HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610292Generated: November 2, 2026
Pyridine → 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-methylaminoazetidin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/610292
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121165 | — |
| Reactant | 3-Methylaminoazetidine diacetate | HCID 86754914 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-Amino-1-(6-amino-3,5-difluoropyridin-2-yl)-8-chloro-6-fluoro-7-(3-methylaminoazetidin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121251 | 51.5% |
Reaction Steps
To 300 mg of pyridine were added 120 mg of 5-amino-1-(6-amino-3 , 5-difluoropyridin-2-yl) -8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, 80 mg of 3-methylaminoazetidine diacetate, and 250 mg of N-methylpyrrolidine, and the mixture was stirred at 100° C. for 10 minutes. After adding 5 ml of diethylether, the mixture was stirred and allowed to cool for 1 hour, and decanted. 2 ml of ethanol was added and the mixture was stirred. The precipitate was collected by filtration and washed with ethanol and diethylether successively to obtain 72 mg of the title compound as a yellow 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-18af41378b07451b8242d6699cb8b0c3 |
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| Source note | uspto-grants-1999_12 |
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