Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 789785 | HCID 789785 | — |
| Reactant | 4-(3,5-diphenyl-4,5-dihydro-1H-pyrazol-1-yl)benzaldehyde | HCID 2792090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 73446798 | HCID 73446798 | — |
Reaction Steps
As shown in the following reaction 4, 0.4 g (1.7 mmol) of 2-(2-methyl-6phenyl-pyran-4-ylidene)-malononitrile and 0.55 g (1.7 mmol) of 4-(3,5-diphenyl-4,5-dihydro-pyrazol-1-yl)-benzaldehyde} were added into 40 ml of ethanol, and 0.17 g (2.0 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-138ba86011e749858effdec0af4739ac |
|---|
| Source note | uspto-grants-2007_05 |
|---|
