반응식
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].C(O[CH:14](OCC)[N:15]([CH3:17])[CH3:16])C>>[CH3:14][N:15](/[CH:17]=[CH:1]/[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9])[CH3:16]참가 물질
3
실험 절차
Commercially available 4-methyl-3-nitropyridine is condensed with N,N-dimethylformamide diethyl acetal to provide E-4-[2-(N,N-dimethylamino)-1-ethenyl]-3-nitropyridine, which is then subjected to catalytic hydrogenation to give 6-azaindole.
출처 및 근거
- ORD 기록
- ord-e0d7c6e2ad1f47c78b58f92fa658c027
- 출처 데이터셋
- uspto-grants-1995_11
- 특허 번호
- US05468757
연결된 노트
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