IP Library Granted Patent US 10,421,752
Granted Patent B2
US 10,421,752 · App. 15/637,833 · Granted Sep 24, 2019

Compositions and methods for inhibition of the JAK pathway

Inventors: Hui Li (Santa Clara, CA); Sambaiah Thota (Union City, CA); David Carroll (San Francisco, CA); Ankush Argade (Foster City, CA); Kin Tso (San Francisco, CA); Arvinder Sran (Fremont, CA); Jeffrey Clough (Watsonville, CA); Holger Keim (Newbury Park, CA); Somasekhar Bhamidipati (Foster City, CA); Vanessa Taylor (San Francisco, CA); Robin Cooper (St. George Island, FL); Rajinder Singh (Belmont, CA); Brian Wong (Los Altos, CA)
Assignee: Rigel Pharmaceuticals, Inc.
C07D413/12A61K31/343A61K31/436A61K31/505A61K31/506A61K31/538A61K31/5377A61K31/5383A61K31/541A61K31/695A61K38/13A61K39/3955A61K45/06C07D239/42C07D239/48C07D401/12C07D401/14C07D403/04C07D403/12C07D413/14C07D417/12C07D498/04C07F7/0812C07F7/10C07D285/22
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Quick Facts
Patent No.
US 10,421,752
App. No.
15/637,833
Granted
Sep 24, 2019
Kind
B2
Abstract

The invention encompasses compounds having formula I-V and the compositions and methods using these compounds in the treatment of conditions in which modulation of the JAK pathway or inhibition of JAK kinases, particularly JAK3, may be therapeutically useful.

Claims (44)

1. A compound of formula V

or a pharmaceutically acceptable salt thereof, wherein:

X is selected from alkyl, substituted alkyl, alkoxy, substituted alkoxy, amino, substituted amino, carboxyl, carboxyl ester, cyano, halo, nitro, alkenyl, substituted alkenyl, alkynyl or substituted alkynyl;

R is selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, cycloalkyl or substituted cycloalkyl;

each of Z 1 , Z 2 , and Z 3 independently is carbon or nitrogen, wherein if Z 1 is nitrogen then Z 2 and Z 3 are carbon, if Z 2 is nitrogen then Z 1 and Z 3 are carbon, and if Z 3 is nitrogen then Z 1 and Z 2 are carbon, wherein if Z 1 , Z 2 , or Z 3 is nitrogen then SO 2 N(R 4 )R 5 is not attached to the nitrogen;

q is 0, 1, 2 or 3;

each R 3 independently is selected from hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, halo, heterocyclic or substituted heterocyclic;

R 4 and R 5 independently are selected from hydrogen, alkyl, substituted alkyl, acyl or M + , wherein M + is a metal counterion selected from K + , Na + , Li + or + N(R 6 ) 4 , wherein R 6 is hydrogen or alkyl, and the nitrogen of SO 2 NR 4 R 5 is N − ; or

R 4 or R 5 is a divalent counterion selected from Ca 2+ , Mg 2+ , or Ba 2+ , and the nitrogen of SO 2 NR 4 R 5 is N − ; or

R 4 and R 5 together with the nitrogen atom bound thereto, form a heterocyclic or substituted heterocyclic group;

R 7 is selected from hydrogen, alkyl or substituted alkyl; and

V is selected from C 1 -C 3 alkylene, substituted C 1 -C 3 alkylene, C 2 -C 3 alkenylene or substituted C 2 -C 3 alkenylene, wherein one or more of the carbon atoms have been replaced with a heteroatom selected from oxygen, sulfur, S(O), S(O) 2 , or NR 8 , where R 8 is selected from hydrogen or alkyl, or is a bond participating in a —N═C<site of unsaturation;

wherein the compound is not N4-(2,2-dimethyl-3-oxo-4H-benz[1,4]oxazin-6-yl)-5-fluoro-N2-[3-methoxyphenyl-4-(methylamino)sulfonyl]-2,4-pyrimidinediamine.

2. The compound of claim 1 , wherein R 4 and R 5 independently are selected from hydrogen, alkyl, substituted alkyl or acyl.

3. The compound of claim 1 , wherein R 4 and R 5 together with the nitrogen atom bound thereto, form a heterocyclic or substituted heterocyclic group.

4. The compound of claim 1 , wherein the compound has formula VA

or a pharmaceutically acceptable salt thereof, wherein;

X is fluoro or methyl;

q is 0, 1, 2 or 3;

each R 3 independently is selected from hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, halo, heterocyclic or substituted heterocyclic;

R 4 and R 5 independently are selected from hydrogen, alkyl, substituted alkyl, acyl or M + , wherein M + is a metal counterion selected from K + , Na + , Li + or + N(R 6 ) 4 , wherein R 6 is hydrogen or alkyl, and the nitrogen of SO 2 NR 4 R 5 is N − ; or

R 4 or R 5 is a divalent counterion selected from Ca 2+ , Mg 2+ , or Ba 2+ , and the nitrogen of SO 2 NR 4 R 5 is N − ; or

R 4 and R 5 together with the nitrogen atom bound thereto, form a heterocyclic or substituted heterocyclic group;

R 7 is selected from hydrogen, alkyl or substituted alkyl; and

V is selected from C 1 -C 3 alkylene, substituted C 1 -C 3 alkylene, C 2 -C 3 alkenylene or substituted C 2 -C 3 alkenylene, wherein one or more of the carbon atoms have been replaced with a heteroatom selected from oxygen, sulfur, S(O), S(O) 2 , or NR 8 , where R 8 is selected from hydrogen or alkyl, or is a bond participating in a —N═C<site of unsaturation.

5. The compound of claim 1 , wherein the compound has a formula VB

or a pharmaceutically acceptable salt thereof;

X is fluoro or methyl;

q is 0, 1, 2 or 3;

each R 3 independently is selected from hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, cycloalkyl, substituted cycloalkyl, halo, heterocyclic or substituted heterocyclic;

R 4 and R 5 independently are selected from hydrogen, alkyl, substituted alkyl, acyl or M + , wherein M + is a metal counterion selected from K + , Na + , Li + or + N(R 6 ) 4 , wherein R 6 is hydrogen or alkyl, and the nitrogen of SO 2 NR 4 R 5 is N − ; or

R 4 or R 5 is a divalent counterion selected from Ca 2+ , Mg 2+ , and Ba 2+ , and the nitrogen of SO 2 NR 4 R 5 is N; or

R 4 and R 5 together with the nitrogen atom bound thereto, form a heterocyclic or substituted heterocyclic group;

R 7 is selected from hydrogen, alkyl or substituted alkyl; and

V is selected from C 1 -C 3 alkylene, substituted C 1 -C 3 alkylene, C 2 -C 3 alkenylene or substituted C 2 -C 3 alkenylene, wherein one or more of the carbon atoms has been replaced with a heteroatom selected from oxygen, sulfur, S(O), S(O) 2 , or NR 8 , where R 8 is selected from hydrogen or alkyl, or is a bond participating in a —N═C<site of unsaturation.

6. A pharmaceutical formulation comprising a compound of claim 1 and at least one pharmaceutically acceptable excipient, diluent, preservative, or stabilizer, or a combination thereof.

7. A method, comprising contacting a JAK kinase with an amount of a compound according to claim 1 effective to inhibit an activity of the JAK kinase.

8. The method according to claim 7 comprising contacting the JAK kinase in vitro.

9. The method according to claim 7 comprising contacting the JAK kinase in vivo.

10. A method of inhibiting a signal transduction cascade in which JAK3 kinase plays a role, comprising contacting a cell expressing a receptor involved in such a signaling cascade with a compound according to claim 1 .

11. A method, comprising administering to a subject a compound according to claim 1 , in an amount effective to treat or prevent a JAK kinase-mediated disease.

12. A method for treating or preventing allograft transplant rejection in a transplant recipient, the method comprising administering to the transplant recipient a compound according to claim 1 in an amount effective to treat or prevent the rejection.

13. A method for treating a T-cell mediated autoimmune disease, the method comprising administering to a patient suffering from such an autoimmune disease a compound according to claim 1 , in an amount effective to treat the autoimmune disease.

14. A method for treating rheumatoid arthritis, the method comprising administering to a patient a compound according to claim 1 , in an amount effective to treat rheumatoid arthritis.

Assignments (3)
SECURITY INTEREST Recorded May 8, 2026
From: RIGEL PHARMACEUTICALS, INC.
To: MIDCAP FUNDING IV TRUST
Reel/Frame 075576/0880 →
SECURITY INTEREST Recorded Aug 25, 2022
From: RIGEL PHARMACEUTICALS, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 061327/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2017
From: LI, HUI; THOTA, SAMBAIAH; CARROLL, DAVID; ARGADE, ANKUSH; TSO, KIN; SRAN, ARVINDER; CLOUGH, JEFFREY; BHAMIDIPATI, SOMASEKHAR; TAYLOR, VANESSA; COOPER, ROBIN; SINGH, RAJINDER; WONG, BRIAN; KEIM, HOLGER
To: RIGEL PHARMACEUTICALS, INC.
Reel/Frame 043136/0324 →
Continuity (9)
Continuation 14974143 · Dec 18, 2015
Continuation 14315073 · Jun 25, 2014
Continuation 13750632 · Jan 25, 2013
Division 12193627 · Aug 18, 2008
Continuation 11450901 · Jun 8, 2006
Provisional Application 60689032 · Jun 8, 2005
Provisional Application 60706638 · Aug 8, 2005
Provisional Application 60776636 · Feb 24, 2006
Related Publication 20170298054A1 · Oct 19, 2017