Reaktion #1584567

ord-2362a828c7214f72a7b63c730646b109

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Waschenwashed with water and saturated brine
  2. 2
    Trocknendried over anhydrous magnesium sulfate
  3. 3
    Einengenconcentrated under reduced pressure
  4. 4
    SonstigeThe obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol)

Vorschrift

To a suspension of 1-(2,3-dimethyl-2H-indazol-5-yl)-4-hydroxypyridin-2(1H)-one (50 mg), (5-bromothiophen-2-yl)methanol (76 mg) and triphenylphosphine (154 mg) in tetrahydrofuran (5 ml) was added bis(2-methoxyethyl) azodicarboxylate (138 mg) at room temperature, and the mixture was stirred at the same temperature for 3 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give the title compound (13 mg).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09199963B2uspto-grants-2015_12