Реакция #1435706

ord-384fba05dab5467992f6cf3c3f64830d

Уравнение реакции

C1CCNCC1
piperidine
CC1=CC(=C(C#N)C#N)C=C(C(C)C)O1
2-(2-isopropyl-6-methyl-pyran-4-ylidene)-malononitrile
O=Cc1ccc(N2N=C(c3ccccc3)CC2c2ccccc2)cc1
4-(3,5-diphenyl-4,5-dihydro-pyrazol-1-yl)-benzaldehyde
CC(C)C1=CC(=C(C#N)C#N)C=C(C=Cc2ccc(N3N=C(c4ccccc4)CC3c3ccccc3)cc2)O1
2-(2-{2-[4-(3,5-diphenyl-4,5-dihydro-pyrazol-1-yl)-phenyl]-vinyl}-6-isopropyl-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 9, 0.5 g (2.5 mmol) of 2-(2-isopropyl-6-methyl-pyran-4-ylidene)-malononitrile and 0.815 g (2.5 mmol) of 4-(3,5-diphenyl-4,5-dihydro-pyrazol-1-yl)-benzaldehyde were added into 20 ml of ethanol, and 0.32 g (3.75 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