HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Hydroxybenzaldehyde → HCID 178439213, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamide | HCID 86701872 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178439213 | HCID 178439213 | 97% |
Reaction Steps
5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamide (850 mg) was suspended in 15 mL of ethanol and 4-hydroxybenzaldehyde (601 mg, 1.5 eq.) and piperidine (0.50 eq, 168 μL) was added. Stirred the reaction at reflux until starting material was absent and confirmed by HPLC. After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain 5-((4-hydroxybenzylidene)amino)-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamide as a yellow to orange powder. The product was washed with ethanol to remove any excess 4-hydroxybenzaldehyde. Product was allowed to dry under vacuum for 1 hr (1.15 g, 97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346792B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-ed4abf0d2d844260a0c27450117ae9f3 |
| Source note | uspto-grants-2016_05 |