IP Library Granted Patent US 7,514,409
Granted Patent B2
US 7,514,409 · App. 10/591,820 · Granted Apr 7, 2009

VLA-4 antagonists

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Quick Facts
Patent No.
US 7,514,409
App. No.
10/591,820
Granted
Apr 7, 2009
Kind
B2
Abstract

Compounds of Formula I are antagonists of VLA-4, and as such are useful in the inhibition or prevention of cell adhesion and cell-adhesion mediated pathologies. These compounds may be formulated into pharmaceutical compositions and are suitable for use in the treatment of inflammatory bowel disease including ulcerative colitis and Crohn's disease, multiple sclerosis, asthma, and rheumatoid arthritis.

Claims (29)

1. A compound of formula I:

or a pharmaceutically acceptable salt thereof, wherein:

A is N or N + —O − ;

X and Y are independently selected from halogen, C 1-3 alkyl, and C 1-3 alkoxy;

R 1 is selected from (1) hydrogen, (2) C 1-10 alkyl, (3) —(C 1-10 alkyl)-aryl, (4) —(C 1-10 alkyl)-O—C 1-10 alkyl, (5) —(C 1-10 alkyl)-OC(O)—C 1-10 alkyl, (6) —(C 1-10 alkyl)-OC(O)-aryl, (7) —(C 1-10 alkyl)-OC(O)O—C 1-10 alkyl and (8) —(C 1-10 alkyl)N + (C 1-3 alkyl) 3 ; wherein alkyl is optionally substituted with one to three substituents independently selected from R a , and aryl is optionally substituted with one to three substituents independently selected from R b ;

R 2 is hydrogen or methyl;

R 3 and R 4 are independently selected from (1) hydrogen, (2) —NR d R e , (3) —NR d S(O) m R e , (4) —NR d C(O)R e , (5) —NR d C(O)OR e , and (6) —NR d C(O)NR d R e , with the proviso that R 3 and R 4 are not both hydrogen;

R a is selected from (1) —OR d , (2) —NR d S(O) m R e , (3) —NO 2 , (4) halogen, (5) —S(O) m R d , (6) —SR d , (7) —S(O) 2 OR d , (8) —S(O) m NR d R e , (9) —NR d R e , (10) —O(CR f R g ) n NR d R e , (11) —C(O)R d , (12) —CO 2 R d , (13) —CO 2 (CR f R g ) n CONR d R e , (14) —OC(O)R d , (15) —CN, (16) —C(O)NR d R e , (17) —NR d C(O)R e , (18) —OC(O)NR d R e , (19) —NR d C(O)OR e , (20) —NR d C(O)NR d R e , (21) —CR d (N—OR e ), (22) CF 3 , (23) —OCF 3 , (24) C 3-8 cycloalkyl, and (25) heterocyclyl; wherein cycloalkyl and heterocyclyl are optionally substituted with one to three groups independently selected from R c ;

R b is selected from (1) a group selected from R a , (2) C 1-10 alkyl, (3) C 2-10 alkenyl (4) C 2-10 alkynyl, (5) aryl, and (6) —(C 1-10 alkyl)-aryl, wherein alkyl, alkenyl, alkynyl, and aryl are optionally substituted with one to three substituents selected from a group independently selected from R c ;

R c is (1) halogen, (2) amino, (3) carboxy, (4) C 1-4 alkyl, (5) C 1-4 alkoxy, (6) aryl, (7) —(C 1-4 alkyl)-aryl, (8) hydroxy, (9) CF 3 , (10) OC(O)C 1-4 alkyl, (11) OC(O)NR f R g , or (12) aryloxy;

R d and R e are independently selected from hydrogen, C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, Cy and —(C 1-10 alkyl)-Cy, wherein alkyl, alkenyl, alkynyl and Cy are optionally substituted with one to four substituents independently selected from R c ; or

R d and R e together with the atom(s) to which they are attached form a heterocyclic ring of 4 to 7 members containing 0-2 additional heteroatoms independently selected from O, S and N—R h , and wherein said heterocyclic ring is optionally fused with a C 3-8 carbocyclic ring or is optional substituted with 1 to 4 groups independently selected from C 1-10 alkyl;

R f and R g are independently selected from hydrogen, C 1-10 alkyl, Cy and —(C 1-10 alkyl)-Cy; or

R f and R g together with the carbon to which they are attached form a ring of 5 to 7 members containing 0-2 heteroatoms independently selected from oxygen, sulfur and nitrogen;

R h is selected from R f and —C(O)R f ;

Cy is selected from cycloalkyl, heterocyclyl, aryl, and heteroaryl; and

m is 1 or 2.

2. A compound of claim 1 wherein one of X and Y is halogen and the other is selected from halogen, C 1-3 alkyl and C 1-3 alkoxy.

3. A compound of claim 1 wherein R 1 is hydrogen, C 1-4 alkyl, —(C 1-4 alkyl)OC(O)—C 1-4 alkyl, or —(C 1-4 alkyl)OC(O)—C 1-4 alkyl.

4. A compound of claim 1 wherein R 3 is hydrogen, and R 4 is NR d R e .

5. A compound of claim 1 wherein R 3 is NR d R e and R 4 is hydrogen.

6. A compound of claim 1 having the formula Ia:

or a pharmaceutically acceptable salt thereof, wherein

A is N or N + O − ;

R 1 is selected from hydrogen, C 1-10 alkyl, —(C 1-4 alkyl)-aryl, —(C 1-4 alkyl)-O—C 1-4 alkyl, and —(C 1-4 alkyl)-OC(O)—C 1-4 alkyl;

one of R 3 and R 4 is NR d R e and the other is hydrogen.

7. A compound of claim 6 wherein R d is hydrogen and R e is t-butyl or cyclobutyl.

8. A compound of claim 6 wherein R 3 is hydrogen, and R d and R e together with the nitrogen atom to which they are attached form a heterocyclic ring of 4 to 7 members containing no additional heteroatom and optionally substituted with 1 or 2 groups independently selected from C 1-4 alkyl.

9. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.

Assignments (5)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
CHANGE OF NAME Recorded Aug 29, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028866/0511 →
MERGER Recorded Aug 27, 2012
From: MERCK SHARP & DOHME CORP.
To: SCHERING CORPORATION
Reel/Frame 028850/0515 →
CHANGE OF NAME Recorded Jan 29, 2010
From: MERCK & CO., INC.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 023870/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 7, 2007
From: HAGMANN, WILLIAM K.; LIU, PING; LIN, LINUS S.; MUMFORD, RICHARD A.; REGER, THOMAS S.; SMITH, NICHOLAS D.; STOOK, NICHOLAS; ZUNIC, JASMINE
To: MERCK & CO., INC.
Reel/Frame 018978/0393 →