HRID1349476

反应详情

EQUATION

反应方程式

HRID 1349476 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

To a solution of 5-benzyloxy-6-(3-chlorobenzylcarbamoyl)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid (50 mg) in dimethylformamide (0.3 ml) were added triethylamine (0.07 ml) and diphenylphosphoryl azide (0.054 ml). After stirring at room temperature for 1 hr, tert-butanol (0.3 ml) was added, and the mixture was heated to 100° C. and stirred for 1 hr. After cooling to room temperature, saturated aqueous ammonium chloride solution (5 ml) and water (5 ml) were added, and the mixture was extracted twice with ethyl acetate (15 ml each). The ethyl acetate layer was washed with water, dried and concentrated. The obtained-residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2) to give tert-butyl [5-benzyloxy-6-(3-chlorobenzylcarbamoyl)-1-(2,2-dimethoxyethyl)-4-oxo-1,4-dihydropyridin-3-yl]carbamate (40 mg).

WORKUP

后处理

  1. temperaturethe mixture was heated to 100° C.
  2. stirringstirred for 1 hr
  3. temperatureAfter cooling to room temperature
  4. extractionthe mixture was extracted twice with ethyl acetate (15 ml each)
  5. washThe ethyl acetate layer was washed with water
  6. customdried
  7. concentrationconcentrated
  8. customThe obtained-residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:2)