HRID914274

反应详情

EQUATION

反应方程式

HRID 914274 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A solution of 4-{2-[(3-bromomethylbenzofuran-2-carbonyl)amino]ethoxy}-benzoic acid methyl ester (0.340 mol) in chlorobenzene (200 ml) and dichloromethane (800 ml) was added dropwise to a 0-5° C. solution of 2M dimethylamine in tetrahydrofuran (510 ml, 1.022 mol) over 30 minutes with the temperature below 20° C. The resulting mixture was stirred for one hour and allowed to warm to ambient temperature. After completion of reaction, the reaction mixture was washed with 5% potassium carbonate and water. Solvent was distilled at atmospheric pressure until the pot temperature reached 100° C. After cooling to ˜50° C., acetonitrile (400 ml) and ethyl Acetate (400 ml) were added to the pot. The reaction mixture was heated to reflux until all solids dissolved. The reaction mixture was allowed to cool to give 4-{2-[(3-dimethylaminomethyl-benzofuran-2-carbonyl)amino]ethoxy}benzoic acid methyl ester (76.6 g) as an off white powder.

WORKUP

后处理

  1. customAfter completion of reaction
  2. washthe reaction mixture was washed with 5% potassium carbonate and water
  3. distillationSolvent was distilled at atmospheric pressure until the pot temperature
  4. customreached 100° C
  5. temperatureAfter cooling to ˜50° C.
  6. additionacetonitrile (400 ml) and ethyl Acetate (400 ml) were added to the pot
  7. temperatureThe reaction mixture was heated
  8. temperatureto reflux until all solids
  9. dissolutiondissolved
  10. temperatureto cool