HRID895068

反应详情

EQUATION

反应方程式

HRID 895068 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

7-Amino-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid (1.0 g., 2.68 mmol.) was suspended in 10 ml. of dry dimethylformamide and 1.12 ml. of triethylamine was added followed by 85 drops of formamide. A solution of 0.91 g. (2.68 mmol.) of the activated ester of α-t-butoxycarbonylthienylacetamide, prepared as described above, in 2 ml. of dimethylformamide was added and the reaction mixture was stirred at 25° for three hours. An additional 0.45 g. of activated ester was then added and the mixture stirred another five hours. Ether (ca. 300 ml.) was added and the solution was decanted. The remaining oily material was washed with ether, dissolved in water and the aqueous solution was extracted with ethyl acetate. The pH of the ethyl acetate solution was adjusted to 1.5 by addition of dilute hydrochloric acid. Extraction with ethyl acetate and evaporation of the solvent gave 7-(α-t-butoxycarbonylthienylacetamido)-3-(1-carboxymethyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid.

WORKUP

后处理

  1. stirringthe mixture stirred another five hours
  2. customthe solution was decanted
  3. washThe remaining oily material was washed with ether
  4. dissolutiondissolved in water
  5. extractionthe aqueous solution was extracted with ethyl acetate
  6. additionThe pH of the ethyl acetate solution was adjusted to 1.5 by addition of dilute hydrochloric acid
  7. extractionExtraction
  8. customwith ethyl acetate and evaporation of the solvent