Acetate → 1-(6-Amino-3-fluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Reaktionsgleichung

Cl.C([O-])(=O)C.[F:6][C:7]1[C:8]([N:22]2[C:31]3[C:26](=[CH:27][C:28]([F:34])=[C:29]([F:33])[C:30]=3[Cl:32])[C:25](=[O:35])[C:24]([C:36]([O:38]CC)=[O:37])=[CH:23]2)=[N:9][C:10]([NH:13]C(C)(C)CC(C)(C)C)=[CH:11][CH:12]=1>>[NH2:13][C:10]1[N:9]=[C:8]([N:22]2[C:31]3[C:26](=[CH:27][C:28]([F:34])=[C:29]([F:33])[C:30]=3[Cl:32])[C:25](=[O:35])[C:24]([C:36]([OH:38])=[O:37])=[CH:23]2)[C:7]([F:6])=[CH:12][CH:11]=1

Komponenten

Edukt 3

HCID 175Acetate

HCID 313Hydrochloric Acid

HCID 22121174Ethyl 1-[3-fluoro-6-(1,1,3,3-tetramethylbutylamino)pyridin-2-yl]-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Produkt 1

HCID 221212881-(6-Amino-3-fluoropyridin-2-yl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidAusbeute 85,1 %

Versuchsvorschrift

To 1.2 ml of the mixed solution of 4N hydrochloric acid and acetate (1:1) was added 235 mg of ethyl 1-[3-fluoro-6-(1,1,3,3-tetramethylbutylamino)pyridine-2-yl]-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate and the mixture was heated under reflux for 6 hours with stirring and allowed to cool. The precipitate was collected by filtration and washed with ethanol to obtain 145 mg of the title compound as a gray powder.