HRID249600

反应详情

EQUATION

反应方程式

HRID 249600 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 4-benzoylthiomethylthio-1,2,3-triazole (150 mg: 0.60 mMol.) in dimethylformamide (3 ml) at -60° C. is added a solution of sodium methoxide in methanol (1.26N: 0.95 ml), and the mixture is stirred for 80 minutes at -50° to -60° C. to the mixture at -7020 C. is added a solution of 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol-4-yl)-2trityloxyiminoacetamido]-3-methanesulfonyloxy-3-cephem-4carboxylic acid diphenylmethyl ester (485 mg : 0.5 mMol.) in dimethylformamide (2 ml) and the mixture is stirred at -70° C. for 20 minutes. The reaction mixture is mixed with acetic acid (0.1 ml), diluted with water, and extracted with ethyl acetate. The extract is washed with brine, dried over sodium sulfate, and concentrated. The residue is crystallized from toluene to give 7β-[(Z)-2-(2-t-butoxycarbonylaminothiazol -4-yl)- 2-trityloxyiminoacetamido]-3-(1,2,3-triazol- 4-ylthiomethylthio)-3- cephem-4-carboxylic acid diphenylmethyl ester (227 mg) as colorless crystals. Yield : 44%.

WORKUP

后处理

  1. stirringthe mixture is stirred at -70° C. for 20 minutes
  2. extractionextracted with ethyl acetate
  3. washThe extract is washed with brine
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customThe residue is crystallized from toluene