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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405133Generated: November 1, 2026

4-Hydroxybenzaldehyde → HCID 178441007, compound

https://huagongshe.com/reaction/1405133

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantHCID 86701893HCID 86701893—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178441007HCID 178441007—

Reaction Steps

5-amino-3-((4-(tert-butyl)phenyl)amino)-1H-pyrazole-4-carboxamide was then suspended in 8 mL EtOH and 4-hydroxybenzaldehyde (325 mg, 1 eq.) and piperidine (4 drops) were added. Stirred at reflux until intermediate was absent (HPLC). After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain 3-((4-(tert-butyl)phenyl)amino)-5-((4-hydroxybenzylidene)amino)-1H-pyrazole-4-carboxamide as a yellow powder. Powder was washed with EtOH to remove any excess 4-hydroxybenzaldehyde. Product was allowed to dry under vacuum for 1 hr.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916555B2
Source datasetuspto-grants-2014_12
ORD IDord-417509f23fcf4b7eb29f1f3149ab2f6d
Source noteuspto-grants-2014_12