Реакция #1435703

ord-118e6946cdca41aabad9ebf40142de05

Уравнение реакции

C1CCNCC1
piperidine
CC1=CC(=C(C#N)C#N)C=C(c2ccccc2)O1
2-(2-methyl-6-phenyl-pyran-4-ylidene)-malononitrile
COc1ccccc1C1=NN(c2ccc(C=O)cc2)C(c2ccccc2)C1
4-[3-(2-methoxy-phenyl)-5-phenyl-4,5-dihydro-pyrazol-1-yl]-benzaldehyde
COc1ccccc1C1=NN(c2ccc(C=CC3=CC(=C(C#N)C#N)C=C(c4ccccc4)O3)cc2)C(c2ccccc2)C1
2-[2-(2-{4-[3-(2-methoxy-phenyl)-5-phenyl-4,5-dihydro-pyrazol-1-yl]-phenyl}-vinyl)-6-phenyl-pyran-4-ylidene]-malononitrile

Растворители

Условия реакции

Температура
75°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added

Методика

As shown in the following reaction 5, 0.197 g (0.84 mmol) of 2-(2-methyl-6-phenyl-pyran-4-ylidene)-malononitrile and 0.30 g (0.84 mmol) of 4-[3-(2-methoxy-phenyl)-5-phenyl-4,5-dihydro-pyrazol-1-yl]-benzaldehyde were added into 20 ml of alcohol (ethanol), and 0.10 g (1.2 mmol) of piperidine was added thereto. The reaction solution was heated at 75° C. for 10 hours.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07211335B2uspto-grants-2007_05