Reaktionsgleichung
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:15]([CH2:16][CH2:17][CH2:18][O:19][CH3:20])[C:14]3[CH:21]=[C:22]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][C:31](OC)=[O:32])[CH:23]=[CH:24][C:13]=3[N:12]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[CH3:35][O:36][CH2:37][CH2:38][CH2:39][NH2:40]>>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[N:15]([CH2:16][CH2:17][CH2:18][O:19][CH3:20])[C:14]3[CH:21]=[C:22]([O:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][C:31]([NH:40][CH2:39][CH2:38][CH2:37][O:36][CH3:35])=[O:32])[CH:23]=[CH:24][C:13]=3[N:12]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Komponenten
3
Versuchsvorschrift
2-(4-tert-Butyl-phenyl)-6-[(5-(methoxycarbonyl)pentyl)oxy]-1-(3-methoxy-propyl)-benzimidazole is reacted with 3-methoxypropylamine according to general operating instructions 7. 2-(4-tert-Butyl-phenyl)-1-(3-methoxy-propyl)-6-[(5-((3-methoxy-propyl)amino-carbonyl)-pentyl)oxy]-benzimidazole is obtained as a yellow solid.
Quellen und Nachweise
- ORD-Eintrag
- ord-25c4ec6eeff645969075f65bd48d134b
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06855714B2
Verknüpfte Notizen
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