反应 #2507902

反应方程式

3-methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)aniline

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

→

title compound

收率 98.0%

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

收率 98.0%

反应条件

实验过程

Acylation of 3-methoxy-4-(2-(tetrahydrofuran-2-yl)ethoxy)aniline from step A with 4-(4-chlorophenyl)-1H-pyrrole-2-carboxylic acid to generate the title compound in 98% yield was achieved via the procedure described in step C of Example 1. The crude product was used for next step without further purification.

来源