Hydrochloric Acid → {(8R)-8-Methyl-3-{1-[4-(1,3-oxazol-2-yl)phenyl]cyclopropyl}-5,6,8,9-tetrahydro[1,2,4]triazolo[4,3-d][1,4]thiazepin-8-yl}methanol

Participants

Reaction Steps

A solution of the compound (674 mg, 1.36 mmol) obtained in Example 85-1) and 4 M hydrochloric acid (1,4-dioxane solution, 4 mL) in methanol (8 mL) was stirred overnight at room temperature. The reaction mixture was concentrated under reduced pressure, a 5 M aqueous sodium hydroxide solution (40 mL) was added to the residue, the mixture was extracted with ethyl acetate, and the organic layer was washed with saturated sodium chloride solution and dried with anhydrous sodium sulfate. After concentration under reduced pressure, the residue was purified by silica gel chromatography (ethyl acetate:methanol=20:80) to obtain the title compound (460 mg, 88%) as a yellow solid.

Provenance & Evidence