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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050633Generated: November 1, 2026

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

https://huagongshe.com/reaction/2050633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 14880209—
Reactant1-(2-Methylpiperazin-1-yl)ethan-1-oneHCID 15729409—
SolventPyridineHCID 1049—
Product7-(4-Acetyl-3-methyl-1-piperazinyl)-5-amino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 15729410—

Reaction Steps

A mixture of 5-amino-1-cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 1-acetyl-2-methylpiperazine and pyridine was heated under reflux for 5 hours. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in aqueous ammonia. The solution was neutralized with an aqueous solution of acetic acid and cooled with ice. The crystals were collected by filtration to give 7-(4-acetyl-3-methyl-1-piperazinyl)-5-amino-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid. It was recrystallized from ethanol/chloroform. m.p. 269°-271° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05013841
Source datasetuspto-grants-1991_05
ORD IDord-a254543fe26e44dab0c232017bc3e6fd
Source noteuspto-grants-1991_05