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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544235Generated: November 1, 2026

Piperazine → HCID 70495615, compound

https://huagongshe.com/reaction/544235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant6-Bromo-7-chloro-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 12733873—
SolventPyridineHCID 1049—
ProductHCID 70495615HCID 7049561567%

Reaction Steps

A mixture of 1-ethyl-6-bromo-7-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid 1.65 g, piperazine 2.15 g and pyridine 2 ml was refluxed for 12 hours by heating. The reaction mixture was evaporated under vacuum and dissolved in aqueous acetic acid. The insoluble matters were removed by filtration. The filtrate was neutralized with an aqueous solution of NaOH. The precipitated crystals were collected by filtration and washed with water. The precipitate was recrystallized from a mixed solvent of concentrated hydrochloric acid and ethanol to obtain 1.4 g (67%) of 1-ethyl-6-bromo-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic acid hydrochloride as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-2bf06bfb9dcd4da9a96ccf5fa76a5bba
Source noteuspto-grants-1984_05