Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580449Generated: October 30, 2026

1-Methylpiperazine → HCID 70416203, compound

https://huagongshe.com/reaction/580449

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 20133864HCID 20133864—
SolventEthanolHCID 702—
ProductHCID 70416203HCID 7041620387.8%

Reaction Steps

3 g of 1-methylpiperazine are added dropwise to a suspension of 2.53 g of 1-methylamino-7-chloro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid in 30 ml of ethanol, with stirring, the acid dissolving in a slightly exothermic reaction. The mixture is heated at the boiling point for 1 hour, the ethanol is distilled off and the reaction product is dissolved in 1N sodium hydroxide solution. The filtered solution is brought to pH 6 with 10% strength hydrochloric acid. The precipitate is filtered off in the cold, washed with a little cold water and ethanol and dried in vacuo at 80° C. 3.1 g of 1-methylamino-7-(4-methyl-1-piperazinyl)-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid hydrochloride of decomposition point 328° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753925
Source datasetuspto-grants-1988_06
ORD IDord-0702808ebfbd42b0aa0aa153a5a214f7
Source noteuspto-grants-1988_06