反応 #722508

ord-acaf6a60582d42df8570536b066bf716

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooling
  2. 2
    workup.STIRRINGThe reaction mixture was stirred for 2 hours at room temperature
  3. 3
    その他the chloroform layer was separated
  4. 4
    乾燥After drying over magnesium sulfate
  5. 5
    その他the solvent was evaporated under reduced pressure

実験手順

3-(3-(4-(4-Chlorophenyl)piperazin-1-yl)propyl)-4,5,6,7-tetrahydroindole (0.5 g) obtained in Example 161 and triethylamine (0.6 ml) were dissolved in dichloromethane (10 ml) and acetyl chloride (0.3 g) was added under ice-cooling with stirring. The reaction mixture was stirred for 2 hours at room temperature and an aqueous potassium carbonate solution is added, and the chloroform layer was separated. After drying over magnesium sulfate, the solvent was evaporated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography to give 1-acetyl-3-(3-(4-(4chlorophenyl)piperazin-1-yl)propyl)-4,5,6,7-tetrahydroindole.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06187774B1uspto-grants-2001_02