HRID1017435

反应详情

EQUATION

反应方程式

HRID 1017435 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
92.5 °C

PROCEDURE

实验过程

A suspension of 56 g (152 mmol) 2,2-dimethyl-N-[6-(4-methyl-piperazin-1-yl)-4-o-tolyl-pyridin-3-yl]-propionamide in 1300 ml 3 N hydrochloric acid solution was heated to 90-95° C. overnight. The reaction mixture was cooled to room temperature, washed with three 500 ml portions diethyl ether and filtered over celite. The filtrate was diluted with 500 ml water and was adjusted to pH 7-8 by addition of 28% sodium hydroxide solution under ice cooling. The product was extracted with four 1000 ml portions of dichloromethane. The combined organic layers were washed with 500 ml brine, dried (magnesium sulfate) and evaporated to give 35 g (82%) of the title compound as a light brown oil.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. washwashed with three 500 ml portions diethyl ether
  3. filtrationfiltered over celite
  4. additionThe filtrate was diluted with 500 ml water
  5. additionwas adjusted to pH 7-8 by addition of 28% sodium hydroxide solution under ice cooling
  6. extractionThe product was extracted with four 1000 ml portions of dichloromethane
  7. washThe combined organic layers were washed with 500 ml brine
  8. dry with materialdried (magnesium sulfate)
  9. customevaporated