Synthesis of isofagomine, a novel glycosidase inhibitor

Abstract

(3R, 4R, 5R)-3,4-Dihydroxy-5-hydroxymethyl-piperidine (Isofagomine, 1) a potent β-glucosidase inhibitor was synthesised in a 6 step synthesis in an overall yield of 34% starting from 1,6:2,3-dianhydro-4- O-benzyl-β- d-mannopyranose (7). A hydroxymethyl group was introduced at C-2 in 7 by epoxide opening with vinylmagnesium bromide followed by ozonolysis with reductive workup to give 1,6-anhydro-4- O- benzyl-2-deoxy-2- C-hydroxymethyl-β- d-glucopyranose, 9. Hydrolysis of the anhydro bond and subsequent oxidative carbon chain cleavage gave a pentodialdose, which was cyclised by reductive amination with ammonia affording the 4- O-benzyl derivative of 1. After the removing the protecting group by hydrogenation under acidic conditions 1 was isolated as its hydrochloride. Synthesis of 1 was also attempted from its lactam precursur. For this purpose 5-amino-2,3-anhydro-5-deoxy-4- O- tert-butyl-dimethylsily- d-lyxono-1,5-lactam 6 was synthesised in the 5 steps from d-galactose. However, epoxide opening of 6 or 7 with the α-alkoxy cuprate dilithium benzoxymethyl-2-thienylcyanocuprate was unsuccessful.