Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527281Generated: October 30, 2026

Piperidine → HCID 178491037, compound

https://huagongshe.com/reaction/527281

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 numberUS09346792B2
Source datasetuspto-grants-2016_05
ORD IDord-f246ff9e9f9e4c8e84503f0a8cdc2e3e
Source noteuspto-grants-2016_05