反应详情

The title compound was prepared according to the general procedure for intermediate 11. 3-(4-piperidinyl)-5-(3-thienyl)-1H-indole-7-carboxamide (220 mg, 0.67 mmol) was reacted with triethyl amine (0.4 mL, 2.68 mmol) and 3-chloropropylsulfonyl chloride (0.12 mL, 1.01 mmol) to give the title compound (117 mg, 37%)

1. customThe title compound was prepared