HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477013Generated: October 29, 2026
1-Piperazinecarboxaldehyde → HCID 14304585, compound
https://huagongshe.com/reaction/477013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | 1-Cyclopropyl-5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 13825515 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 14304585 | HCID 14304585 | 60.8% |
Reaction Steps
A mixture of 1-cyclopropyl-5,6,7,8-tetrafluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (2.0 g), 4-formylpiperazine (0.75 g), and pyridine (30 ml) was stirred at 50° C. for 1 hour. The reaction mixture was concentrated to dryness under reduced pressure. The residue was mixed with water and extracted with chloroform. The extract was dried, and chloroform was evaporated. Ethanol was added to the residue, and the precipitated crystals were collected by filtration. Recrystallization from chloroform-ethanol gave 1-cyclopropyl-5,6,8-trifluoro-7-(4-formyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.58 g), m.p. 290°-297° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04886810 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-0a3cfa4dd6f54e39beac71158c90bb25 |
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| Source note | uspto-grants-1989_12 |
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