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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1736538Generated: November 3, 2026

Cyclopentylhydrazine hydrochloride → 1-cyclopentyl-3-ethyl-4-cyano-5-amino-1H-pyrazole

https://huagongshe.com/reaction/1736538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylhydrazine hydrochlorideHCID 212349—
Reactant2-(1-Ethoxypropylidene)malononitrileHCID 231470—
ReactantSodium MethoxideHCID 10942334—
SolventEthanolHCID 702—
Product1-cyclopentyl-3-ethyl-4-cyano-5-amino-1H-pyrazoleHCID 1587126970%

Reaction Steps

Cyclopentylhydrazine hydrochloride (20.9 g, 0.1 moles), 97% sodium methoxide (5.6 g, 0.1 moles) and ethanol (100 ml) were combined and stirred at room temperature under argon for 2.5 hours. (1-Ethoxypropylidene)malononitrile was added to the reaction mixture and the mixture was refluxed for 21 hours. The reaction mixture was cooled and the solvent was removed in vacuo. The residue was treated with water (150 ml) and the obtained precipitate was collected by filtration, washed with water and dried in a vacuum oven for 24 hours to afford 14.2 g (70%) of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carbonitrile as a brown powder, m.p. 171°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05541187
Source datasetuspto-grants-1996_07
ORD IDord-7d96401eb3e247d9ba211e684e72eeec
Source noteuspto-grants-1996_07