5-Chloro-o-anisic acid → N-(2-Methyl-1,2,3,4-tetrahydroisoquinolin-5-yl)-5-chloro-2-methoxybenzamide
Reaktionsgleichung
[NH2:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][N:6]([CH3:12])[CH2:7]2.[Cl:13][C:14]1[CH:15]=[CH:16][C:17]([O:23][CH3:24])=[C:18]([CH:22]=1)[C:19](O)=[O:20]>>[CH3:12][N:6]1[CH2:5][CH2:4][C:3]2[C:8](=[CH:9][CH:10]=[CH:11][C:2]=2[NH:1][C:19](=[O:20])[C:18]2[CH:22]=[C:14]([Cl:13])[CH:15]=[CH:16][C:17]=2[O:23][CH3:24])[CH2:7]1Komponenten
3
Versuchsvorschrift
The title compound was prepared in an analogous manner to Example 1 from 5-amino-2-methyl-1,2,3,4-tetrahydroisoquinoline and 5-chloro-2-methoxybenzoic acid.
Quellen und Nachweise
- ORD-Eintrag
- ord-09976da0e0ad4a3ea8104760475f825c
- Quelldatensatz
- uspto-grants-2000_08
- Patentnummer
- US06110934