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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405123Generated: November 2, 2026

Piperidine → HCID 178491037, compound

https://huagongshe.com/reaction/1405123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant4-MethoxybenzaldehydeHCID 31244—
Reactant5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamideHCID 86698959—
SolventEthanolHCID 702—
ProductHCID 178491037HCID 17849103750%

Reaction Steps

5-amino-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide (1.0 g) was suspended in 10 mL of ethanol and 4-methoxybenzaldehyde (559 mg, 1.0 eq.) and piperidine (0.10 eq, 47 μL) was added. Stirred the reaction at reflux until starting material was absent and confirmed by HPLC. After reaction was complete (18 hrs) it was brought to room temperature and filtered to obtain 5-((4-methoxybenzylidene)amino)-3-(pyridin-3-ylamino)-1H-pyrazole-4-carboxamide as a yellow to orange powder. The product was washed with ethanol to remove any excess 4-methoxybenzaldehyde. Product was allowed to dry under vacuum for 1 hr (800 mg, 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916555B2
Source datasetuspto-grants-2014_12
ORD IDord-23ed94402e60496093879253c081e590
Source noteuspto-grants-2014_12