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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182136Generated: October 26, 2026

Piperazine → 2-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)Pyrazine

https://huagongshe.com/reaction/2182136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant3-(6-Chloro-pyrazin-2-yloxymethyl)-benzonitrileHCID 22481973—
SolventEthanolHCID 702—
Product2-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)PyrazineHCID 9857335—

Reaction Steps

A mixture of 3-(6-chloro-pyrazin-2-yloxymethyl)-benzonitrile I-3a (3.53 g, 14.4 mmol) and piperazine (12.4 g, 143.70 mmol) in ethanol (144 mL) was stirred under reflux for 48 h. The reaction mixture was concentrated to dryness and the residue was dissolved in ethyl acetate (300 mL). The ethyl acetate solution was washed with H2O (4×125 mL), brine (125 mL), dried (Na2SO4), filtered, and concentrated to dryness. The crude material was chromatographed over Silica Gel (40 g) using 5% methanol/methylene chloride with 1% NH4OH as the eluant to give 3.03 g of the desired product (I-3b) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894050B2
Source datasetuspto-grants-2005_05
ORD IDord-afc22ffcb6c54661ba92ff115196f07b
Source noteuspto-grants-2005_05