Reaktionsgleichung
[CH3:1][S:2]([C:5]1[S:9][C:8]([CH2:10][NH:11][C:12]([C:14]2[C:19](=[O:20])[C:18](Br)=[C:17]([CH3:22])[N:16]([CH:23]([CH3:25])[CH3:24])[CH:15]=2)=[O:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[F:26][CH:27]([F:37])[C:28]1[CH:29]=[C:30](B(O)O)[CH:31]=[CH:32][CH:33]=1>>[CH3:1][S:2]([C:5]1[S:9][C:8]([CH2:10][NH:11][C:12]([C:14]2[C:19](=[O:20])[C:18]([C:32]3[CH:31]=[CH:30][CH:29]=[C:28]([CH:27]([F:37])[F:26])[CH:33]=3)=[C:17]([CH3:22])[N:16]([CH:23]([CH3:25])[CH3:24])[CH:15]=2)=[O:13])=[CH:7][CH:6]=1)(=[O:4])=[O:3]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
Example 40 is prepared following the procedure for Example 24.1, substituting preparation 24 with preparation 39a and replacing 3-(trifluoromethyl)phenylboronic acid with 3-(difluoromethyl)phenylboronic acid. ESI mass spectrum: [M+H]+=495; Retention time HPLC: 0.82 min (Z011_S03).
Aufarbeitung
- customExample 40 is prepared
- custompreparation 24
Quellen und Nachweise
- ORD-Eintrag
- ord-d807105bbafc409190552bf0eb805327
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09340507B2
Verknüpfte Notizen
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