HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368429Generated: October 27, 2026
Dimethylformamide → 7-(3-Aminoazetidin-1-yl)-1-(4-amino-5-fluoropyrimidin-2-yl)-8-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
https://huagongshe.com/reaction/368429
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | Azetidin-3-amine--hydrogen chloride (1/2) | HCID 13491919 | — |
| Reactant | 1-(4-Amino-5-fluoropyrimidine-2-yl)-8-chloro 6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121195 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-(3-Aminoazetidin-1-yl)-1-(4-amino-5-fluoropyrimidin-2-yl)-8-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 22121169 | 35.1% |
Reaction Steps
To 100 mg of N,N-dimethylformamide were added 25 mg of 1-(4-amino-5-fluoropyrimidine-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, 20 mg of 3-aminoazetidine dihydrochloride, and 50 mg of N-methylpyrrolidine, and the mixture was stirred at 90° C. for 1 hour. After adding 0.2 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 10 mg of the title compound as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133284 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-da5f4c12e08f4eb1b37101d7e44480ea |
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| Source note | uspto-grants-2000_10 |
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