Reaktionsgleichung
[CH2:1]([O:3][C:4]([C:6]1([C:11]2[CH:16]=[CH:15][C:14]([CH2:17]Br)=[CH:13][N:12]=2)[CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5])[CH3:2].[CH:19]1([C:22]2[NH:23][C:24]3[C:25]([N:32]=2)=[N:26][C:27]([CH3:31])=[CH:28][C:29]=3[CH3:30])[CH2:21][CH2:20]1>>[CH2:1]([O:3][C:4]([C:6]1([C:11]2[CH:16]=[CH:15][C:14]([CH2:17][N:32]3[C:25]4=[N:26][C:27]([CH3:31])=[CH:28][C:29]([CH3:30])=[C:24]4[N:23]=[C:22]3[CH:19]3[CH2:21][CH2:20]3)=[CH:13][N:12]=2)[CH2:10][CH2:9][CH2:8][CH2:7]1)=[O:5])[CH3:2]Komponenten
3
Versuchsvorschrift
The product of Example 10, Step 3, above (45), was alkylated as described in Example 1, Step 5, using 2-cyclopropyl-5,7-dimethylimidazo[4,5-b]pyridine (13) to produce the title compound (48).
Quellen und Nachweise
- ORD-Eintrag
- ord-d9823b0750f84d649baf30be4e65a122
- Quelldatensatz
- uspto-grants-1998_08
- Patentnummer
- US05789415
Verknüpfte Notizen
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