HRID1393740

反应详情

EQUATION

反应方程式

HRID 1393740 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared as follows: 2-Bromo-2′-nitroacetophenone (1.75 g, 7.2 mmol) was mixed with 50 mL of absolute EtOH along with thiourea (1.09 g, 14.4 mmol) and stirred under reflux for 2 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was basified with 20 mL of 1 N aqueous NaOH and extracted with CH2Cl2. The combined organic layers were dried (Na2SO4) and concentrated to afford essentially quantitative yield of 4-(2-nitro-phenyl)-thiazol-2-ylamine.

WORKUP

后处理

  1. custom4-(2-Nitro-phenyl)-thiazol-2-ylamine was prepared
  2. temperatureunder reflux for 2 hours
  3. concentrationconcentrated under reduced pressure
  4. extractionextracted with CH2Cl2
  5. dry with materialThe combined organic layers were dried (Na2SO4)
  6. concentrationconcentrated