Реакция #172452

ord-931fa5ca027e4432bddb66ea710f5aac

Растворители

Условия реакции

Температура
60°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe solvent was evaporated off
  2. 2
    Промывкаthe residue was washed with ethanol
  3. 3
    ДругоеThe residue was purified by silica gel column chromatography
  4. 4
    Промывкаwashed with ethanol

Методика

In 5 ml of ethanol and 1.5 ml of tetrahydrofuran were dissolved 120 mg (0.35 mmol) of 5-[2-(8-methoxy-2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizine-9-yl)vinyl]thiophene-2-carboaldehyde and 123 mg (0.39 mmol) of 2-(3-cyano-4-methyl-5-phenyl-5-trifluoromethyl-2(5H)-furanylidene)propanedinitrile. The mixture was stirred with heating at 60° C. for 3 hours. The solvent was evaporated off and the residue was washed with ethanol. The residue was purified by silica gel column chromatography and washed with ethanol to give 100 mg of a dark brown crystal (yield: 44.4%; mp: 156-160° C.)

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08846955B2uspto-grants-2014_09