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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084352Generated: October 30, 2026

2-Methylpiperazine → HCID 14700559, compound

https://huagongshe.com/reaction/1084352

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylpiperazineHCID 66057—
Reactant8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acidHCID 14700554—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
SolventPotassium HydroxideHCID 14797—
ProductHCID 14700559HCID 1470055963.9%

Reaction Steps

A suspension of 3.5 g of 8-chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine-3-carboxylic acid and 4.6 g of 2-methylpiperazine in 40 cm3 of pyridine is heated at a temperature close to 115° C., with stirring, for 13 hours. The reaction mixture is concentrated to dryness under reduced pressure (20 kPa) at 60° C. The residue is twice taken up with 30 cm3 of ethanol and concentrated under reduced pressure under the above conditions. The solid obtained is taken up in 60 cm3 of water and 10 cm3 of 30% aqueous potassium hydroxide solution. The aqueous phase is washed with twice 100 cm3 of trichloromethane, 10.28 g of methanesulphonic acid are added and the aqueous phase is again washed with twice 100 cm3 of trichloromethane. 10 cm3 of 30% aqueous potassium hydroxide solution are added. The precipitate formed is drained and washed with 3 times 10 cm3 of water and twice 10 cm3 of ethanol. 2.7 g of 7-fluoro-1-methyl-8-(3-methyl-1-piperazinyl)-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid are obtained in the form of a yellow solid melting at 360°-363° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05004745
Source datasetuspto-grants-1991_04
ORD IDord-3814fbe0521f4a28b6cd9ee4e5de97a6
Source noteuspto-grants-1991_04