Methanol → {1-[4-Chloro-3-(5-methyoxy-1H-benzoimidazol-2-yl)-phenyl]-pyrrolidin-4-yl}-pyrolidin-1-yl-methanone formate

Participants

Reaction Steps

Method F—Step b To a mixture of 2-{2-Chloro-5-[4-(pyrrolidine-1-carbonyl)-piperidin-1-yl]-phenyl}-5-methoxy-benzoimidazole-1-carboxylic acid tert-butyl ester (0.10 g, 0.19 mmol) in 2M HCl in Et2O (2 mL), few drops of dichloromethane and methanol were added to improve the solubility of the starting material. The resulting mixture was stirred overnight at room temperature, Et2O was added (5 mL), the precipitate was filtered off and then purified by PrepHPLC to get 0.03 g of the title compound as hydrochloride salt, with quantitative yield.

Provenance & Evidence