HRID1395489

反应详情

EQUATION

反应方程式

HRID 1395489 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

5-Methyl-1,3,4-thiadiazole-2-thiol (0.16 g) was dissolved in a mixture of pH 6.5 phosphate buffer (5 ml) and acetone (10 ml). To this solution was added 2,2,2-trichloroethyl 2-bromomethyl-2-methyl-6-(2-phenylacetamido)penam-3-carboxylate (0.54 g) and the mixture was stirred for 3 hours at room temperature. The reaction mixture was concentrated under reduced pressure and acetone was distilled off and thereafter the residue was extracted with ethyl acetate. The ethyl acetate layer was washed with sodium bicarbonate aqueous solution and then with water and thereafter dried over magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography on silica gel using chloroform as developing solvent to give oily 2,2,2-trichloroethyl 2-(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl-2-methyl-6-(2-phenylacetamido)-penam-3-carboxylate (0.09 g) from the second and third fractions each of which was separated into about 30 ml.

WORKUP

后处理

  1. concentrationThe reaction mixture was concentrated under reduced pressure and acetone
  2. distillationwas distilled off
  3. extractionthe residue was extracted with ethyl acetate
  4. washThe ethyl acetate layer was washed with sodium bicarbonate aqueous solution
  5. dry with materialwith water and thereafter dried over magnesium sulfate
  6. distillationThe solvent was distilled off
  7. customthe residue was purified by column chromatography on silica gel