Reaktionsgleichung
[Cl:1][CH2:2][CH2:3][CH2:4][N:5]=[C:6]=[O:7].CO[C:10]([C@:12]1([CH3:34])[CH2:24][C:23]2[C:22]3[C:17](=[CH:18][CH:19]=[C:20]([O:25][CH3:26])[CH:21]=3)[NH:16][C:15]=2[C@@H:14]([C:27]2[CH:32]=[CH:31][CH:30]=[C:29]([OH:33])[CH:28]=2)[NH:13]1)=[O:11]>>[Cl:1][CH2:2][CH2:3][CH2:4][N:5]1[C:6](=[O:7])[N:13]2[C@H:14]([C:27]3[CH:32]=[CH:31][CH:30]=[C:29]([OH:33])[CH:28]=3)[C:15]3[NH:16][C:17]4[C:22]([C:23]=3[CH2:24][C@@:12]2([CH3:34])[C:10]1=[O:11])=[CH:21][C:20]([O:25][CH3:26])=[CH:19][CH:18]=4Komponenten
3
Versuchsvorschrift
The title compound is prepared analogously to the procedure described for example 22, using chloro propyl isocyanate and (1R,3S)-1-(3-hydroxy-phenyl)-6-methoxy-3-methyl-2,3,4,9-tetrahydro-1H-β-carboline-3-carboxylic acid methyl ester. MS: m/z (MH+)=454.0
Quellen und Nachweise
- ORD-Eintrag
- ord-ac94f9d981c3429680d2d0e9382e51b1
- Quelldatensatz
- uspto-grants-2013_09
- Patentnummer
- US08530493B2
Verknüpfte Notizen
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