HRID1274205

反应详情

EQUATION

反应方程式

HRID 1274205 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

In a 100 ml flask is placed triphenylphosphine (80 mg, 10%), PdCl2 (40 mg, 5%) and 2-(4'-fluorophenyl)-4-(4'-bromophenyl)thiazole (0.98 g, 2.9 mmol) in 20 ml of diethylamine. After stirring for 15 min under N2 atmosphere, CuI (30 mg, 5%) and 1-dimethylamino-2-propyne (0.27 g, 3.18 mmol) in 20 ml of acetonitrile are added to the mixture. After 18 h of heating, the solvent is evaporated under reduced pressure and the residue is filtered through silica gel pad (50 g) using CHCl3 (400 mL) and 2% MeOH in CHCl3 (400 mL). A large portion of unreacted 2-(4'-fluorophenyl)-4-(4'-bromophenyl)thiazole is recovered after removal of chloroform filtrate (0.55 g, 56%). The second part of the filtrate (2% MeCH in CHCl3) is concentrated and the residual solid is then purified over silca gel column eluting with 2% MeOH in CHCl3. 2-(4'-fluorophenyl)-4-[4'-(3-dimethylamino-2-propyn-1-yl)phenyl]thiazole is obtained after concentration and trituration with hexane (0.25 g, 27% yield), mp. 98-9° C.

WORKUP

后处理

  1. customIn a 100 ml flask is placed
  2. temperatureAfter 18 h of heating
  3. customthe solvent is evaporated under reduced pressure
  4. filtrationthe residue is filtered through silica gel pad (50 g)
  5. customA large portion of unreacted 2-(4'-fluorophenyl)-4-(4'-bromophenyl)thiazole is recovered
  6. customafter removal of chloroform filtrate (0.55 g, 56%)
  7. concentrationThe second part of the filtrate (2% MeCH in CHCl3) is concentrated
  8. customthe residual solid is then purified over silca gel column
  9. washeluting with 2% MeOH in CHCl3