HRID747695

反应详情

EQUATION

反应方程式

HRID 747695 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

262 mg (1.15 mmol) of methyl 4-[(pyridine-4-yl)methyl]benzoate was dissolved in 5 ml of concentrated hydrochloric acid. The solution was stirred at 70° C. for 15 hours. The solvent was evaporated, and the residue was dissolved in 5 ml of dichloromethane. 0.24 ml (1.73 mmol) of triethylamine, 243 mg (1.27 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, 172 mg (1.27 mmol) of 1-hydroxybenzotriazole and 308 mg (1.27 mmol) of 3-(2-aminoethoxy)benzonitrile hydrochloride were added to the solution, and they were stirred for 15 hours. The reaction liquid was diluted with water. After the extraction with ethyl acetate, the organic layer was successively washed with water, 1 N sodium hydroxide and saturated aqueous NaCl solution, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by the silica gel column chromatography to obtain the title compound.

WORKUP

后处理

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in 5 ml of dichloromethane
  3. stirringwere stirred for 15 hours
  4. customThe reaction liquid
  5. extractionAfter the extraction with ethyl acetate
  6. washthe organic layer was successively washed with water, 1 N sodium hydroxide and saturated aqueous NaCl solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. customThe solvent was evaporated
  9. customthe residue was purified by the silica gel column chromatography