HRID1463948

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：C[C@]12CC[C@H]3[C@@H](CC=C4NC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2C(=O)O

HCID475447

3-Oxo-4-aza-5-androstene-17beta-carboxylic acid

C19H27NO3

HCID11008278

2-(4-methoxyphenyl)propan-2-amine

C10H15NO

PRODUCTS

生成物

结构：COc1ccc(C(C)(C)NC(=O)[C@H]2CC[C@H]3[C@@H]4CC=C5NC(=O)CC[C@]5(C)[C@H]4CC[C@]23C)cc1

HCID67750660

未命名化合物

收率 65%

PROCEDURE

实验过程

The title compound was prepared in a yield of 65% in a similar manner to that described in Example 37 by reacting 3-oxo-4-azaandrost-5-ene-17β-carboxylic acid and 1-(4-methoxyphenyl)-1-methylethylamine.