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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049183Generated: October 31, 2026

Piperidine → HCID 178491037, compound

https://huagongshe.com/reaction/1049183

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 numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-ed9c90ba29104031903ec602f73f123b
Source noteuspto-grants-2016_07