Reacción #43311

ord-03e023041a31460a9e95a92d281c2f32

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónConcentrating
  2. 2
    Otrothe reaction liquid under reduced pressure
  3. 3
    Otrothe resulting residue was purified on silica gel column chromatography (C-300, methanol: chloroform=1:20-1:10)

Procedimiento

4-Benzyloxy-1-(4-hydroxyphenyl)-1H-pyridin-2-one (150 mg, 0.511 mmol), 2-(dimethylamino)ethanol (0.057 mL, 0.562 mmol), triphenylphosphine (269 mg, 1.02 mmols) and diethyl azodicarboxylate (0.163 mL, 1.02 mmols) were stirred overnight in THF (4 mL). Concentrating the reaction liquid under reduced pressure, the resulting residue was purified on silica gel column chromatography (C-300, methanol: chloroform=1:20-1:10) to provide the title compound (124 mg, 60%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07732456B2uspto-grants-2010_06