Reacción #1253195

ord-5e0360dfac71424c9cd91d092aa031af

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathe mixture heated
  2. 2
    Temperaturato reflux for 18 hours
  3. 3
    OtroThe solvent is removed
  4. 4
    Otrothe residue chromatographed (silica
  5. 5
    Lavadoeluting with a gradient
  6. 6
    Temperaturaincreasing in polarity from 0 to 4% methanol in dichloromethane)

Procedimiento

1-(2-Fluoroethyl)-2-oxopiperazine trifluoroacetate (6.1 g) is dissolved in acetonitrile (100 ml). N,N-Diisopropylethylamine (13 ml) is added to the mixture, followed by 3,4-difluoronitrobenzene (3.39 g) and the mixture heated to reflux for 18 hours. The solvent is removed and the residue chromatographed (silica; eluting with a gradient increasing in polarity from 0 to 4% methanol in dichloromethane) to give 3-fluoro-4-(4-{2-fluoroethyl}-3-oxopiperazin-1-yl)nitrobenzene.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06613349B2uspto-grants-2003_09