Reaktionsgleichung
C[O:2][CH2:3][CH:4]1C[CH2:8][CH2:7][CH2:6][N:5]1[C:10]1[N:15]=[CH:14][N:13]=[C:12]([NH:16][C:17]2[CH:18]=[C:19]([CH2:23][S:24]([NH2:27])(=[O:26])=[O:25])[CH:20]=[CH:21][CH:22]=2)[N:11]=1.ClC1N=CN=C(NC2C=C(CS(N)(=O)=O)C=CC=2)[N:30]=1.N1CCC[C@@H]1C(N)=O>>[S:24]([CH2:23][C:19]1[CH:18]=[C:17]([NH:16][C:12]2[N:13]=[CH:14][N:15]=[C:10]([N:5]3[CH2:6][CH2:7][CH2:8][C@@H:4]3[C:3]([NH2:30])=[O:2])[N:11]=2)[CH:22]=[CH:21][CH:20]=1)(=[O:25])(=[O:26])[NH2:27]Komponenten
4
Versuchsvorschrift
B23 was obtained as a white powder by following the procedure reported for B4 using A1 and (R)-proline amide; yield: 65 mg (19%). MS (ES) C15H19N7O3S requires: 377. found: 378 (M+H)+.
Aufarbeitung
- customB23 was obtained as a white powder
Quellen und Nachweise
- ORD-Eintrag
- ord-bd7988fcbf69419f80ce5bca8e415488
- Quelldatensatz
- uspto-grants-2016_01
- Patentnummer
- US09226929B2
Verknüpfte Notizen
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