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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381108Generated: November 4, 2026

Piperazine → 2-(Piperazin-1-yl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/1381108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-ChloronicotinonitrileHCID 81079—
SolventEthanolHCID 702—
Product2-(Piperazin-1-yl)pyridine-3-carbonitrileHCID 273720372.5%

Reaction Steps

A mixture of piperazine (0.5 mol) and 2-chloro-3-cyanopyridine (0.1 mol) in absolute ethanol (225 ml) was heated at reflux for 16 hours. The cooled mixture was filtered to remove precipitated piperazine hydrochloride and the filtrate evaporated in vacuo. The residue was diluted with water (200 ml), made basic (pH>10) with 5N sodium hydroxide and extracted with ether (5×300 ml). The combined extracts were dried (MgSO4) and evaporated in vacuo affording 13.6 g of a white solid (72.5% yield); mp 99°-103° C. Spectral data are consistent with the assigned structure. This material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04585773
Source datasetuspto-grants-1986_04
ORD IDord-d62e1a7ac55549b5b5f2d3d825b1ec91
Source noteuspto-grants-1986_04