反应 #2507889

反应方程式

4-methoxy-3-(2-(pyrrolidin-1-yl)ethoxy)benzenamine

4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid

→

title compound

收率 74.0%

4-(4-chlorophenyl)-N-(4-methoxy-3-(2-(pyrrolidin-1-yl)ethoxy)phenyl)-1H-pyrrole-2-carboxamide

收率 74.0%

反应条件

实验过程

Acylation of 4-methoxy-3-(2-(pyrrolidin-1-yl)ethoxy)benzenamine from step A with 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid to generate the title compound in 74% yield was achieved via the procedure described in step C of Example 1. MS (ESI) 440 (M+H)+.

来源