6-Chloro-2-methyl-3-nitropyridine → 6-(3,3-Difluoropiperidin-1-yl)-2-methyl-3-nitropyridine
반응식
Cl[C:2]1[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=1.[F:12][C:13]1([F:19])[CH2:18][CH2:17][CH2:16][NH:15][CH2:14]1>>[F:12][C:13]1([F:19])[CH2:18][CH2:17][CH2:16][N:15]([C:2]2[N:7]=[C:6]([CH3:8])[C:5]([N+:9]([O-:11])=[O:10])=[CH:4][CH:3]=2)[CH2:14]1참가 물질
3
실험 절차
Prepared from 6-chloro-2-methyl-3-nitropyridine and 3,3-difluoropiperidine following the method used to prepare Intermediate 51. LCMS (ES+) 258.05 (M+H)+, RT 3.069 minutes (method 1).
후처리
- customLCMS (ES+) 258.05 (M+H)+, RT 3.069 minutes (method 1)
출처 및 근거
- ORD 기록
- ord-52621314b25d48c0a6f4b0e5f8cf76df
- 출처 데이터셋
- uspto-grants-2015_08
- 특허 번호
- US09096614B2
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