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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544219Generated: October 26, 2026

Piperazine → HCID 12733904, compound

https://huagongshe.com/reaction/544219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-(2-Fluoroethyl)-6-fluoro-7-chloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 12733880—
SolventPyridineHCID 1049—
ProductHCID 12733904HCID 1273390427%

Reaction Steps

A mixture of 1-(2-fluoroethyl)-6-fluoro-7-chloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (0.87 g) (3 millimole), piperazine (1.3 g) (15 millimole) and pyridine (4 ml) piperazine was heated at 135° to 145° C. for 12 hours. After cooling, the reaction mixture was evaporated under vacuum, the residue was acidified with acetic acid, the undissolved matter was filtered off. The filtrate was neutralized in an aqueous solution of caustic soda. The precipitate was filtered, washed, dried and dissolved in diluted HCl. Ethanol was added and the solution was ice cooled. The precipitate was filtered, washed with ethanol and dried and recrystallized from ethanol to obtain 0.30 g (27%) of 1-(2-fluoroethyl)-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid hydrochloride in powder form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-8b333a19b7424aac81f98f6775d506ab
Source noteuspto-grants-1984_05