HRID445193

反应详情

EQUATION

反应方程式

HRID 445193 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

To a 500 mL three-necked round-bottom flask was added 8-benzyloxy-5-[(R)-2-bromo-1-(tert-butyldimethylsilanyloxy)ethyl]-1H-quinolin-2-one (43 g, 0.124 mol, about 95% chiral purity), 1-methyl-2-pyrrolidinone (210 mL) and benzylamine (28.3 g, 0.37 mol). The resulting mixture was flushed with nitrogen and then stirred at 90° C. for 6 hours. The mixture was then cooled to room temperature and water (300 mL) and ethyl acetate (300 mL) were added. The layers were separated and the organic layer was washed with water (200 mL), a 1:1 mixture of water and aqueous saturated sodium chloride solution (200 mL), and water (200 mL). The organic layer was then dried over magnesium sulfate, filtered and concentrated under reduced pressure to provide the title compound as an orange oil.

WORKUP

后处理

  1. customThe resulting mixture was flushed with nitrogen
  2. temperatureThe mixture was then cooled to room temperature
  3. additionwater (300 mL) and ethyl acetate (300 mL) were added
  4. customThe layers were separated
  5. washthe organic layer was washed with water (200 mL)
  6. additiona 1:1 mixture of water and aqueous saturated sodium chloride solution (200 mL), and water (200 mL)
  7. dry with materialThe organic layer was then dried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure