Reacción #2439944

ord-a0bc3c1d87694bddbeec0b411166dc4c

Ecuación de reacción

CC(=O)Cl
acetyl chloride
Nc1cccc(C(=O)c2ccc3c(c2)CC(=O)N3)c1
5-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one
CC(=O)Nc1cccc(C(=O)c2ccc3c(c2)CC(=O)N3)c1
N-[3-(2-Oxo-2,3-dihydro-1H-indole-5-carbonyl)-phenyl]-acetamide
Rendimiento 61.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturato reflux for 3 h
  2. 2
    FiltraciónThe tan precipitate was filtered

Procedimiento

A dry 25 mL flask was charged with acetyl chloride (0.273 g, 3.48 mmol) and THF (5 mL). 5-(3-Amino-benzoyl)-1,3-dihydro-indol-2-one (as prepared in Example 1, 0.675 g, 2.67 mmol) was added to the THF solution of the acid chloride, and the mixture was allowed to reflux for 3 h. The reaction mixture was then allowed to cool to room temperature. The tan precipitate was filtered to afford N-[3-(2-Oxo-2,3-dihydro-1H-indole-5-carbonyl)-phenyl]-acetamide (0.478 g, 1.48 mmol, 61%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07749530B2uspto-grants-2010_07