HRID387649

反应详情

EQUATION

反应方程式

HRID 387649 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

82 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-2-(2-ethoxyethyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-5-carboxamide and 1 cm3 of a 2M solution of hydrochloric acid in ethyl ether are stirred at a temperature close to 20° C., under argon. The stirring is stopped and the ethyl ether is drawn off. The paste obtained is dried under vacuum at a temperature of 40° C. 86 mg of N-[(1S,2R)-1-(3,5-difluorobenzyl)-2-hydroxy-3-({1-[3-(trifluoromethyl)phenyl]cyclopropyl}amino)propyl]-2-(2-ethoxyethyl)-1-oxo-1,2,3,4-tetrahydroisoquinoline-5-carboxamide hydrochloride (1:1) are obtained in the form of a white powder.

WORKUP

后处理

  1. customclose to 20° C., under argon
  2. customThe paste obtained
  3. customis dried under vacuum at a temperature of 40° C