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.[CH2:13]([N:15]1[CH:19]=[C:18]([CH2:20][NH:21][C:22]2[CH:27]=[CH:26][C:25]([CH:28]([CH3:30])[CH3:29])=[CH:24][CH:23]=2)[CH:17]=[N:16]1)[CH3:14]>>[CH2:13]([N:15]1[CH:19]=[C:18]([CH2:20][N:21]([C:22]2[CH:23]=[CH:24][C:25]([CH:28]([CH3:29])[CH3:30])=[CH:26][CH:27]=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:17]=[N:16]1)[CH3:14]Komponenten
3
Versuchsvorschrift
By the reaction and treatment in the same manner as in Example 4 using indan-1-carboxylic acid (0.24 g) and [(1-ethylpyrazol-4-yl)methyl](4-isopropylphenyl)amine (0.37 g) as starting materials, N-[(1-ethylpyrazol-4-yl)methyl]-N-(4-isopropylphenyl)indan-1-carboxamide (0.23 g) was obtained. melting point: 83-84° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-177bf9078b2b4bcda9159a1e1b55758e
- Quelldatensatz
- uspto-grants-2012_06
- Patentnummer
- US08198454B2
Verknüpfte Notizen
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