6-substituted 2-(benzimidazolyl)purine and purinone derivatives for immunosuppression

1. A compound of formula I or II

wherein

Q is selected from the group consisting of CX and nitrogen;

X is selected from the group consisting of hydrogen, halogen, and an electron-withdrawing group;

A is chosen from the group consisting of H, (C 1 -C 6 ) alkyl, heteroaryl, and aryl;

R 1 is selected from the group consisting of halogen, CN, (C 2 -C 6 ) alkyl, substituted (C 1 -C 6 ) alkyl, aryl, substituted aryl, azetidinyl, piperidinyl, piperazinyl, pyridinyl, pyrimidinyl, morpholinyl, thiomorpholinyl, pyrrolyl, pyrazolyl, indolyl, isoquinolinyl, azepinyl, diazepinyl, cyclobutyl, substituted azetidinyl, substituted piperidinyl, substituted piperazinyl, substituted pyridinyl, substituted pyrimidinyl, substituted morpholinyl, substituted thiomorpholinyl, substituted pyrrolyl, substituted pyrazolyl, substituted indolyl, substituted isoquinolinyl, substituted azepinyl, substituted diazepinyl, substituted cyclobutyl, and —V—R 7 ;

R 2 and R 3 are selected independently for each occurrence of (CR 2 R 3 ) from the group consisting of hydrogen and (C 1 -C 6 ) alkyl;

R 4 is selected from a group consisting of alkyl, OH, alkoxy, pyranyl, benzopyranyl, furanyl, pyridinyl, cyclohexyl, aryl, substituted alkyl, substituted pyranyl, substituted benzopyranyl, substituted furanyl, substituted pyridinyl, substituted cyclohexyl, and substituted aryl;

R 7 is chosen from H, (C 1 -C 6 ) alkyl, substituted (C 1 -C 6 ) alkyl, aryl, substituted aryl, pyridinyl, piperidinyl, furanyl, oxadiazolyl, azetidinyl, cyclopropyl, cyclobutyl, cyclopentyl, and substituted pyridinyl, substituted piperidinyl, substituted furanyl, substituted oxadiazolyl, substituted azetidinyl, substituted cyclopropyl, substituted cyclobutyl, substituted cyclopentyl;

V is chosen from —C(═O)O—, —C(═O)NR 8 —, —O—, and —NR 8 —;

R 8 is chosen from H and (C 1 -C 6 ) alkyl, or, azetidinyl, piperidinyl, oxadiazolyl, cyclopropyl, cyclobutyl, cyclopentyl, substituted azetidinyl, substituted piperidinyl, substituted oxadiazolyl, substituted cyclopropyl, substituted cyclobutyl, substituted cyclopentyl;

R 9 is chosen from hydrogen, alkyl, and substituted alkyl; and

y is zero or an integer selected from 1, 2, and 3.

2. A compound according to claim 1 , wherein R 9 is hydrogen and R 1 is chosen from aryl, substituted aryl, azetidinyl, piperidinyl, piperazinyl, pyridinyl, pyrimidinyl, morpholinyl, thiomorpholinyl, pyrrolyl, pyrazolyl, indolyl, isoquinolinyl, azepinyl, diazepinyl, cyclobutyl, and substituted azetidinyl, substituted piperidinyl, substituted piperazinyl, substituted pyridinyl, substituted pyrimidinyl, substituted morpholinyl, substituted thiomorpholinyl, substituted pyrrolyl, substituted pyrazolyl, substituted indolyl, substituted isoquinolinyl, substituted azepinyl, substituted diazepinyl, substituted cyclobutyl.

3. A compound according to claim 2 , wherein R 1 is chosen from pyridinyl, pyrazolyl, pyrimidinyl, isoquinolinyl, azetidinyl, piperidinyl, piperizinyl, pyrrolidinyl, morpholinyl, azepanyl, diazepanyl, and phenyl optionally substituted with hydroxy, halogen, carboxamido, alkyl, carboxy, sulfone, alkoxy, and cyano.

4. A compound according to claim 1 , wherein R 1 is chosen from aryl, substituted aryl, (C 1 -C 6 ) alkyl, and substituted (C 1 -C 6 ) alkyl.

5. A compound according to claim 1 , wherein R 1 is —V—R 7 .

6. A compound according to claim 5 , wherein V is —C(═O)O— or —C(═O)NR 8 —, and R 7 is chosen from —CH 2 CN, (C 1 -C 6 ) alkyl, and H, or VR 7 is

7. A compound according to claim 5 , wherein V is chosen from —O— and —NR 8 —; R 7 is (C 1 -C 6 ) alkyl; and R 8 is H.

8. A compound according to claim 1 , wherein R 9 is hydrogen, y is zero and R 4 is a residue selected from a monocycle, a bicycle, a substituted monocycle, and a substituted bicycle said residue containing at least one oxygen atom.

9. A compound according to claim 8 , wherein R 4 is chosen from pyranyl, benzopyranyl, furanyl, substituted pyranyl, substituted benzopyranyl, substituted furanyl, a hydroxyl-substituted cycloalkyl, an alkoxy-substituted aryl, and a hydroxyl-substituted aryl.

10. A compound according to claim 9 , wherein R 4 is chosen from

wherein R 6 is hydrogen or fluorine, and the carbon marked with an asterisk is of the R absolute configuration.

11. A compound according to claim 1 , wherein R 9 is hydrogen, y is 1-3, R 2 and R 3 are hydrogen in all occurrences, and R 4 is alkoxy or OH of formula Ib or IIb:

wherein R 5 is hydrogen or (C 1 -C 6 ) alkyl.

12. A compound according to claim 1 , wherein R 9 is hydrogen, Q is CX, and y is zero of formula Ic or IIc:

13. A compound according to claim 12 , wherein R 1 is chosen from halogen, substituted (C 1 -C 6 ) alkyl, azetidinyl, piperidinyl, piperazinyl, pyridinyl, pyrimidinyl, morpholinyl, thiomorpholinyl, pyrrolyl, pyrazolyl, indolyl, isoquinolinyl, azepinyl, diazepinyl, cyclobutyl, substituted azetidinyl, substituted piperidinyl, substituted piperazinyl, substituted pyridinyl, substituted pyrimidinyl, substituted morpholinyl, substituted thiomorpholinyl, substituted pyrrolyl, substituted pyrazolyl, substituted indolyl, substituted isoquinolinyl, substituted azepinyl, substituted diazepinyl, substituted cyclobutyl, aryl, substituted aryl, and —V—R 7 .

14. A compound according to claim 13 , wherein

V is —NR 8 —, —C(═O)O—, —C(═O)NR 8 , or O;

R 7 is H, (C 1 -C 6 ) alkyl, substituted (C 1 -C 6 ) alkyl, pyridinyl, piperidinyl, furanyl, oxadiazolyl, azetidinyl, cyclopropyl, cyclobutyl, cyclopentyl, substituted pyridinyl, substituted piperidinyl, substituted furanyl, substituted oxadiazolyl, substituted azetidinyl, substituted cyclopropyl, substituted cyclobutyl, substituted cyclopentyl, or aryl; and

R 8 is hydrogen or (C 1 -C 6 ) alkyl, or azetidinyl, piperidinyl, oxadiazolyl, cyclopropyl, cyclobutyl, cyclopentyl, substituted azetidinyl, substituted piperidinyl, substituted oxadiazolyl, substituted cyclopropyl, substituted cyclobutyl, substituted cyclopentyl.

15. A compound according to claim 12 , wherein

R 4 is chosen from tetrahydrofuranyl, pyranyl, benzopyranyl, hydroxytetralinyl, oxepanyl, hydroxycyclohexyl, and their halogenated congeners;

R 1 is chosen from halogen, (C 2 -C 6 ) alkyl, substituted (C 1 -C 6 ) alkyl, azetidinyl, phenyl, piperidinyl, piperizinyl, pyrrolidinyl, morpholinyl, azepanyl, diazepanyl, pyridinyl, pyrimidinyl, and pyrazolyl optionally substituted with hydroxy, halogen, carboxamido, alkyl, carboxy, sulfonyl, alkoxy, and cyano; and

X is chosen from halogen, cyano, substituted alkoxy, and hydrogen.

16. A compound according to claim 15 selected from the group consisting of:

17. A compound according to claim 14 selected from the group consisting of:

18. A compound according to claim 1 , wherein R 9 is hydrogen, Q is CX, y is zero, and R 4 is hydroxytetralinyl and hydroxycyclohexyl of formula Id or IId:

wherein R 6 is H or halogen, and R 1 is chosen from halogen, azetidinyl, piperidinyl, piperizinyl, pyrrolidinyl, phenyl, morpholinyl, azepanyl, diazepanyl, pyridinyl pyrimidinyl, and pyrazolyl optionally substituted with hydroxy, halogen, carboxamido, alkyl, carboxy, sulfonyl, alkoxy, and cyano; and X is halogen, cyano, substituted alkoxy, and hydrogen.

19. A compound according to claim 18 selected from

20. A compound according to claim 1 , wherein Q is CX, y is zero, and R 9 is alkyl or substituted alkyl of formula Ie:

21. A compound according to claim 20 , wherein R 4 is chosen from tetrahydrofuran, benzopyran, hydroxytetralin, oxepane, hydroxycyclohexane, and their halogenated congeners.

22. A compound according to claim 21 , wherein R 1 is chosen from halogen, heteroaryl, heterocyclyl, substituted (C 1 -C 6 ) alkyl, aryl, substituted aryl, cyano, carboxy, carboalkoxy, carboxamido, and amidino; and X is chosen from halogen, cyano, hydrogen, or alkoxy.

23. A compound according to claim 22 selected from the group consisting of:

24. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of a compound according to claim 1 .