Реакция #43311

ord-03e023041a31460a9e95a92d281c2f32

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07732456B2uspto-grants-2010_06