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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405151Generated: October 30, 2026

4-Nitrobenzaldehyde → HCID 178513716, compound

https://huagongshe.com/reaction/1405151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrobenzaldehydeHCID 541—
Reactant5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamideHCID 86698956—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178513716HCID 178513716—

Reaction Steps

5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide (100 mg) was suspended in EtOH (4 mL) and 4-nitrobenzaldehyde (1 eq.) and piperidine (1 drop) 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-((3-chlorophenyl)amino)-5-((4-nitrobenzylidene)amino)-1H-pyrazole-4-carboxamide as a yellow powder. Powder was washed with EtOH. 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-114068e45d974091a70ddcd544e95ec5
Source noteuspto-grants-2014_12