HCID 58109551, compound → HCID 59635662, compound
Reaction equation
[CH3:1][O:2][CH2:3][C@@:4]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[O:9][C:8](=[O:10])[N:7]([C@H:11]([C:13]2[CH:18]=[CH:17][C:16](B3OC(C)(C)C(C)(C)O3)=[CH:15][CH:14]=2)[CH3:12])[CH2:6][CH2:5]1.[CH3:34][N:35]1[CH:40]=[CH:39][C:38](OS(C(F)(F)F)(=O)=O)=[CH:37][C:36]1=[O:49]>>[CH3:1][O:2][CH2:3][C@@:4]1([C:28]2[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=2)[O:9][C:8](=[O:10])[N:7]([C@H:11]([C:13]2[CH:14]=[CH:15][C:16]([C:38]3[CH:39]=[CH:40][N:35]([CH3:34])[C:36](=[O:49])[CH:37]=3)=[CH:17][CH:18]=2)[CH3:12])[CH2:6][CH2:5]1Participants
3
Procedure
The title compound was prepared from (R)-6-(methoxymethyl)-6-phenyl-3-((S)-1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)-1,3-oxazinan-2-one and trifluoro-methanesulfonic acid 1-methyl-2-oxo-1,2-dihydro-pyridin-4-yl ester following a procedure analogous to that described in Example 76. Mass spectrum (ESI+): m/z=433 [M+H]+.
Sources & evidence
- ORD record
- ord-13540cb1f34f4dd6ac29f8be1604665f
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08754076B2
Reaction notes
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