Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 789785 | HCID 789785 | — |
| Reactant | HCID 18458006 | HCID 18458006 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73446799 | HCID 73446799 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07211335B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-e6b817c6b8db4602be6b0061ab2dfcd2 |
|---|
| Source note | uspto-grants-2007_05 |
|---|