Reaktionsgleichung
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]([N:11]2[CH2:16][CH2:15][C@:14]([CH2:23][C:24]([OH:27])([CH3:26])[CH3:25])([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[O:13][C:12]2=[O:28])[CH3:10])=[CH:5][CH:4]=1)#[CH:2].Br[C:30]1[CH:31]=[CH:32][C:33](=[O:37])[N:34]([CH3:36])[CH:35]=1>>[OH:27][C:24]([CH3:25])([CH3:26])[CH2:23][C@@:14]1([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[O:13][C:12](=[O:28])[N:11]([C@H:9]([C:6]2[CH:5]=[CH:4][C:3]([C:1]#[C:2][C:30]3[CH:31]=[CH:32][C:33](=[O:37])[N:34]([CH3:36])[CH:35]=3)=[CH:8][CH:7]=2)[CH3:10])[CH2:16][CH2:15]1Komponenten
3
Versuchsvorschrift
The title compound was prepared from 3-[(S)-1-(4-ethynyl-phenyl)-ethyl]-(S)-6-(2-hydroxy-2-methyl-propyl)-6-phenyl-[1,3]oxazinan-2-one and 5-bromo-1-methyl-1H-pyridin-2-one following a procedure analogous to that described in Example 31. LC-MS (Method 1): tR=3.46 min; Mass spectrum (ESI+): m/z=485 [M+H]+.
Quellen und Nachweise
- ORD-Eintrag
- ord-0c1c1371354c430088cccb6945bfbdff
- Quelldatensatz
- uspto-grants-2014_11
- Patentnummer
- US08883778B2
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