반응식
[NH2:1][C:2]1[C:7]([N+:8]([O-])=O)=[CH:6][CH:5]=[C:4]([CH3:11])[N:3]=1>CO.[Pd]>[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[C:4]([CH3:11])[N:3]=1참가 물질
4
실험 절차
2-Amino-6-methyl-3-nitropyridine (754 mg, 4.92 mmol) was suspended in MeOH, and 10% Pd/C was added. The mixture was stirred briskly at RT under H2 (balloon). After 4 h, the reaction was filtered through Celite®, and the filtrate was concentrated under vacuum to afford the title compound (677 mg, quantitative): 1H NMR (250 MHz, CD3OD) δ 6.82 (d, 1H), 6.36 (d, 1H), 2.25 (s, 3H).
후처리
- filtrationthe reaction was filtered through Celite®
- concentrationthe filtrate was concentrated under vacuum
출처 및 근거
- ORD 기록
- ord-ad8f0c7299894dfb99ddfd3081cba88d
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05977101
연결된 노트
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