HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 70495429, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 12733883 | HCID 12733883 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 70495429 | HCID 70495429 | 26.1% |
Reaction Steps
A mixture of 1-allyl-6-fluoro-7-chloro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid 0.94 g, piperazine 2.9 g and 2 ml of pyridine was refluxed for 8 hours by heating. After cooling, the reaction mixture was evaporated under vacuum. The residue was dissolved in an aqueous solution of acetic acid and the insoluble matters were removed by filtration. The filtrate was neutralized with an aqueous solution of NaOH. The precipitated crystals were collected by filtration, washed with water and dried. Recrystallizing the crystals from a mixed solvent of concentrated hydrochloric acid and ethanol, 0.32 g (26%) of 1-allyl-6-fluoro-1,4-dihydro-4-oxo-(1-piperazinyl)-quinoline-3-carboxylic acid hydrochloride was obtained. Colorless powders.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04448962 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-7600cdb8ef0d4da8b970c72fb0d66730 |
| Source note | uspto-grants-1984_05 |