Реакция #1159046

ord-c97b8e8f99534d54b79559d3d741c3b7

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеIt was concentrated
  2. 2
    Другоеthe residue was purified by column chromatography (silica gel, EtOAc/Hexane=1:5)

Методика

A solution of 2-imino-3-benzoyl-7-dimethylamino 4-(3-methoxy-4,5-methylenedioxyphenyl)-chromane (26 mg, 0.059 mmol) and triethylamine (0.1 ml) in ethanol (5 ml) was refluxed for 12 h. It was concentrated, and the residue was purified by column chromatography (silica gel, EtOAc/Hexane=1:5) to give 18 mg (72%) of the title compound. 1H NMR (CDCl3): 7.40-7.30 (m, 2H), 7.18-7.14 (m, 2H), 6.86 (d, 1H), 6.50-6.34 (m, 2H), 6.00 (d, 1H), 5.85-5.81 (m, 2H), 5.73 (d, 1H), 4.73 (s, 1H), 3.67 (s, 3H), 2.91 (s, 6H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06906203B1uspto-grants-2005_06