Ethanol → HCID 68439912, Verbindung
Reaktionsgleichung
[NH2:1][C:2]1[N:7]=[C:6]([N:8]2[C:17]3[C:12](=[CH:13][C:14]([F:27])=[C:15]([N:19]4[CH2:22][CH:21]([NH:23][CH:24]([CH3:26])[CH3:25])[CH2:20]4)[C:16]=3[Br:18])[C:11](=[O:28])[C:10]([C:29]([OH:31])=[O:30])=[CH:9]2)[C:5]([F:32])=[CH:4][C:3]=1[F:33].[C:34]([OH:41])(=[O:40])/[CH:35]=[CH:36]\[C:37]([OH:39])=[O:38].C(O)C>O>[C:34]([OH:41])(=[O:40])/[CH:35]=[CH:36]\[C:37]([OH:39])=[O:38].[NH2:1][C:2]1[N:7]=[C:6]([N:8]2[C:17]3[C:12](=[CH:13][C:14]([F:27])=[C:15]([N:19]4[CH2:20][CH:21]([NH:23][CH:24]([CH3:26])[CH3:25])[CH2:22]4)[C:16]=3[Br:18])[C:11](=[O:28])[C:10]([C:29]([OH:31])=[O:30])=[CH:9]2)[C:5]([F:32])=[CH:4][C:3]=1[F:33]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 80 °C
Versuchsvorschrift
1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6-fluoro-7-(3-isopropylaminoazetidin-1-yl)-4-oxo-1,4-dihydroquinolin-3-carboxylic acid (132 mg) and maleic acid (58 mg) were added to ethanol (3 mL), and the mixture was heated at 80° C. Water was gradually added to the mixture until the compounds were completely dissolved. After the solution had been left to cool, the formed solid was collected through filtration, to thereby yield 102 mg of the title compound.
Aufarbeitung
- dissolutionwere completely dissolved
- waitAfter the solution had been left
- temperatureto cool
- filtrationthe formed solid was collected through filtration
Quellen und Nachweise
- ORD-Eintrag
- ord-31725629c7b4403c8215b20a560bee53
- Quelldatensatz
- uspto-grants-2010_05
- Patentnummer
- US07713997B2
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