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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714798Generated: October 31, 2026

Piperazine → 7-(Piperazin-1-yl)furo[2,3-c]pyridine

https://huagongshe.com/reaction/1714798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Chlorofuro[2,3-c]pyridineHCID 12826107—
SolventEthylene GlycolHCID 174—
Product7-(Piperazin-1-yl)furo[2,3-c]pyridineHCID 1839972675%

Reaction Conditions

Temperature140 °C

Reaction Steps

In 100 ml of ethylene glycol 8.6 g of anhydrous piperazine was dissolved, and to which 7-chlorofuro[2,3-c]pyridine was added, followed by an overnight's stirring at 140° C. After cooling, saturated aqueous sodium hydrogencarbonate solution was added to the solution, which was then extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified on silica gel column chromatography to provide 1.52 g (75%) of 7-piperazin-1-ylfuro[2,3-c]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-205f417251854367a6bd6884850545e7
Source noteuspto-grants-2010_09