Iodoethane → 3-Bromo-5-(methoxymethyl)pyridine
반응식
[CH3:1][O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([Br:10])[CH:7]=[N:6][CH:5]=1.ICC>>[Br:10][C:8]1[CH:7]=[N:6][CH:5]=[C:4]([CH2:3][O:2][CH3:1])[CH:9]=1참가 물질
3
실험 절차
Prepared in a similar manner to Example 26a starting from (5-bromopyridin-3-yl)methanol (example 26d) and iodoethane. Yield: 89%. 1H NMR (400 MHz, CDCl3): δ 3.43 (s, 3H), 4.46 (s, 2H), 7.85 (s, 1H), 8.47 (s, 1H), 8.61 (s, 1H).
후처리
- customPrepared in a similar manner to Example 26a
출처 및 근거
- ORD 기록
- ord-154659c0d825404ba641e6ff01cac9ab
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07842324B2
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