HRID2419145

反应详情

EQUATION

反应方程式

HRID 2419145 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

A slurry of 3-[(1,3-benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinone (see example 37), m-trifluoromethylbenzaldehyde (10 ml, excess) and acetic acid/piperidine (1 ml) in 250 ml of anhydrous glyme is heated at reflux for 7 days. The reaction mixture is concentrated in vacuo and the oily residue extracted with hexane. The solid thus obtained is slurried in 1000 ml of dichloromethane and stirred at room temperature overnight. The slurry is filtered and the filtrate concentrated in vacuo. The solid residue thus obtained is recrystallized from dimethylformamide to yield 500 mg of the title compound, melting point 268°-269° C.

WORKUP

后处理

  1. temperatureat reflux for 7 days
  2. concentrationThe reaction mixture is concentrated in vacuo
  3. extractionthe oily residue extracted with hexane
  4. customThe solid thus obtained
  5. filtrationThe slurry is filtered
  6. concentrationthe filtrate concentrated in vacuo
  7. customThe solid residue thus obtained
  8. customis recrystallized from dimethylformamide