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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049212Generated: November 1, 2026

4-Nitrobenzaldehyde → HCID 178513716, compound

https://huagongshe.com/reaction/1049212

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 numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-1955b9cd919846a5ace1245eb986308c
Source noteuspto-grants-2016_07