Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[C:15]([OH:18])[CH:16]=3)[N:11]([CH2:19][CH2:20][CH3:21])[C:10]=2[CH3:22])=[CH:5][CH:4]=1.[CH2:23]([O:25][C:26](=[O:31])[C:27](Br)([CH3:29])[CH3:28])[CH3:24]>>[CH2:23]([O:25][C:26](=[O:31])[C:27]([O:18][C:15]1[CH:16]=[C:17]2[C:12](=[CH:13][CH:14]=1)[N:11]([CH2:19][CH2:20][CH3:21])[C:10]([CH3:22])=[C:9]2[C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)([CH3:29])[CH3:28])[CH3:24]Komponenten
3
Versuchsvorschrift
In accordance with the procedure of Example 10, the above compound was prepared from 3-(4-methoxy-phenyl)-2-methyl-1-propyl-1H-indole-5-ol and 2-bromo-2-methyl-propanoic acid ethylester.
Quellen und Nachweise
- ORD-Eintrag
- ord-bf3f4e20a942408a9ab8a735c01e3ded
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04343811
Verknüpfte Notizen
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