IP Library Granted Patent US 10,314,840
Granted Patent B2
US 10,314,840 · App. 15/443,145 · Granted Jun 11, 2019

2,4-pyrimidinediamine compounds and their uses

Inventors: Rajinder Singh (Belmont, CA); Ankush Argade (Foster City, CA); Donald G. Payan (Hillsborough, CA); Susan Molineaux (San Mateo, CA); Sacha J. Holland (San Francisco, CA); Jeffrey Clough (Redwood City, CA); Holger Keim (Irvine, CA); Somasekhar Bhamidipati (Foster City, CA); Catherine Sylvain (San Mateo, CA); Hui Li (Santa Clara, CA); Alexander B. Rossi (Reedsport, OR)
Assignee: Rigel Pharmaceuticals, Inc.
A61K31/505A61K31/506A61K31/519A61K31/538A61K31/5377A61K31/5383A61K31/5395A61K31/551A61K45/06C07D239/48C07D265/36C07D401/12C07D401/14C07D403/12C07D403/14C07D405/12C07D405/14C07D407/14C07D409/12C07D409/14C07D413/10C07D413/12C07D413/14C07D417/12C07D417/14C07D495/04C07D498/04C07D498/14C07F5/027
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Quick Facts
Patent No.
US 10,314,840
App. No.
15/443,145
Granted
Jun 11, 2019
Kind
B2
Abstract

The present invention provides 2,4-pyrimidinediamine compounds that inhibit the IgE and/or IgG receptor signaling cascades that lead to the release of chemical mediators, intermediates and methods of synthesizing the compounds and methods of using the compounds in a variety of contexts, including in the treatment and prevention of diseases characterized by, caused by or associated with the release of chemical mediators via degranulation and other processes effected by activation of the IgE and/or IgG receptor signaling cascades.

Claims (51)

1. A method of inhibiting an Fc receptor signaling cascade and/or regulating or inhibiting a Syk kinase activity in a subject, the method comprising administering a compound to the subject, the compound having a Formula (I)

or a salt thereof, wherein:

R 2 and R 4 are different and independently are each phenyl substituted with one or more of the same or different R 8 groups;

R 5 is fluoro;

R 8 is selected from R a , R b , R a substituted with one or more of the same or different R a or R b , OR a substituted with one or more of the same or different R a , —(CH 2 ) m —R b , —(CHR a ) m —R b , —O—(CH 2 ) m —R b , —O—(CHR a ) m —R b , —C(O)NH—(CH 2 ) m —R b , —C(O)NH—(CHR a ) m —R b , —O—(CH 2 ) m —C(O)NH—(CH 2 ) m —R b , —O—(CHR a ) m —C(O)NH—(CHR a ) m —R b , —NH—(CH 2 ) m —R b —NH—(CHR a ) m —R b ;

each R a is independently selected from (C1-C6) alkyl, (C3-C8) cycloalkyl, cyclohexyl, (C4-C11) cycloalkylalkyl, (C5-C10) aryl, phenyl, (C6-C16) arylalkyl, benzyl, 3-8 membered cycloheteroalkyl, morpholinyl, piperazinyl, homopiperazinyl, piperidinyl, 4-11 membered cycloheteroalkylalkyl, 5-10 membered heteroaryl, or 6-16 membered heteroarylalkyl;

each R b is independently selected from OR a , (C1-C3) haloalkyloxy, —NR c R c , halogen, —CF 3 , —CN, —OCN, —SCN, —NO, NO 2 , —N 3 , —S(O)R a , —S(O) 2 R a , —S(O) 2 OR a , —S(O) 2 NR c R c , —OS(O)R a , —OS(O) 2 R a , —OS(O) 2 OR a , —OS(O) 2 NR c R c , —C(O)R a , —C(O)OR a , —C(O)NR c R c , —C(NH)NR c R c , OC(O)R a , —OC(O)OR a , —OC(O)NR c R c , —OC(NH)NR c R c , —[NHC(O)]R a , —[NHC(O)]OR a , —[NHC(O)]NR c R c or —[NHC(NH)]NR c R c ;

each R c is independently H or R a ;

at least one R 8 is R b ; and

each m is independently an integer from 1 to 3.

2. The method of claim 1 , wherein R 2 is monosubstituted with an R 8 group.

3. The method of claim 2 , wherein the R 8 group is at the para position of R 2 .

4. The method of claim 2 , wherein the R 8 group on R 2 is selected from (C1-C6) alkyl, (C1-C6) branched alkyl, O—C(O)OR a , —O—(CH 2 ) m —C(O)OR a , —O—(CH 2 ) m —R b ,

—C(O)OR a , —O—(CH 2 ) m —NR c R c , —O—C(O)NR c R c , —O—(CH 2 ) m —C(O)NR c R c , —O—C(NH)NR c R c , —O—(CH 2 ) m —C(NH)NR c R c , or —NH—(CH 2 ) m —NR c R c .

5. The method of claim 4 , wherein the R 8 group on R 2 is O—(CH 2 ) m —R b .

6. The method of claim 5 , wherein the R 8 group on R 2 is O—(CH 2 ) m —OR a .

7. The method of claim 1 , wherein R 4 is substituted with at least one R b group.

8. The method of claim 7 , wherein the at least one R b group is selected from —OC(O)R a , —OC(O)OR a , —OC(O)NR c R c , —OC(NH)NR c R c , —[NHC(O)]R a , —[NHC(O)]NR c R c , or —[NHC(NH)] n NR c R c .

9. The method of claim 1 , wherein the R 4 phenyl is monosubstituted.

10. The method of claim 9 , wherein the R 4 phenyl is monosubstituted with an R b group at the meta or para position.

11. The method of claim 1 comprising inhibiting degranulation of immune cells.

12. The method according to claim 11 comprising contacting a cell that degranulates with an amount of the compound effective to regulate or inhibit degranulation of the cell.

13. The method according to claim 1 wherein the subject is an animal.

14. The method according to claim 1 wherein the subject is a human.

15. The method according to claim 1 comprising administering an amount of the compound sufficient to inhibit an Fc receptor signaling cascade.

16. The method according to claim 15 wherein the Fc receptor signaling cascade is an FcεRI signaling cascade, an FcγRI signaling cascade, or both.

17. The method according to claim 15 comprising treating atopic hypersensitivity reactions, Type I hypersensitivity reactions, or both.

18. The method according to claim 17 the atopic hypersensitivity reaction or Type I hypersensitivity reaction is selected from anaphylactic reactions or anaphylactoid reactions.

19. The method according to claim 18 atopic or Type I hypersensitivity reaction is selected from hay fever, allergic conjunctivitis, allergic rhinitis, allergic asthma, atopic dermatitis, eczema, urticaria, mucosal disorders, tissue disorders, gastrointestinal disorders, osteoarthritis, inflammatory bowel disease, ulcerative colitis, Crohn's disease, idiopathic inflammatory bowel disease, irritable bowel syndrome, spastic colon, low grade scarring, scleroderma, increased fibrosis, keloids, post-surgical scars, pulmonary fibrosis, vascular spasms, migraine, reperfusion injury, myocardial infarction, sicca syndrome, and chronic obstructive pulmonary disease (COPD).

20. The method according to claim 1 comprising contacting a Syk kinase or a cell comprising a Syk kinase with an amount of the compound effective to regulate or inhibit Syk kinase activity.

21. A method of inhibiting an Fc receptor signaling cascade, comprising administering an amount of a compound to a human subject, sufficient to inhibit an Fc receptor signaling cascade in the subject, the compound having a Formula (I)

or a salt thereof, wherein:

R 2 and R 4 are different and independently are each phenyl substituted with one or more of the same or different R 8 groups;

R 5 is fluoro;

R 8 is selected from R a , R b , R a substituted with one or more of the same or different R a or R b , OR a substituted with one or more of the same or different R a , —(CH 2 ) m —R b , —(CHR a ) m —R b , —O—(CH 2 ) m —R b , —O—(CHR a ) m —R b , —C(O)NH—(CH 2 ) m —R b , —C(O)NH—(CHR a ) m —R b , —O—(CH 2 ) m —C(O)NH—(CH 2 ) m —R b , —O—(CHR a ) m —C(O)NH—(CHR a ) m —R b , —NH—(CH 2 ) m —R b —NH—(CHR a ) m —R b ;

each R a is independently selected from (C1-C6) alkyl, (C3-C8) cycloalkyl, cyclohexyl, (C4-C11) cycloalkylalkyl, (C5-C10) aryl, phenyl, (C6-C16) arylalkyl, benzyl, 3-8 membered cycloheteroalkyl, morpholinyl, piperazinyl, homopiperazinyl, piperidinyl, 4-11 membered cycloheteroalkylalkyl, 5-10 membered heteroaryl, or 6-16 membered heteroarylalkyl;

each R b is independently selected from OR a , (C1-C3) haloalkyloxy, —NR c R c , halogen, —CF 3 , —CN, —OCN, —SCN, —NO, NO 2 , —N 3 , —S(O)R a , —S(O) 2 R a , —S(O) 2 OR a , —S(O) 2 NR c R c , —OS(O)R a , —OS(O) 2 R a , —OS(O) 2 OR a , —OS(O) 2 NR c R c , —C(O)R a , —C(O)OR a , —C(O)NR c R c , —C(NH)NR c R c , OC(O)R a , —OC(O)OR a , —OC(O)NR c R c , —OC(NH)NR c R c , —[NHC(O)]R a , —[NHC(O)]OR a , —[NHC(O)]NR c R c or —[NHC(NH)]NR c R c ;

each R c is independently H or R a ;

at least one R 8 is R b ; and

each m is independently an integer from 1 to 3.

22. The method of claim 1 , comprising administering the compound to the subject to treat allergic asthma in the subject.

23. A method of regulating or inhibiting a Syk kinase activity in a subject, comprising administering to the subject, an amount of a compound sufficient to regulate or inhibit the Syk kinase activity in the subject, the compound having a Formula (I)

or a salt thereof, wherein:

R 2 and R 4 are different and independently are each phenyl substituted with one or more of the same or different R 8 groups;

R 5 is fluoro;

R 8 is selected from R a , R b , R a substituted with one or more of the same or different R a or R b , OR a substituted with one or more of the same or different R a , —(CH 2 ) m —R b , —(CHR a ) m —R b , —O—(CH 2 ) m —R b , —O—(CHR a ) m —R b , —C(O)NH—(CH 2 ) m —R b , —C(O)NH—(CHR a ) m —R b , —O—(CH 2 ) m —C(O)NH—(CH 2 ) m —R b , —O—(CHR a ) m —C(O)NH—(CHR a ) m —R b , —NH—(CH 2 ) m —R b —NH—(CHR a ) m —R b ;

each R a is independently selected from (C1-C6) alkyl, (C3-C8) cycloalkyl, cyclohexyl, (C4-C11) cycloalkylalkyl, (C5-C10) aryl, phenyl, (C6-C16) arylalkyl, benzyl, 3-8 membered cycloheteroalkyl, morpholinyl, piperazinyl, homopiperazinyl, piperidinyl, 4-11 membered cycloheteroalkylalkyl, 5-10 membered heteroaryl, or 6-16 membered heteroarylalkyl;

each R b is independently selected from OR a , (C1-C3) haloalkyloxy, —NR c R c , halogen, —CF 3 , —CN, —OCN, —SCN, —NO, NO 2 , —N 3 , —S(O)R a , —S(O) 2 R a , —S(O) 2 OR a , —S(O) 2 NR c R c , —OS(O)R a , —OS(O) 2 R a , —OS(O) 2 OR a , —OS(O) 2 NR c R c , —C(O)R a , —C(O)OR a , —C(O)NR c R c , —C(NH)NR c R c , OC(O)R a , —OC(O)OR a , —OC(O)NR c R c , —OC(NH)NR c R c , —[NHC(O)]R a , —[NHC(O)]OR a , —[NHC(O)]NR c R c or —[NHC(NH)]NR c R c ;

each R c is independently H or R a ;

at least one R 8 is R b ; and

each m is independently an integer from 1 to 3.

Assignments (2)
SECURITY INTEREST Recorded Aug 25, 2022
From: RIGEL PHARMACEUTICALS, INC.
To: MIDCAP FINANCIAL TRUST
Reel/Frame 061327/0712 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2017
From: SINGH, RAJINDER; ARGADE, ANKUSH; PAYAN, DONALD G.; MOLINEAUX, SUSAN; HOLLAND, SACHA J.; CLOUGH, JEFFREY; KEIM, HOLGER; BHAMIDIPATI, SOMASEKHAR; SYLVAIN, CATHERINE; LI, HUI; ROSSI, ALEXANDER B.
To: RIGEL PHARMACEUTICALS, INC.
Reel/Frame 042041/0262 →
Continuity (14)
Continuation 14858661 · Sep 18, 2015
Continuation 14626471 · Feb 19, 2015
Continuation 14333163 · Jul 16, 2014
Continuation 13961780 · Aug 7, 2013
Continuation 13759835 · Feb 5, 2013
Continuation 13288813 · Nov 3, 2011
Continuation 12762178 · Apr 16, 2010
Continuation 11539049 · Oct 5, 2006
Continuation 10355543 · Jan 31, 2003
Provisional Application 60353333 · Feb 1, 2002
Provisional Application 60353267 · Feb 1, 2002
Provisional Application 60399673 · Jul 29, 2002
Provisional Application 60434277 · Dec 17, 2002
Related Publication 20170246167A1 · Aug 31, 2017