HRID428139

反应详情

EQUATION

反应方程式

HRID 428139 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Dichloromethane (50 ml) and triethylamine (2.69 ml, 19.30 mmol) were sequentially added to trans-3-(3-pyridyl)acrylic acid (1.44 g, 9.65 mmol) and stirred for 10 minutes. Then, pivaloyl chloride (1.18 ml, 9.65 mmol) was added and stirred for 13 minutes. 1-(3,4-Dimethoxyphenyl)-2-(methylamino)ethanone hydrobromide (2.79 g, 9.65 mmol) was dissolved in dichloromethane (4 ml) and triethylamine (1.34 ml, 9.65 mmol), added to the reaction mixture and stirred at room temperature for 30 minutes. After the reaction mixture was washed with water and aqueous saturated sodium bicarbonate solution, the organic phase was dried over magnesium sulfate and the solvent was distilled out under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane:methanol=10:1) to yield a crude product. The crude product was recrystallized to yield the titled compound (1.84 g, 5.41 mmol, 56%).

WORKUP

后处理

  1. stirringstirred for 13 minutes
  2. stirringstirred at room temperature for 30 minutes
  3. washAfter the reaction mixture was washed with water and aqueous saturated sodium bicarbonate solution
  4. dry with materialthe organic phase was dried over magnesium sulfate
  5. distillationthe solvent was distilled out under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (dichloromethane:methanol=10:1)
  7. customto yield a crude product
  8. customThe crude product was recrystallized