Reaktionsgleichung
[C:1]([O:5][C:6](=[O:22])[NH:7][CH:8]([C:15]1[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][CH:16]=1)[C:9](=[O:14])N(OC)C)([CH3:4])([CH3:3])[CH3:2].Br[C:24]1[CH:29]=[CH:28][C:27]([O:30][CH:31]([CH3:36])[C:32]([F:35])([F:34])[F:33])=[CH:26][CH:25]=1>>[C:1]([O:5][C:6](=[O:22])[NH:7][CH:8]([C:15]1[CH:16]=[CH:17][C:18]([Cl:21])=[CH:19][CH:20]=1)[C:9](=[O:14])[C:24]1[CH:25]=[CH:26][C:27]([O:30][CH:31]([CH3:36])[C:32]([F:33])([F:34])[F:35])=[CH:28][CH:29]=1)([CH3:2])([CH3:3])[CH3:4]Komponenten
3
Edukt 2
Produkt 1
Versuchsvorschrift
The title compound was prepared from rac-[(4-chloro-phenyl)-(methoxy-methyl-carbamoyl)-methyl]-carbamic acid tert-butyl ester (Intermediate 8) and rac-1-bromo-4-(2,2,2-trifluoro-1-methyl-ethoxy)-benzene (Intermediate 35) in analogy to Example 1a): MS (ISP): 458.2 (M+H)+.
Quellen und Nachweise
- ORD-Eintrag
- ord-a339dd7dc2b946d989b6a0154580aafc
- Quelldatensatz
- uspto-grants-2013_02
- Patentnummer
- US08367838B2
Verknüpfte Notizen
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