反応 #78803

ord-ea6e5be525964d0ca63bb25dbda0176d

反応方程式

CN(C)C=O
DMF
Nc1ccccc1S
o-aminothiophenol
CC(=O)OC(C)=O
Ac2O
c1ccc2[nH]ccc2c1
compound ( A )
収率 32.0%
c1ccc2[nH]ccc2c1
indole
収率 32.0%

試薬

なし

溶媒

反応条件

温度
60°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONThe reaction mixture was poured
  2. 2
    ろ過the precipitated solid was collected by filtration
  3. 3
    洗浄The crude solid was washed with MeOH
  4. 4
    その他recrystallized from benzene

実験手順

A dry DMF solution of the compound (A-2) (0.01 mole) was added o-aminothiophenol (0.013 mole) and Ac2O (0.5ml) at room temperature. The mixture was stirred at 60° C. for 3 h. The reaction mixture was poured into stirred benzene and the precipitated solid was collected by filtration. The crude solid was washed with MeOH and recrystallized from benzene to afford target compound (A) (32% yield). 1H-NMR spectrum is shown in FIG. 3. Photoluminescence spectrum is shown in FIG. 4.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06713194B2uspto-grants-2004_03