HRID1670481

反应详情

EQUATION

反应方程式

HRID 1670481 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

298 mg. (0.92 mmol) of [3-chloro-4-(4-methyl-piperazin-1-yl)-phenyl]-carbamic acid tert-butyl ester (Example 65b) are dissolved in 5 ml of 4 N HCl in dioxane. The solution is stirred for 4 h at 50° C., and after this time water is added and the pH is adjusted to 8 with NaHCO3. The suspension is extracted with n-butanol. The organic phase is washed with water, dried over MgSO4 and evaporated to dryness to provide the title compound. Title compound: ES-MS: 226.2 (M+Hr; analytical HPLC: tret=3.09 minutes (Grad 2).

WORKUP

后处理

  1. extractionThe suspension is extracted with n-butanol
  2. washThe organic phase is washed with water
  3. dry with materialdried over MgSO4
  4. customevaporated to dryness