تفاعل #214828

ord-aa5c6506ad1647c7b22aec2dd585c4fd

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed successively with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution
  2. 2
    تجفيفthe organic phase is dried over sodium sulphate
  3. 3
    أخرىevaporated in vacuo
  4. 4
    أخرىThe residue is chromatographed on silica gel thick layer plates with toluene/ethyl acetate, 1:1

الإجراء التجريبي

A solution of 410 mg (2.03 mmols) of m-chloroperbenzoic acid in 10 ml of methylene chloride is added to a solution of 1.10 g (1.85 mmols) of a mixture of isomers consisting of 7β-phenylacetylamino-3-phenylthio-3-cephem-4-carboxylic acid diphenylmethyl ester and 7β-phenylacetylamino-3-phenylthio-2-cephem-4α-carboxylic acid diphenylmethyl ester in 11 ml of methylene chloride at 0° C. and the mixture is stirred in an ice bath for 30 minutes. The reaction mixture is diluted with ethyl acetate and washed successively with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution and the organic phase is dried over sodium sulphate and evaporated in vacuo. The residue is chromatographed on silica gel thick layer plates with toluene/ethyl acetate, 1:1. 7β-Phenylacetylamino-3-phenylthio-3-cephem-4-carboxylic acid diphenylmethyl ester 1-oxide of Rf value ~0.38 (silica gel; toluene/ethyl acetate, 1:1) is obtained and after recrystallisation from methylene chloride/diethyl ether melts at 180° C. with decomposition.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04256739uspto-grants-1981_03