Reaktionsgleichung
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:25]#[N:26])=[C:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][N:11]([CH:16]([CH2:20][CH2:21][O:22][CH3:23])[C:17]([OH:19])=O)[C:10](=[O:24])[CH:9]=2)[CH:7]=1.[NH2:27][C:28]1[CH:36]=[C:35]2[C:31]([C:32](=[O:37])[NH:33][NH:34]2)=[CH:30][CH:29]=1>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:25]#[N:26])=[C:6]([C:8]2[C:13]([O:14][CH3:15])=[CH:12][N:11]([CH:16]([CH2:20][CH2:21][O:22][CH3:23])[C:17]([NH:27][C:28]3[CH:36]=[C:35]4[C:31]([C:32](=[O:37])[NH:33][NH:34]4)=[CH:30][CH:29]=3)=[O:19])[C:10](=[O:24])[CH:9]=2)[CH:7]=1Komponenten
3
Versuchsvorschrift
150 mg (377 μmol) of 2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4-methoxybutanoic acid (racemate) and 65 mg (438 μmol, 1.1 eq.) of 6-amino-1H-indazol-3(2H)-one were reacted according to General Method 1. The crude product was purified by flash chromatography (silica gel 50, dichloromethane/methanol mixtures). Yield: 105 mg (52% of theory)
Aufarbeitung
- customThe crude product was purified by flash chromatography (silica gel 50, dichloromethane/methanol mixtures)
Quellen und Nachweise
- ORD-Eintrag
- ord-0d272ada47164648ba809b68862f9443
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09434690B2
Verknüpfte Notizen
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