Protein kinase C inhibitors and uses thereof
This disclosure concerns compounds which are useful as inhibitors of protein kinase C (PKC) and are thus useful for treating a variety of diseases and disorders that are mediated or sustained through the activity of PKC. This disclosure also relates to pharmaceutical compositions comprising these compounds, methods of using these compounds in the treatment of various diseases and disorders, processes for preparing these compounds and intermediates useful in these processes.
1. A method for preparing an optically active compound, comprising contacting a racemic mixture of compounds of the formula:
with a lipase; wherein
R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 are independently selected from hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminoacyl, aminoacyloxy, oxyaminoacyl, azido, cyano, halogen, hydroxyl, carboxyl, carboxylalkyl, thiol, thioalkoxy, substituted thioalkoxy, aryl, aryloxy, hydroxyamino, alkoxyamino, nitro, —SO-alkyl, —SO-substituted alkyl, —SO-aryl, —SO-heteroaryl, —SO 2 -alkyl, —SO 2 -substituted alkyl, —SO 2 -aryl and —SO 2 -heteroaryl; or R 1 and R 2 together form an oxo group; or R 3 and R 4 together form an oxo group; or R 5 and R 6 together form an oxo group; and
R 7 , R 8 , R 9 , and R 10 are independently selected from hydrogen, alkyl, substituted alkyl, alkoxy, substituted alkoxy, acyl, acylamino, acyloxy, amino, substituted amino, aminoacyl, aminoacyloxy, oxyaminoacyl, azido, cyano, halogen, hydroxyl, carboxyl, carboxylalkyl, thiol, thioalkoxy, substituted thioalkoxy, aryl, aryloxy, hydroxyamino, alkoxyamino, nitro, —SO-alkyl, —SO-substituted alkyl, —SO-aryl, —SO-heteroaryl, —SO 2 -alkyl, —SO 2 -substituted alkyl, —SO 2 -aryl and —SO 2 -heteroaryl; or R 7 and R 8 together form an oxo group; or R 9 and R 10 together form an oxo group.
2. The method of claim 1 , wherein the lipase performs enzyme-catalyzed acylation of one of the stereoisomers in the racemic mixture.
3. The method of claim 1 , further comprising after the contacting, separating a stereoisomer from the racemic mixture.
4. The method of claim 3 , wherein the separating comprising separating the stereoisomer by chromatography.
5. The method of claim 3 , wherein the separated stereoisomer comprises an acyl group.
6. The method of claim 3 , wherein the separated stereoisomer comprises a hydroxyl group.
7. The method of claim 6 , further comprising converting the hydroxyl group of the separated stereoisomer to an amino group.
8. The method of claim 7 , further comprising contacting the separated stereoisomer with a compound of the formula:
to produce a compound according to the formula:
wherein
R 11 is selected from alkyl, substituted alkyl, hydroxy, alkoxy, substituted alkoxy, amino, substituted amino, carboxyl, carboxyl ester, cyano, halogen, acyl, aminoacyl, nitro, alkenyl, substituted alkenyl, alkynyl, and substituted alkynyl; and
Y 1 is selected from hydrogen, alkyl and substituted alkyl.
9. The method of claim 8 , further comprising contacting the compound according to the formula:
with a compound of the formula HNY 2 Ar 1 to produce a compound according to the formula:
wherein
Y 2 is selected from hydrogen, alkyl and substituted alkyl; and
Ar 1 is selected from aryl, substituted aryl, heteroaryl, and substituted heteroaryl.
10. The method of claim 9 , wherein the reaction is run in a polar aprotic or polar protic solvent.
11. The method of claim 9 , further comprising performing separation of isomers with chiral chromatography.
12. The method of claim 9 , further comprising performing separation of isomers with a resolution technique.
13. The method of claim 9 , wherein Ar 1 is aryl or substituted aryl.
14. The method of claim 9 , wherein Ar 1 is heteroaryl or substituted heteroaryl.