Methylamine → HCID 69958909, Verbindung
Reaktionsgleichung
[Cl:1][C:2]1[C:3](F)=[C:4]([F:26])[CH:5]=[C:6]2[C:11]=1[N:10]([C:12]1[CH:17]=[C:16]([NH:18][CH3:19])[C:15]([F:20])=[CH:14][C:13]=1[F:21])[CH:9]=[C:8]([C:22]([OH:24])=[O:23])[C:7]2=[O:25].[CH3:28][NH2:29]>N1C=CC=CC=1>[CH3:9][NH2:10].[Cl:1][C:2]1[C:3]([NH:29][CH3:28])=[C:4]([F:26])[CH:5]=[C:6]2[C:11]=1[N:10]([C:12]1[CH:17]=[C:16]([NH:18][CH3:19])[C:15]([F:20])=[CH:14][C:13]=1[F:21])[CH:9]=[C:8]([C:22]([OH:24])=[O:23])[C:7]2=[O:25]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
8-Chloro-6,7-difluoro-1-(2,4-difluoro-5-methylaminophenyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (200 mg) and a 40% aqueous solution (220 mg) of methylamine were added to pyridine (600 mg), and the mixture was stirred at room temperature for 5 hours. After the solvent was distilled off under reduced pressure, ethanol (1 ml) was added to the residue, and the mixture was stirred for 30 minutes. Deposits were collected by filtration and washed successively with ethanol and diisopropyl ether to obtain the title compound (92 mg) as a colorless powder.