Reaktionsgleichung
[NH2:1][C@H:2]([C:10]([NH:12][CH2:13][CH2:14][N:15]([CH3:17])[CH3:16])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.C(N[S:22]([C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[NH:30][C:29](=[O:34])[C:28]2=[O:35])(=[O:24])=[O:23])CC>>[CH3:17][N:15]([CH3:16])[CH2:14][CH2:13][NH:12][C:10](=[O:11])[C@@H:2]([NH:1][S:22]([C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[NH:30][C:29](=[O:34])[C:28]2=[O:35])(=[O:23])=[O:24])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1Komponenten
3
Versuchsvorschrift
The title compound was prepared from L-Phe-NHCH2CH2NMe2 following the procedure for 2,3-Dioxo-2,3-dihydro-1H-indole-5-sulfonic acid propylamide.
Quellen und Nachweise
- ORD-Eintrag
- ord-f5071689e4304ddcbff53d9dadc70138
- Quelldatensatz
- uspto-grants-2014_10
- Patentnummer
- US08871718B2
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