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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235040Generated: October 31, 2026

1-Methylpyrrolidine → HCID 68439913, compound

https://huagongshe.com/reaction/2235040

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpyrrolidineHCID 8454—
ReactantLithium ChlorideHCID 433294—
Reactant1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 15486977—
ReactantN-(Propan-2-yl)azetidin-3-amine--hydrogen chloride (1/2)HCID 53439424—
SolventDimethyl SulfoxideHCID 679—
SolventDiethyl EtherHCID 3283—
ProductHCID 68439913HCID 6843991365%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713997B2
Source datasetuspto-grants-2010_05
ORD IDord-52d1a787340c40adbfe86f3846b88daf
Source noteuspto-grants-2010_05