HRID569402

反应详情

EQUATION

反应方程式

HRID 569402 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a suspension of benzhydryl 7-[2-(2-aminothiazol-4-yl)-2-tert-butoxycarbonylmethoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylate (syn isomer)(15.0 g) in anisole (15 ml) was added 2,2,2-trifluoroacetic acid (60 ml) under ice-cooling with stirring, and the stirring was continued at 10° to 15° C. for 80 minutes. After the reaction mixture was poured into diisopropyl ether (600 ml), the insoluble substance was collected by filtration and then dried. This substance (11.2 g) was dissolved in an aqueous solution of sodium bicarbonate so as to adjust the resultant solution to pH 6.0, and then chromatographed on alumina (44.8 ml) using 5% aqueous sodium acetate as an eluent. The fractions containing the desired compound were collected and evaporated to dryness to give 7-[2-(2-aminothiazol-4-yl)-2-carboxymethoxyiminoacetamido]-3-vinyl-3-cephem-4-carboxylic acid (syn isomer)(3.55 g), mp>250° C.

WORKUP

后处理

  1. temperaturecooling
  2. filtrationthe insoluble substance was collected by filtration
  3. customdried
  4. dissolutionThis substance (11.2 g) was dissolved in an aqueous solution of sodium bicarbonate so as
  5. customchromatographed on alumina (44.8 ml)
  6. additionThe fractions containing the desired compound
  7. customwere collected
  8. customevaporated to dryness