HRID18692

反应详情

EQUATION

反应方程式

HRID 18692 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
7.5 °C

PROCEDURE

实验过程

7-amino-3-(1-sulfomethyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (5 g) was dissolved in water (19 ml) using 30% w/w sodium hydroxide (1.5 g in 8 ml water) and sodium bicarbonate (1 g), O-formylmandeloyl chloride (2.45 g) was added at 0-5° C. and maintained at 5-10° C. over a period of 1-2 hours. After the completion of reaction, the reaction mixture was acidified with conc. HCl (2.6 g) and maintained under stirring at 28-30° C. over 2-3 hours. After the completion of reaction, sodium bicarbonate (˜3.5 g) was added to set the pH 5±1. The solution was added to a solution of N,N′-di-(p-anisyl)ethylenediamine diacetate (11.7 g) in water (40 mL) and isopropyl alcohol (40 mL) and stirred well at 25-30° C. After stirring for 2-3 hours, the reaction mixture was cooled to 5-10° C., filtered, washed with chilled water (0-5° C.) and isopropyl alcohol (0-5° C.) and dried the material under vacuum at ˜40° C. to get N,N′-di-(p-anisyl)ethylenediamine salt of 7-D-mandelamido-3-(((1-sulfomethyl-1H-tetrazol-5-yl)thio)methyl)-3-cephem-4-carboxylic acid (6.4 g). Step-(ii)

WORKUP

后处理

  1. additionwas added at 0-5° C.
  2. customAfter the completion of reaction
  3. temperaturemaintained
  4. additionwas added
  5. stirringstirred well at 25-30° C
  6. stirringAfter stirring for 2-3 hours
  7. temperaturethe reaction mixture was cooled to 5-10° C.
  8. filtrationfiltered
  9. washwashed with chilled water (0-5° C.) and isopropyl alcohol (0-5° C.)
  10. customdried the material under vacuum at ˜40° C.