HRID1184103

反应详情

EQUATION

反应方程式

HRID 1184103 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
50 °C

PROCEDURE

实验过程

2-(Trichloromethyl)-1H-benzimidazole (19 g) and 1-tert-butyl 3-methyl (3R,5S)-5-[(2-methylpropyl)amino]piperidine-1,3-dicarboxylate (25 g) were dissolved in THF (1200 ml), sodium hydrogen carbonate (67 g) and water (600 ml) were added, and the mixture was stirred at room temperature for 1 hr and at 50° C. for 1 hr. After evaporation of the solvent, the residue was extracted 3 times with ethyl acetate (700 ml). The extract was washed successively with 10%-aqueous citric acid solution (500 ml) and brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in ethyl acetate (1000 ml), subjected to basic silica gel column chromatography, and a fraction eluted with ethyl acetate was concentrated under reduced pressure to give the object product (30.6 g).

WORKUP

后处理

  1. customAfter evaporation of the solvent
  2. extractionthe residue was extracted 3 times with ethyl acetate (700 ml)
  3. washThe extract was washed successively with 10%-aqueous citric acid solution (500 ml) and brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customThe solvent was evaporated under reduced pressure
  6. dissolutionThe residue was dissolved in ethyl acetate (1000 ml)
  7. washa fraction eluted with ethyl acetate
  8. concentrationwas concentrated under reduced pressure