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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527293Generated: October 29, 2026

4-Hydroxybenzaldehyde → HCID 178513725, compound

https://huagongshe.com/reaction/527293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantHCID 86701896HCID 86701896—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178513725HCID 178513725—

Reaction Steps

4-((5-amino-4-carbamoyl-1H-pyrazol-3-yl)amino)benzoic acid 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 4-((4-carbamoyl-5-((4-hydroxybenzylidene)amino)-1H-pyrazol-3-yl)amino)benzoic acid 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 numberUS09346792B2
Source datasetuspto-grants-2016_05
ORD IDord-b689c35d7aff409f931ec3757364af92
Source noteuspto-grants-2016_05