IP Library Granted Patent US 8,119,798
Granted Patent B2
US 8,119,798 · App. 12/375,184 · Granted Feb 21, 2012

P38 kinase inhibitors

Assignee: GlaxoSmithKline LLC
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Quick Facts
Patent No.
US 8,119,798
App. No.
12/375,184
Granted
Feb 21, 2012
Kind
B2
Abstract

Compounds of formula (I) and (II) are disclosed, as well as methods for their identification, their preparation, pharmaceutical compositions containing them, and their use in treating disease. The compounds inhibit the production of TNF-alpha and interleukins (IL) by the inhibition of p38 kinase. They are useful in the treatment of inflammation and arthritis.

Claims (26)

1. A compound of formula II-3:

or a pharmaceutically acceptable salt thereof, wherein:

R 1 is (C 1 -C 6 )alkyl optionally substituted with 1, 2, or 3 R 6 ;

 is (C 3 -C 6 )cycloalkyl or aryl optionally substituted on carbon with 1, 2, or 3 R 6 ;

R 2 is hydrogen or (C 1 -C 6 )alkyl which may be optionally substituted on carbon with 1, 2, or 3 R 6 ;

R 3 is —OH, —O—(C 1 -C 6 )alkyl, —NH 2 , —NH(C 1 -C 6 )alkyl), —N((C 1 -C 6 )alkyl) 2 , —NH(O—C 1 -C 6 )alkyl), —O-aralkyl, any of which may be optionally substituted on carbon with 1, 2, or 3 R 6 ;

R 4a is hydrogen, (C 1 -C 6 )alkyl, or (C 3 -C 6 )cycloalkyl which may be optionally substituted on carbon with 1, 2, or 3 R 6 ;

R 4b is hydrogen, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, aryl, heteroaryl, aralkyl, or heteroaralkyl, any of which may be optionally substituted on carbon with 1, 2, or 3 R 6 ; or

R 4a and R 4b , together with the carbon to which they are attached, form a (C 3 -C 6 )cycloalkyl, aryl or heteroaryl group, any of which may be optionally substituted on carbon with 1, 2, or 3 R 6 ;

R 5 is hydrogen, (C 1 -C 6 )alkyl, or (C 3 -C 6 )cycloalkyl;

R 6 is halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, hydroxy, amino, —NH(C 1 -C 6 )alkyl, —N((C 1 -C 6 )alkyl) 2 , aryl, heteroaryl, (C 3 -C 7 )cycloalkyl, (C 1 -C 6 )alkyl, (C 2 -C 6 )alkenyl, (C 2 -C 6 )alkynyl, (C 1 -C 6 )alkoxy, (C 2 -C 6 )alkenyloxy, (C 2 -C 6 )alkynyloxy, (C 1 -C 6 )alkylthio, (C 1 -C 6 )alkylsulfinyl, (C 1 -C 6 )alkylsulfonyl, amino, (C 1 -C 6 )alkylamino, di-[(C 1 -C 6 )alkyl]amino, formyl, —C(═O)(C 1 -C 6 )alkyl, —C(═N)(C 1 -C 6 )alkyl, carboxy, —CO 2 (C 1 -C 6 )alkyl, —CONH 2 , —C(═N)NH 2 , —C(═N)NH(C 1 -C 6 )alkyl), —C(═N)N(C 1 -C 6 )alkyl) 2 , —CONH(C 1 -C 6 )alkyl, —CON((C 1 -C 6 )alkyl) 2 , —OC(O)(C 1 -C 6 )alkyl, —OC(O)NH 2 , —OC(O)NH(C 1 -C 6 )alkyl, —OC(O)NH((C 1 -C 6 )alkyl) 2 , —NHC(O)(C 1 -C 6 )alkyl, —N(C 1 -C 6 )alkyl-C(O)(C 1 -C 6 )alkyl, —NH—C(O)NH 2 , —N(C 1 -C 6 )alkyl-C(O)NH 2 , —N(C 1 -C 6 )alkyl-C(O)NH(C 1 -C 6 )alkyl, —N(C 1 -C 6 )alkyl-C(O)NH(C 1 -C 6 )alkyl) 2 , —NH—C(O)NH(C 1 -C 6 )alkyl) 2 , —NH—(C 1 -C 6 )alkylsulfamoyl, N,N-di-[(C 1 -C 6 )alkyl]sulfamoyl, (C 1 -C 6 )alkylsulfonylamino, or —N—(C 1 -C 6 )alkyl-(C 1 -C 6 )alkylsulfonylamino, any of which may be optionally substituted on carbon with R 7 ;

R 7 is halogen, trifluoromethyl, trifluoromethoxy, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy, cyano, nitro, or hydroxyl; and

R 8 is selected from hydrogen and (C 1 -C 6 )alkyl.

2. The compound of claim 1 , wherein R 1 is selected from the group consisting of methyl, optionally substituted on carbon with 1 or 2 amino, halogen or alkoxy.

3. The compound of claim 1 , wherein

is selected from the group consisting of cyclohexyl, cyclopentyl, cyclobutyl, cyclopropyl, and phenyl.

4. The compound of claim 1 , wherein R 2 is hydrogen or methyl.

5. The compound claim 1 , wherein R 3 is selected from the group consisting of —OH, —OMe, —OEt, —NH 2 , —NHMe, —NMe 2 and —NH—OMe.

6. The compound of claim 1 , wherein R 5 is selected from the group consisting of hydrogen, methyl and cyclohexyl.

7. The compound of claim 1 , wherein R 6 is selected from the group consisting of chloro, fluoro, trifluoromethyl, trifluoromethoxy, cyano, nitro, hydroxyl, amino and methyl.

8. The compound of claim 1 , wherein R 7 is selected from the group consisting of chloro, fluoro, trifluoromethyl, trifluoromethoxy, cyano, nitro and hydroxyl.

9. A compound selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

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

11. A method of inhibiting p38 kinase activity in a subject having rheumatoid arthritis or a biological sample obtained from a subject having rheumatoid arthritis, comprising administering to the subject or contacting the biological sample with an effective amount of a composition of claim 10 , such that p38 kinase activity is inhibited.

12. A method of treating arthritis in a subject, comprising administering to a subject in need thereof an effective amount of a composition of claim 10 , such that the arthritis is treated.

Assignments (2)
MERGER Recorded Apr 12, 2011
From: PRAECIS PHARMACEUTICALS INCORPORATED
To: GLAXOSMITHKLINE LLC
Reel/Frame 026116/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2009
From: CLARK, MATTHEW
To: PRAECIS PHARMACEUTICALS INCORPORATED
Reel/Frame 023528/0982 →
Continuity (2)
Provisional Application 60821116 · Aug 1, 2006
Related Publication 20100120772A1 · May 13, 2010