Реакция #1435704

ord-e6b817c6b8db4602be6b0061ab2dfcd2

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(c3ccccc3)CC2c2ccc3ccc4cccc5ccc2c3c45)cc1
4-(3-phenyl-5-pyren-1-yl-4,5-dihydro-pyrazol-1-yl)-benzaldehyde
N#CC(C#N)=C1C=C(C=Cc2ccc(N3N=C(c4ccccc4)CC3c3ccc4ccc5cccc6ccc3c4c56)cc2)OC(c2ccccc2)=C1
2-(2-phenyl-6-{2-[4-(3-phenyl-5-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 6, 0.5 g (2.13 mmol) of 2-(2-methyl-6-phenyl-pyran-4-ylidene)-malononitrile and 0.961 g (2.13 mmol) of 4-(3-phenyl-5-pyren-1-yl-4,5-dihydro-pyrazol-1-yl)-benzaldehyde were added into 50 ml of ethanol, and 0.27 g (3.2 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