HRID8899

反应详情

EQUATION

反应方程式

HRID 8899 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of 2-[[6-methoxy-3-pyridinyl]methyl]amino-N-[4-(1-propynyl)-3-(trifluoromethyl)-phenyl]benzamide (step 4.1; 1.10 g, 2.5 mmol) and trimethylsilyl iodide (Fluka, Buchs, Switzerland; 1.0 mL, 7.5 mmol) in chloroform (30 mL) is stirred at 60° C. for 16 hours under an argon atmosphere. The cooled mixture is then treated with methanol (2 mL) and stirred at room temperature for 10 minutes. The solvent is evaporated under reduced pressure and the residue is treated with an aqueous solution of ammonia (100 mL of 5%) and extracted with ethyl acetate (3×100 mL). The combined extracts are washed with saturated aqueous sodium chloride (50 mL), dried (MgSO4), filtered and the solvent is evaporated under reduced pressure to yield the crude product which is purified by column chromatography on silica gel, eluent ethyl acetate and recrystallised from hot ethyl acetate hexane to give the title compound as a colourless crystalline solid; m.p. 208–212° C.

WORKUP

后处理

  1. stirringstirred at room temperature for 10 minutes
  2. customThe solvent is evaporated under reduced pressure
  3. additionthe residue is treated with an aqueous solution of ammonia (100 mL of 5%)
  4. extractionextracted with ethyl acetate (3×100 mL)
  5. washThe combined extracts are washed with saturated aqueous sodium chloride (50 mL)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customthe solvent is evaporated under reduced pressure
  9. customto yield the crude product which
  10. customis purified by column chromatography on silica gel, eluent ethyl acetate
  11. customrecrystallised from hot ethyl acetate hexane