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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714780Generated: October 30, 2026

Piperazine → Quipazine

https://huagongshe.com/reaction/1714780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant2-ChloroquinolineHCID 11928—
ReactantSodium BicarbonateHCID 516892—
SolventEthylene GlycolHCID 174—
ProductQuipazineHCID 5011102.2%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution formed by dissolving 4.31 g of anhydrous piperazine in 30 ml of ethylene glycol, 818 mg of 2-chloroquinoline was added, and stirred at 140° C. for 2 hours. After cooling the reaction mixture, saturated aqueous sodium hydrogencarbonate solution was added, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified on silica gel column chromatography (chloroform:methanol=2:1) to provide 1.09 g (100%) of 2-piperazin-1-ylquinoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-4fa9ca7447264c219f8376d75b571aba
Source noteuspto-grants-2010_09