Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 789785 | HCID 789785 | — |
| Reactant | HCID 18458005 | HCID 18458005 | — |
| Product | HCID 73446796 | HCID 73446796 | — |
Reaction Steps
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.
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-118e6946cdca41aabad9ebf40142de05 |
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| Source note | uspto-grants-2007_05 |
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