1,4-Dioxane → ((+/-)-(cis)-2-Aminocyclobutyl)((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)methanone hydrochloride

Participants

Reaction Steps

A solution of tert-butyl (±)-(cis)-2-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidine-1-carbonyl)cyclobutylcarbamate (160 mg, 0.366 mmol) in 4 M HCl in dioxane (5 mL, 20.00 mmol HCl) was stirred at room temperature for 3 hours. After this time, the mixture was concentrated in vacuo, then concentrated 3× from methylene chloride to remove residual HCl and dioxane, to yield the title compound as a colorless solid which was used without purification in the next step. MS (ESI+)=327.3 (M+H)+.

Provenance & Evidence