HRID9444

反应详情

EQUATION

反应方程式

HRID 9444 的结构方程式

PROCEDURE

实验过程

7-Bromo-4-chloro-3-nitroquinoline (33.0 g, 115 mmol) was treated with 4-(2-aminoethyl)-1-(tert-butoxycarbonyl)piperazine (26.4 mL, 115 mmol) according to the method described in Part E of Example 1. The reaction was stirred overnight. The crude product was triturated with diethyl ether and isolated by filtration to provide 33.05 g of tert-butyl 4-[2-(7-bromo-3-nitroquinolin-4-ylamino)ethyl]piperazine-1-carboxylate as a yellow solid.

WORKUP

后处理

  1. customThe crude product was triturated with diethyl ether
  2. customisolated by filtration