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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1664481Generated: October 25, 2026

Triethylamine → 5-Amino-1-cyclohexyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1664481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-(Ethoxymethylene)propanedinitrileHCID 67152—
ReactantCyclohexylhydrazine hydrochlorideHCID 207836—
SolventEthanolHCID 702—
Product5-Amino-1-cyclohexyl-1H-pyrazole-4-carbonitrileHCID 690005—

Reaction Steps

First ethoxymethylenemalononitrile (2.43 g, 19.9 mmol) and then 8 ml of triethylamine are added to a solution of cyclohexylhydrazine hydrochloride (3 g, 19.9 mmol) in 36 ml of ethanol at room temperature. The mixture is refluxed for 20 min and then cooled. The solvent is stripped off in a rotary evaporator, and the residue is taken up in DCM, washed with aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product is chromatographed on silica gel (mobile phase: dichloromethane/methanol 0-10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039477B2
Source datasetuspto-grants-2011_10
ORD IDord-677fc99bffc945709f49fc9b470fb088
Source noteuspto-grants-2011_10