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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165605Generated: October 26, 2026

7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid → 1-Ethyl-6-fluoro 1,4-dihydro-7-[3-[(4-methyl-1-piperazinyl)methyl]-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/2165605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 483169—
Reactant1-Methyl-4-(2-piperazinylmethyl)piperazineHCID 19763560—
SolventPyridineHCID 1049—
Product1-Ethyl-6-fluoro 1,4-dihydro-7-[3-[(4-methyl-1-piperazinyl)methyl]-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acidHCID 19763596—

Reaction Steps

A 425 mg portion of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid and 1.25 g of 1-methyl-4-(2-piperazinylmethyl)piperazine were suspended in 5 ml of pyridine and heated at reflux, under argon, for 18 hours. The solvents were removed and the residue evaporated twice from toluene. The residue was dissolved in dichloromethane, hexane was added, the resulting gum was separated, dissolved in dichloromethane and filtered. Ether was added to the filtrate, the resulting solid collected and recyrstallized, giving 360 mg of the desired product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04940710
Source datasetuspto-grants-1990_07
ORD IDord-6bdebb9193ab43e0a84ac4b96aef7121
Source noteuspto-grants-1990_07