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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544232Generated: October 30, 2026

Piperazine → HCID 70495429, compound

https://huagongshe.com/reaction/544232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 12733883HCID 12733883—
SolventPyridineHCID 1049—
ProductHCID 70495429HCID 7049542926.1%

Reaction Steps

A mixture of 1-allyl-6-fluoro-7-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid 0.94 g, piperazine 2.9 g and 2 ml of pyridine was refluxed for 8 hours by heating. After cooling, the reaction mixture was evaporated under vacuum. The residue was dissolved in an aqueous solution of acetic acid and the insoluble matters were removed by filtration. The filtrate was neutralized with an aqueous solution of NaOH. The precipitated crystals were collected by filtration, washed with water and dried. Recrystallizing the crystals from a mixed solvent of concentrated hydrochloric acid and ethanol, 0.32 g (26%) of 1-allyl-6-fluoro-1,4-dihydro-4-oxo-(1-piperazinyl)-quinoline-3-carboxylic acid hydrochloride was obtained. Colorless powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-7600cdb8ef0d4da8b970c72fb0d66730
Source noteuspto-grants-1984_05