HRID569342

反应详情

EQUATION

反应方程式

HRID 569342 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

Vilsmeir reagent, which was prepared from N,N-dimethylformamide (0.48 g) and phosphorus oxychloride (1.0 g), was suspended in ethyl acetate (20 ml), and thereto was added 4-bromo-2-methoxyiminoacetoacetic acid (syn isomer) (1.34 g) under ice-cooling, followed by stirring at the same temperature for half an hour to prepare the activated acid solution. This solution was added to a solution of benzhydryl 7-amino-3-vinyl-3-cephem-4-carboxylate hydrochloride (2.15 g) and trimethylsilylacetamide (3.93 g) in ethyl acetate (30 ml) at -20° C., and the mixture was stirred at -20° to 0° C. for 1.5 hours. To the reaction mixture was added ethyl acetate (100 ml) and water (100 ml), and the separated ethyl acetate solution was washed with a saturated aqueous sodium bicarbonate and an aqueous sodium chloride, followed by drying over anhydrous magnesium sulfate. Removal of the solvent gave a residue, which was washed with diethyl ether to obtain benzhydryl 7-(4-bromo-2-methoxyiminoacetoacetamido)-3-vinyl-3-cephem-4 -carboxylate (syn isomer) (2.5 g).

WORKUP

后处理

  1. temperaturecooling
  2. customto prepare the activated acid solution
  3. stirringthe mixture was stirred at -20° to 0° C. for 1.5 hours
  4. washthe separated ethyl acetate solution was washed with a saturated aqueous sodium bicarbonate
  5. dry with materialby drying over anhydrous magnesium sulfate
  6. customRemoval of the solvent
  7. customgave a residue, which
  8. washwas washed with diethyl ether