HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610178Generated: October 31, 2026
Piperazine → 1-(6-Amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-4-oxo-7-piperazino-1,4-dihydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/610178
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-(6-Amino-3,5-difluoro-2-pyridinyl)-8-chloro-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid | HCID 15434901 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-Amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-4-oxo-7-piperazino-1,4-dihydroquinoline-3-carboxylic acid | HCID 15486979 | 56.4% |
Reaction Steps
To 170 mg of N,N-dimethylformamide were added 50 mg of 1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, 50 mg of piperazine, and the mixture was stirred at 90° C. for 1 hour. After adding about 0.3 ml of ethanol, the mixture was allowed to cool, and the precipitate was collected by filtration and washed with ethanol and diisopropylether successively to obtain 33 mg of the title compound as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05998436 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-ff2e7d05b64646089c5bdd86307143aa |
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| Source note | uspto-grants-1999_12 |
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