Reaktionsgleichung
[NH2:1][C:2]1[C:7]([C:8]([OH:10])=O)=[CH:6][C:5]([O:11][CH3:12])=[N:4][CH:3]=1.[CH3:13][NH2:14].[CH:15]1([N:20]2[CH2:25][CH2:24][CH:23]([O:26][C:27]3[CH:34]=[CH:33][C:30]([CH:31]=O)=[CH:29][CH:28]=3)[CH2:22][CH2:21]2)[CH2:19][CH2:18][CH2:17][CH2:16]1>>[CH:15]1([N:20]2[CH2:25][CH2:24][CH:23]([O:26][C:27]3[CH:34]=[CH:33][C:30]([C:31]4[N:14]([CH3:13])[C:8](=[O:10])[C:7]5[CH:6]=[C:5]([O:11][CH3:12])[N:4]=[CH:3][C:2]=5[N:1]=4)=[CH:29][CH:28]=3)[CH2:22][CH2:21]2)[CH2:19][CH2:18][CH2:17][CH2:16]1Komponenten
4
Versuchsvorschrift
The entitled compound was obtained according to the method of Example 15 but starting from 5-amino-2-methoxyisonicotinic acid, methylamine and 4-[(1-cyclopentyl-4-piperidinyl)oxy]benzaldehyde.
Aufarbeitung
- customThe entitled compound was obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-a631bf5edc344b8188a6eb0996cbf6b3
- Quelldatensatz
- uspto-grants-2011_06
- Patentnummer
- US07960394B2
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