR 1 , —SOR 1 , —SO 2 R 1 , —SO 2 NR 1 R 2 , —NR 1 R 2 , —NR 1 C(O)R 2 , —NR 1 C(O) 2 R 2 , —NR 1 SO 2 R 2 , —NR 1 (CO)NR 2 R 3 , unsubstituted C 1-8 alkyl, unsubstituted C 2-8 alkenyl, unsubstituted C 2-8 alkynyl;

R 1 , R 2 and R 3 are each independently selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, unsubstituted C 2-6 alkynyl; or

two of R 1 , R 2 and R 3 together with the atom(s) to which they are attached, may form an unsubstituted 5-, 6- or 7-membered ring;

Y represents from 1 to 3 substituents, each independently selected from the group consisting of halogen, —CN, —NO 2 , —OH, —OR 4 , —C(O)R 4 , —CO 2 R 4 , —SR 4 , —SOR 4 , —SO 2 R 4 , and unsubstituted C 1-4 alkyl;

R 4 is selected from the group consisting of hydrogen, unsubstituted C 1-6 haloalkyl, unsubstituted C 1-6 alkyl, unsubstituted C 2-6 alkenyl, and unsubstituted C 2-6 alkynyl;

L is —C(O)—, —S—, —SO— or —S(O) 2 —; and

Z is an unsubstituted or substituted heteroaryl selected from pyrazolyl, imidazolyl, thiazolyl, and triazolyl.

17. The method of claim 7 , where the CCR9-mediated condition or disease is Crohn's disease or ulcerative colitis.

18. The method of claim 13 , where the leukemia or solid tumor is metastatic.

Assignments (2)
ASSIGNEE CHANGE OF ADDRESS Recorded Jun 27, 2023
From: CHEMOCENTRYX, INC.
To: CHEMOCENTRYX, INC.
Reel/Frame 064144/0685 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 14, 2017
From: UNGASHE, SOLOMON; WRIGHT, JOHN J.; PENNELL, ANDREW; WEI, ZHENG; MELIKIAN, ANITA
To: CHEMOCENTRYX, INC.
Reel/Frame 043586/0441 →
Continuity (8)
Continuation 14551438 · Nov 24, 2014
Continuation 13852167 · Mar 28, 2013
Continuation 13245568 · Sep 26, 2011
Continuation 12137006 · Jun 11, 2008
Continuation In Part 10846241 · May 13, 2004
Continuation In Part 10716170 · Nov 17, 2003
Provisional Application 60427670 · Nov 18, 2002
Related Publication 20170369483A1 · Dec 28, 2017