Reacción #78803

ord-ea6e5be525964d0ca63bb25dbda0176d

Ecuación de reacción

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

Reactivos

Ninguno

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe reaction mixture was poured
  2. 2
    Filtraciónthe precipitated solid was collected by filtration
  3. 3
    LavadoThe crude solid was washed with MeOH
  4. 4
    Otrorecrystallized from benzene

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06713194B2uspto-grants-2004_03