IP Library Granted Patent US 8,513,289
Granted Patent B2
US 8,513,289 · App. 13/266,043 · Granted Aug 20, 2013

P38 kinase inhibiting agents

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Quick Facts
Patent No.
US 8,513,289
App. No.
13/266,043
Granted
Aug 20, 2013
Kind
B2
Abstract

Compounds described by the chemical formula (I) or pharmaceutically acceptable salts thereof: Formula (I); are inhibitors of p38 and are useful in the treatment of inflammation such as in the treatment of asthma, COPD, ARDS, rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions; inflamed joints, eczema, psoriasis or other inflammatory skin conditions such as sunburn; inflammatory eye conditions including conjunctivitis; pyresis, pain and other conditions associated with inflammation.

Claims (106)

1. A compound represented by chemical formula (I)

or a pharmaceutically acceptable salt thereof, wherein:

L is selected from the group consisting of:

(a) —C(O)—,

(b) —CH(OH)—

(c) —CH(NR 3 R 4 )—

(d) —C(═NOR 3 )—,

(e) —CH 2 —, and

(f) —S(O) n —, wherein n is 0, 1 or 2;

Ar 1 is an optionally mono, di- or tri-substituted phenyl or heteroaromatic ring of 6 atoms, wherein the heteroaromatic ring may contain 1, 2 or 3 heteroatoms selected from N, S and O, wherein the substituents are independently selected from the group consisting of:

(a) halo,

(b) —C 1-4 alkyl,

(c) —O—C 1-4 alkyl,

(d) —CF 3 ,

(e) —NH 2 ,

(f) —NH—CH 3 ,

(g) —CN,

(h) —C(O)NH 2 , and

(i) —S(O) n —CH 3 ;

Ar 2 is an optionally substituted thiadiazole or oxadiazole ring wherein thesubstituent is a phenyl or a 5 or 6 membered mono-cyclic heteroaromatic or heterocyclic ring, or a bicyclic heteroaromatic or heterocyclic ring of 9 or 10 atoms, said heteroaromatic or heterocyclic ring containing 1, 2 or 3 hetero atoms selected from the group consisting of S, O and N, where in said phenyl, heteroaromatic or heterocyclic ring is optionally mono or di-substituted with substituents independently selected from the group consisting of:

(a) halo,

(b) —C 1-6 alkyl, optionally substituted with 1 to 4 fluorine atoms

(c) —O—C 1-6 alkyl,

(d) —CF 3 ,

(e) —NH 2 ,

(f) —NH—CH 3 ,

(g) —NH—CH 2 CF 3 ,

(h) —C(O)-morpholinyl,

(i) —C(O)—NR 1 R 2 ,

(j) —C(O)OH,

(k) —CN,

(l) oxo, and

(m) C 3-6 cycloalkyl;

R 1 , R 2 , R 3 and R 4 are independently selected from the group consisting of

(a) hydrogen, and

(b) C 1-4 alkyl,

or R 1 and R 2 or R 3 and R 4 may be joined together to form a 5 or 6 membered saturated ring, said ring optionally containing a heteroatom selected from S, N and O.

2. The compound according to claim 1 , wherein

L is selected from the group consisting of:

(a) —C(O)—, and

(b) —CH 2 —.

3. The compound according to claim 2 , wherein

L is —C(O)—.

4. The compound according to claim 1 , wherein

Ar 1 is an optionally mono, di- or tri-substituted phenyl or heteroaromatic ring of 6 atoms, wherein the heteroaromatic ring may contain 1, 2 or 3 heteroatoms selected from N, S and O, wherein the substituents are independently selected from the group consisting of:

(a) halo,

(b) —C 1-4 alkyl, and

(c) —O—C 1-4 alkyl.

5. The compound according to claim 4 , wherein

Ar 1 is an optionally mono, di- or tri-substituted phenyl or pyridyl, wherein the substituents are independently selected from the group consisting of

(a) fluoro,

(b) chloro, and

(c) —CH 3 .

6. The compound according to claim 5 , wherein

Ar 1 is an optionally mono, di- or tri-substituted phenyl, wherein the substituents are independently selected from the group consisting of

(a) fluoro,

(b) chloro, and

(c) —CH 3 .

7. The compound according to claim 1 wherein

Ar 2 is an optionally substituted thiadiazolyl.

8. The compound according to claim 7 wherein

the substituent is phenyl or a 5 or 6 membered mono-cyclic heteroaromatic or heterocyclic ring, or a 9 or 10 atom bicyclic heteroaromatic or heterocyclic ring, said hetero aromatic or heterocyclic ring containing 1, 2 or 3 hetero atoms selected from the group consisting of S, O and N, where in said phenyl, heteroaromatic or heterocyclic ring is optionally mono or di-substituted with substituents independently selected from the group consisting of:

(a) halo,

(b) —C 1-6 alkyl, optionally substituted with CF 3 ,

(c) —O—C 1-4 alkyl,

(d) —CF 3 , and

(e) C 3-6 cycloalkyl.

9. The compound according to claim 8 wherein

the substituent is phenyl or a 5 or 6 membered mono-cyclic heteroaromatic or heterocyclic ring, said hetero aromatic or heterocyclic ring containing 1, 2 or 3 hetero atoms selected from the group consisting of S, O and N, where in said phenyl, heteroaromatic or heterocyclic ring is optionally mono or di-substituted with substituents independently selected from the group consisting of:

(a) halo,

(b) —C 1-6 alkyl, optionally substituted with CF 3 ,

(c) —O—C 1-4 alkyl,

(d) —CF 3 , and

(e) C 3-6 cycloalkyl.

10. The compound according to claim 1 wherein

R 1 , R 2 , R 3 and R 4 are independently selected from the group consisting of

(a) hydrogen, and

(b) methyl.

11. A compound according to claim 1 of Formula I

or a pharmaceutically acceptable salt thereof, wherein:

L is —C(O)—;

Ar l is an optionally a mono, di- or tri-substituted phenyl, wherein the phenyl is substituted with substituents independently selected from the group consisting of:

(a) F,

(b) Cl,

(c) —C 1-4 alkyl, and

(d) —O—C 1-4 alkyl;

Ar 2 is optionally substituted thiadiazolyl, and

the substituent is phenyl or a 5 or 6 membered mono-cyclic heteroaromatic or heterocyclic ring, said hetero aromatic or heterocyclic ring containing 1, 2 or 3 hetero atoms selected from the group consisting of S, O and N, where in said phenyl, heteroaromatic or heterocyclic ring is optionally mono or di-substituted with substituents independently selected from the group consisting of:

(a) halo,

(b) —C 1-4 alkyl,

(c) —O—C 1-4 alkyl,

(d) —CF 3 ,

(e) C 3-6 cycloalkyl.

12. A compound according to claim 1 having the following structure

or a pharmaceutically acceptable salt thereof, wherein:

Ar 2 is optionally substituted thiadiazolyl, wherein the substituent is phenyl or a 5 or 6 membered mono-cyclic heteroaromatic or heterocyclic ring, said hetero aromatic or heterocyclic ring containing 1, 2 or 3 hetero atoms selected from the group consisting of S, O and N, where in said phenyl, heteroaromatic or heterocyclic ring is optionally mono or di-substituted with substituents independently selected from the group consisting of:

(a) halo,

(b) —C 2-6 alkyl,

(c) —O—C 1-4 alkyl, and

(d) —CF 3 .

13. The compound according to claim 1 , selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

14. A pharmaceutical composition comprising an inert carrier and an effective amount of a compound according to claim 1 .

15. A compound having the following structure

or a pharmaceutically acceptable salt thereof.

16. A pharmaceutical composition comprising an inert carrier and an effective amount of the compound of claim 15 .

Assignments (3)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
CHANGE OF NAME Recorded Jul 9, 2013
From: MERCK & CO., INC.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 030761/0202 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2013
From: KOYAMA, HIROO; SAHOO, SOUMYA P.; XU-QIANG, GINGER; MILLER, DANIEL J.
To: MERCK & CO., INC.
Reel/Frame 030121/0731 →