HRID1587900

反应详情

EQUATION

反应方程式

HRID 1587900 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

3.5 g (0.011 mol) of 2-Benzoylamino-4-bromoacetyl-thiazole are dissolved in 20 ml of dimethylformamide and added dropwise to a stirred solution, at room temperature, of 2.6 g (0.092 mol) of N-benzyl-2-(4-carbomethoxyphenyl)-1-methylethylamine and 1.1 g (0.011 mol) of triethylamine dissolved in 40 ml of dimethylformamide. After 1.5 hours ice/water is added, and the mixture is extracted with methylene chloride. The extract is dried over sodium sulphate and concentrated. The resulting amino-ketone is taken up in 100 ml of methanol and at room temperature, 0.6 g of sodium borohydride is added. After 1 hour the mixture is evaporated to dryness, water is added, and hydrochloric acid is used to acidify. After 10 minutes the mixture is made alkaline with ammonia and extracted with methylene chloride. The extract is dried over sodium sulphate, concentrated and purified on a silica gel column using toluene/ethyl acetate=8:2 as eluant.

WORKUP

后处理

  1. extractionthe mixture is extracted with methylene chloride
  2. dry with materialThe extract is dried over sodium sulphate
  3. concentrationconcentrated
  4. customis taken up in 100 ml of methanol and at room temperature
  5. addition0.6 g of sodium borohydride is added
  6. customAfter 1 hour the mixture is evaporated to dryness, water
  7. additionis added
  8. extractionalkaline with ammonia and extracted with methylene chloride
  9. dry with materialThe extract is dried over sodium sulphate
  10. concentrationconcentrated
  11. custompurified on a silica gel column