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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050635Generated: November 1, 2026

5-Benzylamino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid → 7-(4-Acetyl-3-methyl-1-piperazinyl)-5-benzylamino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid

https://huagongshe.com/reaction/2050635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzylamino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 14880208—
Reactant1-(2-Methylpiperazin-1-yl)ethan-1-oneHCID 15729409—
SolventPyridineHCID 1049—
Product7-(4-Acetyl-3-methyl-1-piperazinyl)-5-benzylamino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 19810621—

Reaction Steps

A mixture of 5-benzylamino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 1-acetyl-2-methylpiperazine and pyridine was heated under reflux. The reaction mixture was concentrated under reduced pressure, and water was added to the residue. The mixture was extracted with chloroform. The extract was dried and chloroform was evaporated. Ethanol was added to the residue, and the crystals were collected by filtration to give 7-(4-acetyl-3-methyl-1-piperazinyl)-5-benzylamino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid. It was recrystallized from ethanol/diisopropyl ether. m.p. 235°-236° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013841
Source datasetuspto-grants-1991_05
ORD IDord-46b813fa20dc479887f1f5098ac59245
Source noteuspto-grants-1991_05