HRID1988671

反应详情

EQUATION

反应方程式

HRID 1988671 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
180 °C

PROCEDURE

实验过程

A mixture of 5-(4-bromophenyl)-1-methyl-2-pyrrolidinone (141 mg, 0.56 mmol), 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (111 mg, 0.58 mmol), copper (I) iodide (10 mol %, 11 mg, 0.06 mmol), N,N-dimethylglycine (20 mol %, 12 mg, 0.12 mmol) and potassium carbonate (162 mg, 1.17 mmol) in dimethylsulfoxide (3 ml) was stirred at 180° C. in a microwave reactor for a total of 2 h. The reaction mix was filtered through a 5 g pre-packed silica column washing through with dichloromethane (20 ml), the filtrate was washed with water (50 ml) and the organic layer dried over sodium sulphate. The solvent was removed by rotary evaporation and the sample purified by mass directed auto prep. The final product was partitioned between dichloromethane (3 ml) and water (3 ml). The organic layer was separated and solvent removed by rotary evaporation to give the title compound as a brown oil (14 mg, 7%)

WORKUP

后处理

  1. additionThe reaction mix
  2. filtrationwas filtered through a 5 g pre-packed silica column
  3. washwashing through with dichloromethane (20 ml)
  4. washthe filtrate was washed with water (50 ml)
  5. dry with materialthe organic layer dried over sodium sulphate
  6. customThe solvent was removed by rotary evaporation
  7. customthe sample purified by mass
  8. customThe final product was partitioned between dichloromethane (3 ml) and water (3 ml)
  9. customThe organic layer was separated
  10. customsolvent removed by rotary evaporation