HRID1111716

反应详情

EQUATION

反应方程式

HRID 1111716 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 21.1 g. (0.05 mol.) of 7-amino-3-[1-(2-sulfamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid in 500 ml. of dry methylene chloride is added in one portion a solution of 30.0 g. (0.15 mol.) of O-t-butyldiisopropylpseudourea in 50 ml. of methylene chloride. The mixture is stirred at ambient temperature for 24 hours. The precipitate is removed by filtration and the filtrate evaporated to a residue which is taken up in 200 ml. of benzene and filtered again. The filtrate is extracted with three 100 ml. portions of cold 1N hydrochloric acid. The acidic aqueous extracts are layered with ethyl acetate and the pH adjusted to 7.5 with solid sodium bicarbonate. The organic layer is separated and the aqueous phase is extracted with two 150 ml. portions of ethyl acetate. The combined extracts are dried (MgSO4), filtered and evaporated to give 7-amino-3-[1-(2-sulfamoylethyl)tetrazol-5-ylthiomethyl]-3-cephem-4-carboxylic acid t-butyl ester.

WORKUP

后处理

  1. additionTo a suspension of 21.1 g
  2. customThe precipitate is removed by filtration
  3. customthe filtrate evaporated to a residue which
  4. filtrationof benzene and filtered again
  5. extractionThe filtrate is extracted with three 100 ml
  6. customThe organic layer is separated
  7. extractionthe aqueous phase is extracted with two 150 ml
  8. dry with materialThe combined extracts are dried (MgSO4)
  9. filtrationfiltered
  10. customevaporated