反应详情

Using deprotection method A, 3-chloro-N-[1-(2-pyridinyl)-2-(1-isopropylpiperidin-4-ylmethoxy)ethyl]-1H-indole-6-carboxamide (105 mg, 0.25 mmol) and acetone (1.2 mL, 16.8 mmol) afforded 110 mg (96%) of the title compound.