HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580449Generated: October 30, 2026
1-Methylpiperazine → HCID 70416203, compound
https://huagongshe.com/reaction/580449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 20133864 | HCID 20133864 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 70416203 | HCID 70416203 | 87.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753925 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-0702808ebfbd42b0aa0aa153a5a214f7 |
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| Source note | uspto-grants-1988_06 |
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