Reaktionsgleichung
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:9][NH2:10])=[C:6]([OH:8])[CH:7]=1.CC1C=CC(S([O-])(=O)=O)=CC=1.[Cl:22][CH:23]([C:27](=O)[CH3:28])[C:24](=O)[CH3:25]>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([N:9]2[C:27]([CH3:28])=[C:23]([Cl:22])[C:24]([CH3:25])=[N:10]2)=[C:6]([OH:8])[CH:7]=1Komponenten
3
Versuchsvorschrift
558 mg of the title compound was prepared in a manner similar to Example 54b) by using 5-bromo-2-hydrazinylphenol 4-methylbenzenesulfonate (0.9 g), which was prepared in a manner similar to Example 54a), and 3-chloropentane-2,4-dione (1.07 g).
Quellen und Nachweise
- ORD-Eintrag
- ord-ba2008632ec146f8b3539f6a2856b17f
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08889727B2
Verknüpfte Notizen
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