Water → (3R*,4R*)-4-(3-Bromo-phenyl)-3-hydroxy-piperidine-1-carboxylic acid t-butyl ester
반응식
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH:12]=[C:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([Br:20])[CH:15]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].CC#N.[OH2:24]>>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][C@H:11]([C:14]2[CH:19]=[CH:18][CH:17]=[C:16]([Br:20])[CH:15]=2)[C@@H:12]([OH:24])[CH2:13]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]참가 물질
4
실험 절차
The title compound is prepared analogously as described for the title B compound in Example 1 from the title A compound, 4-(3-bromo-phenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid t-butyl ester: MS 356.2/358.1 [M+H]+; retention time 6.59 min (HPLC, Nucleosil C18; 5→100% CH3CN in H2O within 8 min).
출처 및 근거
- ORD 기록
- ord-bb2c46cd49334552b63c33ea5636b856
- 출처 데이터셋
- uspto-grants-2010_07
- 특허 번호
- US07754727B2
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