HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330087Generated: October 29, 2026
Piperazine → 7-(1-Piperazinyl)-1-cyclopropyl-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid
https://huagongshe.com/reaction/330087
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1-Cyclopropyl-6,7-difluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 14052575 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-(1-Piperazinyl)-1-cyclopropyl-6-fluoro-8-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid | HCID 14052580 | 18.6% |
Reaction Steps
A mixture of 1-cyclopropyl-6,7-difluoro-1,4-dihydro-8-methyl-4-oxo-3-quinolinecarboxylic acid (200 mg), piperazine (250 mg) in anhydrous DMSO (2 ml) was stirred at 70° to 80° C. for 4 hours. After the reacting mixture was concentrated under reduced pressure, to the resulting residue was added methanol and the resulting precipitate was filtered off. After the filtrate was concentrated under reduced pressure, the resulting residue was purified by silica gel column chromatography eluting chloroform-methanol (20:1) chloroform-methanol-concentrated aqueous ammonia (10:10:1) and further purified by preparative thin layer chromatography eluting chloroform-methanol (20:1)→chloroform methanol-concentrated aqueous ammonia (10:10:1→10:10:3) to give the title compound (46 mg) as redish powder, mp 300° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04894458 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-9095eeae03ed4e128a5d4317d30748c6 |
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| Source note | uspto-grants-1990_01 |
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