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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544214Generated: November 2, 2026

Norfloxacin → 1-Ethyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/544214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNorfloxacinHCID 4539—
ReactantTriethylamineHCID 8471—
SolventDimethylformamideHCID 6228—
Product1-Ethyl-7-(4-ethyl-1-piperazinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 46593172%

Reaction Steps

A mixture of 1-ethyl-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid (0.96 g) (3 millimole), iodoethyl (0.94 g) (6 millimole), triethylamine (0.6 g) (6 millimole) and 10 ml DMF was heated to 70° to 80° C. for 2.5 hours under stirring. After cooling, the reaction mixture was evaporated under vacuum and the residue was dissolved in dichloromethane, washed with water, dried over anhydrous Na2SO4 and the solvent was removed. The residue was recrystallized from a mixture of CHCl3 and benzene to obtain 0.75 g (72%) of 1-ethyl-6-fluoro-7-(4-ethyl-1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-a5e0daca0ec14fb9b7e774b7f7eeeb24
Source noteuspto-grants-1984_05