Reaktionsgleichung
[CH:1]1([C:10]([OH:12])=O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[CH3:13][N:14]([CH3:31])[C:15]1[CH:20]=[CH:19][C:18]([CH2:21][NH:22][C:23]2[CH:28]=[CH:27][C:26]([CH2:29][CH3:30])=[CH:25][CH:24]=2)=[CH:17][CH:16]=1>>[CH3:13][N:14]([CH3:31])[C:15]1[CH:16]=[CH:17][C:18]([CH2:21][N:22]([C:23]2[CH:28]=[CH:27][C:26]([CH2:29][CH3:30])=[CH:25][CH:24]=2)[C:10]([CH:1]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[CH2:3][CH2:2]2)=[O:12])=[CH:19][CH:20]=1Komponenten
3
Versuchsvorschrift
By the reaction and treatment in the same manner as in Example 1 using indan-1-carboxylic acid (0.46 g) and [(4-dimethylaminophenyl)methyl](4-ethylphenyl)amine (0.6 g) as starting materials, N-[(4-dimethylaminophenyl) methyl]-N-(4-ethylphenyl)indan-1-carboxamide (0.15 g) was obtained.
Quellen und Nachweise
- ORD-Eintrag
- ord-15cad15a89664cc3ba01dc11fc765d53
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08198454B2
Verknüpfte Notizen
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