HRID1906529

反应详情

EQUATION

反应方程式

HRID 1906529 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

1.9 g of 2-(4-tert-butylphenyl)-7-chloro-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one was suspended in a mixture of 20 ml of ethanol and 10 ml of dimethylformamide, and 5 ml of concentrated aqueous ammonia was added dropwise to the suspension while maintaining at a temperature of 60° C. to 70° C. After heating at that temperature for 2 hours, the mixture was cooled and the precipitate formed was separated by filtration to obtain 1.3 g of 7-amino-2-(4-tert-butylphenyl)-6-nitro-5H-[1,3,4]thiadiazolo[3,2-a]pyrimidin-5-one as pale yellow prisms having a melting point higher than 300° C.

WORKUP

后处理

  1. additionwas added dropwise to the suspension
  2. temperaturewhile maintaining at a temperature of 60° C. to 70° C
  3. temperatureAfter heating at that temperature for 2 hours
  4. temperaturethe mixture was cooled
  5. customthe precipitate formed
  6. customwas separated by filtration