Fused heterocyclic compounds useful as kinase modulators

1. A compound according to formula (I):

or an enantiomer, diastereomer, or a pharmaceutically-acceptable salt thereof, wherein

Q is N;

Y is NR 6 R 7 , wherein R 6 and R 7 are taken together with the nitrogen atom to which they are both attached to form an optionally substituted heterocyclo or optionally substituted heteroaryl;

A is selected from NH 2 and NHCONH 2 provided D is absent;

A is selected from NH, NHCO, and NHCONH, provided D is other than absent;

A is selected from NHCOO, provided D is other than optionally substituted alkoxy or absent;

D is optionally substituted alkyl, optionally substituted alkoxy, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclo, optionally substituted heteroaryl or is absent;

R 1 is selected from hydrogen, optionally substituted C 1-4 alkyl, and cyano;

R 2 is selected from hydrogen, optionally substituted C 1-4 alkyl, amino, cyano, optionally substituted amide, and optionally substituted carboxamide; and

R 4 is selected from hydrogen, optionally substituted aryl, optionally substituted heterocyclo and optionally substituted heteroaryl.

2. A compound according to formula (II):

or an enantiomer, diastereomer, or a pharmaceutically-acceptable salt thereof, wherein

R 1 is hydrogen;

R 2 is selected from hydrogen, amino, cyano, C 1-4 alkyl optionally substituted with amino, —C(═O)NR 11 R 12 , and —NR 11 C(═O)R 12 , wherein R 11 and R 12 are each independently selected from hydrogen, C 1-4 alkyl, C 3-7 cycloalkyl, aryl, heteroaryl, and heterocyclo;

R 8 and R 9 are each independently selected from hydrogen, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted cycloalkyl, and optionally substituted heterocyclo; or R 8 and R 9 may be taken together with the nitrogen atom to which they are both attached to form an optionally substituted heterocyclo or optionally substituted heteroaryl; and

R 10 is selected from optionally substituted alkyl, optionally substituted alkoxy, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted heterocyclo and optionally substituted heteroaryl.

3. The compound according to claim 2 , wherein R 8 and R 9 are each independently selected from hydrogen, C 1-4 alkyl, heteroaryl and heterocyclo, wherein said C 1-4 alkyl, heteroaryl and heterocyclo are optionally substituted with one or more substituents selected from halogen, cyano, hydroxy, C 1-4 alkoxy, C 1-4 alkyl, haloalkyl, C 3-7 cycloalkyl, heterocyclo, —NR 13 R 14 , and —C(O)OR 13 wherein R 13 and R 14 are each independently selected from hydrogen, C 1-4 alkyl, and heterocyclo.

4. The compound according to claim 3 , wherein —NR 8 R 9 is selected from

5. The compound according to claim 2 , wherein R 8 and R 9 are taken together with the nitrogen atom to which they are both attached to form a 5- to 7-membered monocyclic heteroaryl or heterocyclo, or a 7- to 11-membered bicyclic heteroaryl or heterocyclo, wherein said heteroaryl and heterocyclo are independently optionally substituted as valence allows with one or more substituents selected from hydrogen, optionally substituted C 1-4 alkyl, optionally substituted C 2-4 alkenyl, optionally substituted C 2-4 alkynyl, halogen, hydroxy, haloalkyl, hydroxyalkyl, cyano, nitro, —O(C 1-4 alkyl), —C(═O)H, —C(═O), —S(C 1-4 alkyl), —NH 2 , —NH(C 1-4 alkyl), —N(C 1-4 alkyl) 2 , and —NH(alkylene)OR 17 wherein R 17 is selected from hydrogen and C 1-4 alkyl.

6. The compound according to claim 5 , wherein —NR 8 R 9 is selected from

7. The compound according to claim 2 , wherein

R 10 is selected from aryl, 5- to 7-membered monocyclic heteroaryl or heterocyclo, and 7- to 11-membered bicyclic heteroaryl or heterocyclo, any of which may be independently optionally substituted as valence allows with one or more substituents selected from halogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, nitro, cyano, —OR 15 , —NR 15 R 16 , —NR 15 C(═O)R 16 , —CO 2 R 15 , —C(═O)R 15 , —O—C(═O)R 15 , —C(═O)NR 15 R 16 , cycloalkyl, heterocyclo, aryl, and heteroaryl wherein said cycloalkyl, aryl, heterocyclo, and heteroaryl are independently optionally substituted as valence allows with one or more R 18 ;

R 15 and R 16 are each independently selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, cycloalkyl, aryl, heteroaryl, and heterocyclo; and

R 18 is selected from hydrogen, halogen, hydroxyl, alkoxy, alkyl, substituted alkyl, alkenyl, substituted alkenyl, cycloalkyl, aryl, heteroaryl, and heterocyclo.

8. The compound according to claim 7 , wherein

R 10 is selected from

9. The compound according to claim 2 , wherein

R 1 is hydrogen;

R 2 is selected from hydrogen, amino, cyano, C 1-4 alkyl optionally substituted with amino, —C(═O)NR 11 R 12 , and —NR 11 C(═O)R 12 , wherein R 11 and R 12 are each independently selected from hydrogen, C 1-4 alkyl, C 3-7 cycloalkyl, aryl, heteroaryl, and heterocyclo;

R 8 and R 9 are each independently selected from hydrogen, C 1-4 alkyl, heteroaryl and heterocyclo, wherein said C 1-4 alkyl, heteroaryl and heterocyclo are optionally substituted with one or more substituents selected from halogen, cyano, hydroxy, C 1-4 alkoxy, C 1-4 alkyl, haloalkyl, C 3-7 cycloalkyl, heterocyclo, —NR 13 R 14 , and —C(O)OR 13 wherein R 13 and R 14 are each independently selected from hydrogen, C 1-4 alkyl, and heterocyclo; or

R 8 and R 9 are taken together with the nitrogen atom to which they are both attached to form a 5- to 7-membered monocyclic heteroaryl or heterocyclo, or a 7- to 11-membered bicyclic heteroaryl or heterocyclo, wherein said heteroaryl and heterocyclo are independently optionally substituted as valence allows with one or more substituents selected from hydrogen, optionally substituted C 1-4 alkyl, optionally substituted C 2-4 alkenyl, optionally substituted C 2-4 alkynyl, halogen, hydroxy, haloalkyl, hydroxyalkyl, cyano, nitro, —O(C 1-4 alkyl), —C(═O)H, —C(═O), —S(C 1-4 alkyl), —NH 2 , —NH(C 1-4 alkyl), —N(C 1-4 alkyl) 2 , —NH(alkylene)OR 17 wherein R 17 is selected from hydrogen and C 1-4 alkyl;

R 10 is selected from alkoxy, aryl, 5- to 7-membered monocyclic heteroaryl or heterocyclo, and 7- to 11-membered bicyclic heteroaryl or heterocyclo, any of which may be independently optionally substituted as valence allows with one or more substituents selected from halogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, nitro, cyano, —OR 15 , —NR 15 R 16 , —NR 15 C(═O)R 16 , —CO 2 R 15 , —C(═O)R 15 ,—O—C(═O)R 15 , —C(═O)NR 15 R 16 , cycloalkyl, heterocyclo, aryl, and heteroaryl wherein said cycloalkyl, aryl, heterocyclo, and heteroaryl are independently optionally substituted as valence allows with one or more R 18 ;

R 15 and R 16 are each independently selected from hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, cycloalkyl, aryl, heteroaryl, and heterocyclo; and

R 18 is selected from hydrogen, halogen, hydroxyl, alkoxy, alkyl, substituted alkyl, alkenyl, substituted alkenyl, cycloalkyl, aryl, heteroaryl, and heterocyclo.

10. A pharmaceutical composition comprising one or more compounds according to claim 1 and a pharmaceutically acceptable carrier or diluent.

11. A method of treating rheumatoid arthritis comprising administering to a patient in need of such treatment a therapeutically-effective amount of a compound according to claim 2 .