Synthesis of epothilones, intermediates thereto, analogues and uses thereof
View Patent ↗The present invention provides convergent processes for preparing epothilone A and B, desoxyepothilones A and B, and analogues thereof. Also provided are analogues related to epothilone A and B and intermediates useful for preparing same. The present invention further provides novel compositions based on analogues of the epothilones and methods for the treatment of cancer and cancer which has developed a multidrug-resistant phenotype.
1. A method of preparing an epothilone precursor having the structure:
wherein R 1 is hydrogen or methyl; wherein X is O, or a hydrogen and OR″, each singly bonded to carbon; and wherein R 0 , R′ and R″ are independently hydrogen, a linear or branched alkyl, substituted or unsubstituted aryl or benzyl, trialkylsilyl, dialkylarylsilyl, alkyldiarylsilyl, a linear or branched acyl, substituted or unsubstituted aroyl or benzoyl, which comprises
(a) coupling a compound having the structure:
wherein R is an acetyl, with an aldehyde having the structure:
wherein Y is oxygen, under suitable conditions to form an aldol intermediate and optionally protecting the aldol intermediate under suitable conditions to form an acyclic epothilone precursor having the structure:
(b) subjecting the acyclic epothilone precursor to conditions leading to intramolecular olefin metathesis to form the epothilone precursor.
2. The method of claim 1 wherein the conditions leading to intramolecular olefin metathesis require the presence of an organometallic catalyst.
3. The method of claim 1 wherein the catalyst is a Ru or Mo complex.
4. A method of preparing a protected epothilone having the structure:
wherein R 1 is hydroaen or methyl; and
R′ and R″ are independently hydrogen, a linear or branched alkyl, substituted or unsubstituted aryl or benzyl, trialkylsilyl, dialkyl-arylsilyl, alkyldiarylsilyl, a linear or branched acyl, substituted or unsubstituted aroyl or benzoyl, which comprises:
(a) monoprotecting a cyclic dial having the structure:
under suitable conditions to form a cyclic alcohol having the structure:
and
(b) oxidizing the cyclic alcohol formed in step (a) under suitable conditions to form the protected epothilone.
5. The method of claim 4 wherein R′ and R″ are TBS.
6. The method of claim 1 , wherein step (a) comprises using a non-nucleophilic base.
7. The method of claim 6 , wherein the non-nucleophilic base is lithium diethylamide or lithium diisopropylamide.
8. The method of claim 1 , wherein step (a) is performed at subambient temperatures.
9. The method of claim 1 , wherein step (a) is performed at about −78° C.
10. The method of claim 2 , wherein the catalyst is Grubbs's catalyst.
11. The method of claim 4 , wherein step (a) is performed in the presence of a base.
12. The method of claim 11 , wherein the base is 2,6-lutidine.
13. The method of claim 4 , wherein step (a) is performed in an inert organic solvent.
14. The method of claim 13 , wherein the solvent is dichloromethane.
15. The method of claim 4 , wherein step (a) is performed at subambient temperatures.
16. The method of claim 4 , wherein step (a) is performed at about −30° C.
17. The method of claim 4 , wherein step (b) is performed using Dess-Martin periodinane in an inert organic solvent.
18. The method of claim 17 , wherein the solvent is dichloromethane.
19. The method of claim 4 , wherein step (b) is performed at 20-25° C.