HRID1065919

反应详情

EQUATION

反应方程式

HRID 1065919 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

5

PROCEDURE

实验过程

2-(2-Propynyl)oxyimino-2-(2-amino-1,3-thiazol-4-yl)acetic acid (syn isomer) (1.2 g) was suspended in tetrahydrofuran (15 ml). Phosphorus oxychloride (1.0 g) was added thereto at 0° to 5° C. and the mixture was stirred for 20 minutes at the same temperature. Trimethylsilylacetamide (0.5 g) was added thereto, the mixture was stirred for 20 minutes at the same temperature, phosphorus oxychloride (1.0 g) was added thereto, the resulting mixture was stirred for 20 minutes at 0° to 5° C., dimethylformamide (0.5 g) was added thereto and the resulting mixture was stirred for 1 hour at the same temperature. The resulting solution was added dropwise at -5° to 5° C. and pH 6.5 to 8.5 to a solution, which was prepared by adding acetone (10 ml) and tetrahydrofuran (10 ml) to a solution of 7-amino-3-carbamoyloxymethyl-3-cephem-4-carboxylic acid (1.9 g) in a mixture of sodium bicarbonate (0.4 g) and water (15 ml). The resulting mixture was stirred for 2 hours under ice-cooling keeping the pH of the mixture at 7.0 to 8.0 and then adjusted to pH 7.5. An insoluble material was filtered off and the filtrate was washed with ethyl acetate. The aqueous layer was adjusted to pH 6.0 and organic solvent in the aqueous layer was distilled off under reduced pressure. The remaining aqueous layer was adjusted to pH 4.0 and an insoluble material was filtered off. The filtrate was adjusted to pH 3.0 and precipitates were collected by filtration and dried to give 7-[2-(2-propynyl)oxyimino-2-(2-amino-1,3-thiazol-4-yl)acetamido]-3-carbamoyloxymethyl-3-cephem-4-carboxylic acid (syn isomer) (2.2 g).

WORKUP

后处理

  1. additionwas added
  2. stirringthe resulting mixture was stirred for 20 minutes at 0° to 5° C.
  3. stirringthe resulting mixture was stirred for 1 hour at the same temperature
  4. additionThe resulting solution was added dropwise at -5° to 5° C.
  5. custompH 6.5 to 8.5 to a solution, which was prepared
  6. stirringThe resulting mixture was stirred for 2 hours under ice-
  7. temperaturecooling
  8. filtrationAn insoluble material was filtered off
  9. washthe filtrate was washed with ethyl acetate
  10. distillationwas distilled off under reduced pressure
  11. filtrationan insoluble material was filtered off
  12. customprecipitates
  13. filtrationwere collected by filtration
  14. customdried