Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405139Generated: November 3, 2026

4-Fluoro-3-methoxybenzaldehyde → HCID 178492215, compound

https://huagongshe.com/reaction/1405139

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluoro-3-methoxybenzaldehydeHCID 2737358—
Reactant5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamideHCID 86698959—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 178492215HCID 178492215—

Reaction Steps

5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide (100 mg) was suspended in EtOH (3 mL) and 4-Fluoro-3-methoxybenzaldehyde (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 5-((4-fluoro-3-methoxybenzylidene)amino)-3-(pyridin-3-ylamino)-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-b7090b31894440d3a5a9c62569375eaa
Source noteuspto-grants-2014_12