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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544222Generated: November 3, 2026

1-Methylpiperazine → HCID 12733914, compound

https://huagongshe.com/reaction/544222

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant6,7-Dichloro-1-ethyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 12733886—
SolventWaterHCID 962—
ProductHCID 12733914HCID 1273391430%

Reaction Steps

A mixture of 1-ethyl-6,7-dichloro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid 2.86 g (0.01 mole), N-methylpiperazine 10 g (0.1 mole) and 15 ml water was heated in a sealed tube at 125°-130° C. (inner temperature) for 19 hours. After cooling, the reaction mixture was evaporated under vacuum and acidified with acetic acid. Insoluble matters were filtered off and the filtrate was neutralized with an aqueous solutiong of NaOH to pH 7, extracted with CHCl3, dried with anhydrous Na2SO4, and the solvent was distilled off. The residue was recrystallized from a mixed solvent of CHCl3 and benzene to give 1.05 g (30%) of 1-ethyl-6-chloro-7-(4-methyl-1-piperazinyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid. Colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-acaa4dd7379e47b2a113b4193cc44c09
Source noteuspto-grants-1984_05