Reaktionsgleichung
[CH:1]1[C:6]2[NH:7][C:8]3[C:13]([C:5]=2[CH:4]=[C:3]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[N:2]=1)=[CH:12][CH:11]=[CH:10][CH:9]=3.[O:19]([CH2:26][CH:27]1[CH2:29][O:28]1)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[OH:28][CH:27]([CH2:26][O:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[CH2:29][N:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[C:5]2[CH:4]=[C:3]([C:14]([O:16][CH2:17][CH3:18])=[O:15])[N:2]=[CH:1][C:6]1=2Komponenten
3
Versuchsvorschrift
Following Representative Procedure 1, the title compound ethyl 9-(2-hydroxy-3-phenoxypropyl)-9H-pyrido[3,4-b]indole-3-carboxylate was prepared from Ethyl 9H-pyrido[3,4-b]indole-3-carboxylate and phenoxymethyloxirane in 67% yield.
Quellen und Nachweise
- ORD-Eintrag
- ord-df7c4f07954f4a219baccdee9103b33d
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08877797B2
Verknüpfte Notizen
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