Reaktionsgleichung
[CH3:1][C:2]1([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:5](=[O:6])[CH2:4][C:3]1=[O:7].[CH:14](=O)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[F:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[NH:28][CH:27]=[C:26]2[CH3:32]>>[F:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[NH:28][C:27]([CH:14]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:4]1[C:3](=[O:7])[C:2]([CH3:1])([C:8]3[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:5]=1[OH:6])=[C:26]2[CH3:32]Komponenten
4
Versuchsvorschrift
Using general procedure C, 2-methyl-2-phenyl-cyclobutane-1,3-dione (Lit. 1) was reacted with benzaldehyde and 5-fluoro-3-methyl-1H-indole to give the title compound as a colorless solid. MS: 410.3 ([M−H]−).
Quellen und Nachweise
- ORD-Eintrag
- ord-d1ab97c69cc84845a555228cf8864fce
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07705034B2
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