Реакция #1435705

ord-d2ece438a18f4c03ad8651163df4125f

Уравнение реакции

C1CCNCC1
piperidine
CC1=CC(=C(C#N)C#N)C=C(c2ccccc2)O1
2-(2-methyl-6-phenyl-pyran-4-ylidene)-malononitrile
O=Cc1ccc(N2N=C(c3ccc4ccc5cccc6ccc3c4c56)CC2c2ccccc2)cc1
4-(5-phenyl-3-pyren-1-yl-4,5-dihydro-pyrazol-1-yl)benzaldehyde
N#CC(C#N)=C1C=C(C=Cc2ccc(N3N=C(c4ccc5ccc6cccc7ccc4c5c67)CC3c3ccccc3)cc2)OC(c2ccccc2)=C1
2-(2-phenyl-6-{2-[4-(5-phenyl-3-pyren-1-yl-4,5-dihydro-pyrazol-1-yl)-phenyl]-vinyl}-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 8, 0.24 g (1.0 mmol) of 2-(2-methyl-6-phenyl-pyran-4-ylidene)-malononitrile and 0.46 g (1.0 mmol) of 4-(5-phenyl-3-pyren-1-yl-4,5-dihydro-pyrazol-1-yl)benzaldehyde were added into 20 ml of ethanol, and 0.13 g (1.53 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