Aminopyrimidines as Syk inhibitors
View Patent ↗The present invention provides novel pyrimidine amines of formula (I) which are potent inhibitors of spleen tyrosine kinase, and are useful in the treatment and prevention of diseases mediated by said enzyme, such as asthma, COPD and rheumatoid arthritis.
1. A compound of formula (I) or a pharmaceutically acceptable salt thereof,
wherein
R 1 is selected from the group consisting of (a) hydrogen, (b) halogen, (c) CN, (d) C 1-6 alkyl optionally substituted with one or more groups independently selected from the group consisting of OR a and halogen, (e) C 2-6 alkenyl, (f) C 2-6 alkynyl, (g) C 3-6 cycloalkyl, (h) OH, (i) —O—C 1-6 alkyl optionally substituted with one or more groups independently selected from (i) aryl, (ii) 5- or 6-membered heteroaryl optionally substituted with one or more groups independently selected from C 1-6 alkyl, (iii) 4- to 8-membered heterocyclyl optionally substituted with one or more groups independently selected from oxo, halogen, C 1-6 alkyl, (iv) —CO 2 R a , (v) —CONR b R c , (vi) —NR b R c , (vii) —NH-heterocycle optionally substituted with alkyl, and (viii) —OR a , (j) —O—X, wherein X is selected from the group consisting of (i) 4- to 8-membered heterocyclyl optionally substituted with one or more groups independently selected from halogen, C 1-6 alkyl, —C 1-6 haloalkyl, COR a , CO 2 R a , and (ii) C 3-6 cycloalkyl optionally substituted with one or more groups independently selected from C 1-6 alkyl, —OR a , benzyl, —CO 2 R a , and —NR b R c , (k) —S(O) n —C 1-6 alkyl optionally substituted with OR a , (l) —CO 2 R a , (m) —CONR b R c , and (n) —COR a ;
R 2 is selected from the group consisting of (a) H, (b) halogen, (c) C 1-6 alkyl, (d) O—C 1-6 alkyl, (e) C 1-6 haloalkyl and (f) O—C 1-6 haloalkyl;
R 3a and R 3b are independently selected from the group consisting of (a) H, (b) C 1-8 alkyl optionally substituted with one or more groups independently selected from (i) OR a , (ii) heteroaryl optionally substituted with C 1-4 alkyl, aryl, (iii) aryl optionally substituted with halogen, C 1-4 alkyl (optionally substituted with halogen, CO 2 R a , NR b R c ), CO 2 R a , OR a , NR b R c , heteroaryl, (iv) NR b R c , (v) halogen, (vi) heterocyclyl optionally substituted with oxo, C 1-4 alkyl, OR a , NR b R c , (vii) SR a , (viii) C 3-8 cycloalkyl optionally substituted with OR a , NR b R c , and (ix) CO 2 R a , (c) heterocycle optionally substituted with one or more groups independently selected from OR a , (d) C 3-8 cycloalkyl optionally substituted with one or more groups independently selected from OR a , (e) C 3-6 alkenyl, (f) heteroaryl optionally substituted with one or more groups independently selected from C 1-4 alkyl optionally substituted with NR b R c , (g) —SO 2 R a , (h) —C(O)CH 2 OC(O)R a , (i) —C(O)R a , (j) —CO 2 R a , (k) —CONR b R c , (l) aryl optionally substituted with CO 2 R a , or
R 3a , R 3b and the nitrogen atom to which they are both attached together form a 3- to 8-membered heterocyclic ring having 0-1 additional heteroatom selected from N—R x , O and S;
wherein said ring is optionally substituted with one or more groups independently selected from (a) oxo, (b) C 1-4 alkyl optionally substituted with (i) OR a , (ii) NR b R c , (iii) NHC(O)R a , (iv) NHCO 2 R a , (v) halogen, (vi) CO 2 R a , (vii) CONR b R c , and (viii) heteroaryl, (c) OR a , (d) heteroaryl optionally substituted with aryl, C 1-4 alkyl, (e) halogen, (f) aryl optionally substituted with halogen, SO 2 R a , (g) —OCH 2 C(O)NHR b , (h) NR b R c , (i) —C(O)NR b R c , (j) —CO 2 R a , or two substituents (including R x ) on adjacent ring atoms together with said atoms form a benzene, a C 3-8 cycloalkyl, a 3- to 8-membered heterocycle, or a 5- or 6-membered heteroaryl, each optionally substituted with R x ; or two substituents on the same ring atom together with said atom form a C 3-8 cycloalkyl or a 3- to 8-membered heterocycle, each optionally substituted with R x ; or
R 3a , R 3b and the nitrogen atom to which they are both attached together form a 3- to 8-membered heteroaryl ring having 0-2 additional N, or 0-1 additional N, and 0-1 heteroatom selected from O and S;
R 4 is selected from the group consisting of (a) H, (b) halogen, (c) C 1-6 alkyl, (d) O—C 1-6 alkyl, (e) C 1-6 haloalkyl, (f) O—C 1-6 haloalkyl, (g) OH, (i) NO 2 , (j) —NR b R c , (k) NHC(O)R a , (l) NHC(O)NHR b , (m) NHC(O)NHC(O)NR b R c , (n) C 2-6 alkenyl, (o) C 2-6 alkynyl, (p) C 3-6 cycloalkyl and (q) O-benzyl,
R 5 is selected from the group consisting of H, halogen and C 1-3 alkyl;
R a is selected from the group consisting of (a) H, (b) C 1-6 alkyl optionally substituted with one or more groups independently selected from (i) halogen, (ii) CN, (iii) OH, (iv) —NR b R c , (v) heterocyclyl optionally substituted with oxo, and (vi) CO 2 H; and (c) benzyl, R b and R c are independently selected from the group consisting of H, C 1-6 alkyl and C 3-6 cycloalkyl; or
R b , R c and the nitrogen atom to which they are attached together form a 5- or 6-membered heterocycle having 0 or 1 additional heteroatom selected from O, S and N—R x , and optionally substituted with one or more groups independently selected from oxo,
R x is selected from (a) H, (b) —C(O)C 1-4 alkyl optionally substituted with OH or OC 1-4 alkyl, (c) —CO 2 C 1-4 alkyl, (d) —CO 2 C 3-4 alkenyl, (e) C(O)-heteroaryl, (f) benzyl, (g) C 1-4 alkyl optionally substituted with OH, and (h) aryl optionally substituted with CO 2 H.
2. A compound of claim 1 having the formula (Ia) or a pharmaceutically acceptable salt thereof:
wherein R 1 , R 2 , R 3a , R 3b , R 4 and R 5 are as defined in claim 1 .
3. A compound of claim 2 or a pharmaceutically acceptable salt thereof, wherein R 3a and R 3b are independently selected from (a) H, (b) C 1-6 alkyl optionally substituted with one or two groups independently selected from (i) OR a , (ii) phenyl optionally substituted with OR a , C 1-3 alkyl or CF 3 , (iii) 5- or 6-membered heterocyclyl optionally substituted with one or two groups selected from oxo, C 1-3 alkyl, OR a and NR b R c , (iv) 5- or 6-membered heteroaryl optionally substituted with one or two methyl groups, (v) C 3-6 cycloalkyl, (vi) CO 2 H, (vii) NR b R c , and (viii) SR a , (c) C 1-6 haloalkyl optionally substituted with OH, (d) C 3-6 cycloalkyl optionally substituted with OH, and (e) phenyl optionally substituted with CO 2 H or CO 2 C 1-4 alkyl.
4. A compound of claim 3 or a pharmaceutically acceptable salt thereof, wherein R 3a is H and R 3b is selected from (a) C 1-6 alkyl optionally substituted with one or two groups independently selected from (i) OR a , (ii) phenyl optionally substituted with OR a , C 1-3 alkyl or CF 3 , (iii) 5- or 6-membered heterocyclyl optionally substituted with one or two groups selected from oxo, C 1-3 alkyl, OR a and NR b R c , (iv) 5- or 6-membered heteroaryl optionally substituted with one or two methyl groups, (v) C 3-6 cycloalkyl, (vi) CO 2 H, (vii) NR b R c , and (viii) SR a , and (b) C 1-6 haloalkyl optionally substituted with OH.
5. A compound of claim 2 or a pharmaceutically acceptable salt thereof, wherein R 3a , R 3b and the nitrogen atom to which they are both attached together form a 5- or 6-membered heterocyclic ring having 0-1 additional heteroatom selected from N—R x and O, wherein said ring is optionally substituted with one or two groups independently selected from (a) oxo, (b) C 1-3 alkyl optionally substituted with OH, CO 2 H, CONH 2 , or NHCOCH 3 , (c) CF 3 , (d) OH, (e) CONH 2 , (f) CO 2 H, and (g) NH 2 .
6. A compound of claim 5 or a pharmaceutically acceptable salt thereof, wherein R 3a , R 3b and the nitrogen atom to which they are both attached together form a pyrrolidinyl or piperidinyl ring, each being optionally substituted with one or two groups independently selected from (a) oxo, (b) C 1-3 alkyl optionally substituted with OH, CO 2 H, CONH 2 , or NHCOCH 3 , (c) CF 3 , (d) OH, (e) CONH 2 , (f) CO 2 H, and (g) NH 2 .
7. A compound of claim 1 or a pharmaceutically acceptable salt thereof, having the formula (Ib) or a pharmaceutically acceptable salt thereof:
wherein R 1 , R 4 and R x are as defined in claim 1 .
8. A compound of claim 7 or a pharmaceutically acceptable salt thereof, wherein R x is H.
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.
10. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein R 1 is trifluoromethyl.
11. The compound of claim 2 or a pharmaceutically acceptable salt thereof, wherein R 1 is trifluoromethyl.
12. The compound of claim 7 or a pharmaceutically acceptable salt thereof, wherein R 1 is trifluoromethyl.
13. The compound of claim 1 or a pharmaceutically acceptable salt thereof, wherein the compound is 4-[5-(3-methyl-5-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}phenyl)-1,3-thiazol-2-yl]-1,4-diazepan-2-one.