4-Bromo-2-methylpyridine → (R)-3-(4-Bromo-phenyl)-1-(2-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one
Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:9][C:10](N(OC)C)=[O:11])=[CH:4][CH:3]=1.Br[C:24]1[CH:29]=[CH:28][N:27]=[C:26]([CH3:30])[CH:25]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C@H:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=2[CH3:22])[CH2:9][C:10]([C:24]2[CH:29]=[CH:28][N:27]=[C:26]([CH3:30])[CH:25]=2)=[O:11])=[CH:6][CH:7]=1Komponenten
3
Versuchsvorschrift
In analogy to example 74, step 5, from (R)-3-(4-bromo-phenyl)-N-methoxy-N-methyl-3-o-tolyl-propionamide and 4-bromo-2-methylpyridine was prepared the title compound as yellow solid, MS (ESI+): m/z=394.0797 ([M+H]+, 1Br).
Quellen und Nachweise
- ORD-Eintrag
- ord-d27f3dbc6d1145f8a3dbe24ab85cea1d
- Quelldatensatz
- uspto-grants-2014_07
- Patentnummer
- US08765730B2
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