2-Chloro-5-nitropyridine → Tert-butyl 1-(5-aminopyridin-2-yl)pyrrolidin-3-ylcarbamate
반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-])=O)=[CH:4][N:3]=1.[NH:11]1[CH2:15][CH2:14][C@@H:13]([NH:16][C:17](=[O:23])[O:18][C:19]([CH3:22])([CH3:21])[CH3:20])[CH2:12]1>>[NH2:8][C:5]1[CH:6]=[CH:7][C:2]([N:11]2[CH2:15][CH2:14][CH:13]([NH:16][C:17](=[O:23])[O:18][C:19]([CH3:21])([CH3:20])[CH3:22])[CH2:12]2)=[N:3][CH:4]=1참가 물질
3
실험 절차
2-Chloro-5-nitropyridine was treated with tert-butyl (R)-(+)-pyrrolidin-3-ylcarbamate and subsequently hydrogenated by method C-c. This resulted in the product with the molecular weight of 278.36 (C14H22N4O2); MS (ESI): 279 (M+H+).
후처리
- customThis resulted in the product with the molecular weight of 278.36 (C14H22N4O2)
출처 및 근거
- ORD 기록
- ord-ca905e908a3b42a4b0ad7e779f63673c
- 출처 데이터셋
- uspto-grants-2007_05
- 특허 번호
- US07223788B2
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