Реакция #366147

ord-1375ce456f464164a2eb7c73ed686286

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe reaction was reacted at 120° C. for 5 hours
  2. 2
    Температураcooled
  3. 3
    Концентрированиеconcentrated under vacuum
  4. 4
    ДругоеThe resulting residue was purified by column chromatography on silica gel

Методика

To a solution of 2-benzyloxy-5-bromo-6-nitro-benzo[de]isoquinoline-1,3-dione (0.50 g, 1.2 mmol, from Example S1-A) in DMF (5 mL) was added 3-methylpiperidine (0.47 g, 4.7 mmol). The reaction was reacted at 120° C. for 5 hours, cooled, and concentrated under vacuum. The resulting residue was purified by column chromatography on silica gel using hexane/ethyl acetate (5:1) to give 0.50 g of the title compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06362181B1uspto-grants-2002_03