Реакция #50556

ord-53b23d7d80234aec8d63a40301135afd

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеevaporated
  2. 2
    Другоеthe residue was chromatographed (silica, dichloromethane)
  3. 3
    Другоеto give
  4. 4
    Другоеafter crystallisation (hexane/ethyl acetate)

Методика

1,1'-carbonyldiimidazole (4.9 g) was added batchwise to pyruvic acid (2.6 g) in dichloromethane (100 ml), and after 0.5 hours 2,6-dimethyl-4-(1-phenyl-1H-pyrazol-3-yl) aminophenol (2.8 g) was added. The mixture was left for 16 hours, then evaporated, and the residue was chromatographed (silica, dichloromethane) to give, after crystallisation (hexane/ethyl acetate), the title product (1.0 g) mp 123°-125°.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05428044uspto-grants-1995_06