Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:16]3[C:11](=[N:12][CH:13]=[CH:14][CH:15]=3)[NH:10][C:9]=2[C:17]([NH2:19])=[O:18])=[CH:4][CH:3]=1.[F:20][C:21]1[CH:22]=[C:23]([N:31]=[C:32]=[O:33])[CH:24]=[C:25]([C:27]([F:30])([F:29])[F:28])[CH:26]=1>>[F:20][C:21]1[CH:22]=[C:23]([NH:31][C:32](=[O:33])[NH:1][C:2]2[CH:3]=[CH:4][C:5]([C:8]3[C:16]4[C:11](=[N:12][CH:13]=[CH:14][CH:15]=4)[NH:10][C:9]=3[C:17]([NH2:19])=[O:18])=[CH:6][CH:7]=2)[CH:24]=[C:25]([C:27]([F:29])([F:30])[F:28])[CH:26]=1Komponenten
3
Versuchsvorschrift
78.1 mg of solid beige-coloured 3-{4-[3-(3-fluoro-5-trifluoromethylphenyl)-ureido]phenyl}-1H-pyrrolo[2,3-b]pyridine-2-carboxamide are prepared as described in Example 7 starting with 3-(4-aminophenyl)-1H-pyrrolo[2,3-b]-pyridine-2-carboxamide and 3-fluoro-5-trifluoromethylphenyl isocyanate.
Quellen und Nachweise
- ORD-Eintrag
- ord-e5bf14c41b3c42fdb2f88a07c9111810
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07947706B2
Verknüpfte Notizen
Wird geladen…