Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 789785 | HCID 789785 | — |
| Reactant | HCID 18458009 | HCID 18458009 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73446800 | HCID 73446800 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07211335B2 |
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| Source dataset | uspto-grants-2007_05 |
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| ORD ID | ord-d2ece438a18f4c03ad8651163df4125f |
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| Source note | uspto-grants-2007_05 |
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