HRID1796768

反应详情

EQUATION

反应方程式

HRID 1796768 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

The compound (6.63 g) prepared in step (a) of Example 125 was dissolved in carbon tetrachloride (200 ml). N-Chlorosuccinimide (3.47 g) and AIBN (0.66 g) were added to the solution, and the mixture was heated at 90° C. with stirring for one hr. The temperature of the reaction solution was returned to room temperature. Chloroform was then added to the reaction solution, and the mixture was washed with water, followed by drying over anhydrous MgSO4 The solvent was then removed by distillation under the reduced pressure. The residue was crudely purified by column chromatography on silica gel (ethyl acetate). The solvent was removed by distillation under the reduced pressure. Chloroform was added to the residue, and the precipitated crystal was collected by filtration (and washed with diethyl ether) to give 7-(4-tert-butoxycarbonyl-piperazin-1-yl)-8-chloro-3,4-dihydro-2H-isoquinolin-1-one (0.89 g).

WORKUP

后处理

  1. customwas returned to room temperature
  2. washthe mixture was washed with water
  3. dry with materialby drying over anhydrous MgSO4 The solvent
  4. customwas then removed by distillation under the reduced pressure
  5. customThe residue was crudely purified by column chromatography on silica gel (ethyl acetate)
  6. customThe solvent was removed by distillation under the reduced pressure
  7. additionChloroform was added to the residue
  8. filtrationthe precipitated crystal was collected by filtration (and washed with diethyl ether)