Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527264Generated: October 30, 2026

4-Hydroxybenzaldehyde → HCID 178439213, compound

https://huagongshe.com/reaction/527264

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPiperidineHCID 8082—
Reactant5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamideHCID 86701872—
SolventEthanolHCID 702—
ProductHCID 178439213HCID 17843921397%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346792B2
Source datasetuspto-grants-2016_05
ORD IDord-ed4abf0d2d844260a0c27450117ae9f3
Source noteuspto-grants-2016_05