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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614906Generated: October 26, 2026

Piperazine, hexahydrate → 1-Ethyl-6-fluoro-1,4-dihydro-7-(1-piperazinyl)-4-oxoquinoline-3-carboxylic acid pentahydrate

https://huagongshe.com/reaction/614906

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazine, hexahydrateHCID 120181—
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 483169—
SolventWaterHCID 962—
Product1-Ethyl-6-fluoro-1,4-dihydro-7-(1-piperazinyl)-4-oxoquinoline-3-carboxylic acid pentahydrateHCID 70603524—

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 1-ethyl-6-fluoro-7-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.9g), piperazine hexahydrate (15g) and water (15 ml) was heated at 170° C. in a sealed tube for 16 hr. After evaporation of the solvent, the residue was acidified with diluted hydrochloric acid, heated at 100° C., and the hot solution was filtered. The filtrate was evaporated to dryness. The residue was dissolved in 10% sodium hydroxide and neutralized with acetic acid. The precipitate was collected, washed with water, dried, and recrystallized from ethanol to give 1-ethyl-6-fluoro-1,4-dihydro-7-(1-piperazinyl)-4-oxoquinoline-3-carboxylic acid pentahydrate (I) as colorless powder, m.p.: 226°-227° C. Mass spectrum m/e: 319 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04146719
Source datasetuspto-grants-1979_03
ORD IDord-3f951248f3f94041966d29418c103210
Source noteuspto-grants-1979_03