HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235040Generated: October 31, 2026
1-Methylpyrrolidine → HCID 68439913, compound
https://huagongshe.com/reaction/2235040
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpyrrolidine | HCID 8454 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 15486977 | — |
| Reactant | N-(Propan-2-yl)azetidin-3-amine--hydrogen chloride (1/2) | HCID 53439424 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 68439913 | HCID 68439913 | 65% |
Reaction Steps
N-isopropylazetidin-3-ylamine dihydrochloride (374 mg), 1-(6-amino-3,5-difluoropyridin-2-yl)-8-bromo-6,7-difluoro-4-oxo-1,4-dihydroquinolin-3-carboxylic acid (518 mg), N-methylpyrrolidine (0.8 mL), lithium chloride (500 mg) and dimethyl sulfoxide (1.5 mL) were mixed, and the mixture was stirred at 50° C. for 4.5 hours. After the mixture had been left to cool, diethyl ether (10 mL) was added to the mixture and stirred, followed by removing the supernatant. The same procedure was repeated three times. Water (3 mL) was added to the residue, and the pH of the mixture was adjusted to 6 by use of aqueous citric acid solution. The formed solid was collected through filtration, washed three times with water (3 mL), then suspended in ethanol (10 mL), and stirred under heating. The formed solid was collected through filtration, and suspended in diisopropyl ether (10 mL), followed by stirring under heating. The heated suspension was filtrated to yield 410 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713997B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-52d1a787340c40adbfe86f3846b88daf |
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| Source note | uspto-grants-2010_05 |
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