IP Library Granted Patent US 9,745,295
Granted Patent B2
US 9,745,295 · App. 14/786,464 · Granted Aug 29, 2017

Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors

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Quick Facts
Patent No.
US 9,745,295
App. No.
14/786,464
Granted
Aug 29, 2017
Kind
B2
Abstract

The invention provides certain thiazole-substituted aminoheteroaryl compounds of the Formula (I) or pharmaceutically acceptable salts thereof, wherein X 1 , X 2 , X 3 , X 4 , Y 1 , Y 2 , Y 3 , Y 4 , and R 4 are as defined herein. The invention also provides pharmaceutical compositions comprising such compounds, and methods of using the compounds for treating diseases or conditions mediated by Spleen Tyrosine Kinase (Syk).

Claims (44)

1. A compound of the Formula (I)

or a pharmaceutically acceptable salt thereof, wherein

the group

R 1 is selected from the group consisting of:

(a) H;

(a) C 1 -C 3 alkyl;

(c) C 1 -C 3 fluoroalkyl;

(d) C 1 -C 3 alkoxy; and

(e) C 3 -C 6 cycloalkyl;

R 3 is selected from the group consisting of

(a) H;

(b) C 1 -C 3 alkyl;

(c) C 1 -C 3 alkoxy; and

(d) halo;

R 4 is selected from the group consisting of:

ring C y is a mono- or bicyclic carbocyclic ring system containing 4 to 12 carbon atoms;

ring C A is phenyl or C 3 -C 6 cycloalkyl;

R 5 is —C(O)OR A ;

R 6 is C 1 -C 3 alkyl or halo;

R 7 is H or C 1 -C 3 alkyl;

the subscript s is 0 or 1;

the subscript t is 0, 1, 2, 3, 4, or 5; and

R A is H.

2. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from the group consisting of H, methyl, and CF 3 .

3. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 3 is H or methyl.

4. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein

R 1 is H, methyl, or CF 3 ; and

R 3 is H or methyl.

5. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 4 is

6. The compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein C y is cyclobutyl, cyclohexyl, tetrahydronapthyl, or dihydroindenyl.

7. The compound of claim 6 or a pharmaceutically acceptable salt thereof, wherein

C y is cyclohexyl or tetrahydronapthyl;

R 5 is —C(O)OR A ;

R A is H;

R 6 is methyl;

the subscript s is 1; and

the subscript t is 0, 1, or 2.

8. The compound of claim 1 selected from the group consisting of:

5-hydroxy-5-{5-[4-methyl-6-(pyrazin-2-ylamino)pyridin-2-yl]-1,3-thiazol-2-yl}-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid;

4-hydroxy-2,2-dimethyl-4-{5-[4-methyl-6-(pyrazin-2-ylamino)pyridin-2-yl]-1,3-thiazol-2-yl}cyclohexanecarboxylic acid; and

1-{5-[6-(pyrazin-2-ylamino)pyridin-2-yl]-1,3-thiazol-2-yl}cyclobutanol

or a pharmaceutically acceptable salt thereof.

9. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 4 is selected from the group consisting of:

10. The compound of claim 1 , which is 5-hydroxy-5-{5-[4-methyl-6-(pyrazin-2-ylamino)pyridin-2-yl]-1,3-thiazol-2-yl}-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid, or a pharmaceutically acceptable salt thereof.

Assignments (3)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2016
From: GUAY, DANIEL; LEBRUN, MARIE-EVE; ROBICHAUD, JOEL S.
To: MERCK CANADA INC.
Reel/Frame 038264/0901 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2016
From: ANTHONY, NEVILLE J.; ANDRESEN, BRIAN M.; NORTHRUP, ALAN B.; CHILDERS, KALEEN KONRAD; DONOFRIO, ANTHONY; MILLER, THOMAS A.; LIU, YUAN; MACHACEK, MICHELLE R.; WOO, HYUN CHONG; SPENCER, KERRIE B.; ELLIS, JOHN MICHAEL; ALTMAN, MICHAEL D.; ROMEO, ERIC T.; GRIMM, JONATHAN; WANG, LIPING; DUBOIS, BYRON; DENG, QIAOLIN
To: MERCK SHARP & DOHME CORP.
Reel/Frame 038265/0162 →