Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]2[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[CH:12][CH:11]=2)=[O:9])=[CH:4][CH:3]=1.CN1C(C(C2C=CC([N+]([O-])=O)=CC=2)=O)=CN=C1.N1(C2C=CC(CC3C(OC)=NC4C(C=3Cl)=CC(Br)=CC=4C)=CC=2)C=CC=N1>>[NH2:16][C:13]1[CH:14]=[CH:15][C:10]([C:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)=[O:9])=[CH:11][CH:12]=1Komponenten
4
Versuchsvorschrift
The title compound was prepared by using (4-chlorophenyl)(4-nitrophenyl)methanone, (Intermediate 21: step a) in place of (1-methyl-1H-imidazol-5-yl)(4-nitrophenyl)methanone, (Intermediate 20: step b) then following the procedure described for the preparation of (4-aminophenyl)(1-methyl-1H-imidazol-5-yl)methanone (Intermediate 20: step c).
Quellen und Nachweise
- ORD-Eintrag
- ord-f6561176840b424bb343c00588ed5a52
- Quelldatensatz
- uspto-grants-2016_03
- Patentnummer
- US09290476B2
Verknüpfte Notizen
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