Methylamine → Methyl(3-(5-methoxy-3-pyridyloxy)propyl)amine
반응식
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:7]=[C:8]([O:12][CH3:13])[CH:9]=[N:10][CH:11]=1.[CH3:14][NH2:15]>CO>[CH3:14][NH:15][CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[N:10][CH:9]=[C:8]([O:12][CH3:13])[CH:7]=1참가 물질
반응 조건
- 온도
- 100 °C
실험 절차
Crude 5-(3-chloropropoxy)-3-methoxypyridine (0.75 g, 3.73 mmol) was dissolved in methanol (10.5 mL) and added to a 40 wt % aqueous solution of methylamine (10.6 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 4 h. After cooling, the solution was concentrated by rotary evaporation. Saturated NaCl solution (50 mL) was added, and the mixture was basified with 10% NaOH solution to pH 11. The mixture was extracted with ether (4×50 mL). The combined ether extracts were dried (MgSO4), filtered and concentrated by rotary evaporation to give 0.54 g of a brown oil. The product was purified by column chromatography on silica gel (18 g) eluting with CHCl3—CH3OH (1:1, v/v) to remove impurities, followed by CHCl3—CH3OH-Et3N (50:50:2, v/v/v) to collect the product. Selected fractions containing the product were combined and concentrated by rotary evaporation. The resulting brown oil was dissolved in CHCl3 (25 mL), dried (MgSO4), filtered, and concentrated by rotary evaporation to give 0.228 g (31.2%) of a brown oil.
후처리
- customThe tube was sealed
- temperatureAfter cooling
- concentrationthe solution was concentrated by rotary evaporation
- additionSaturated NaCl solution (50 mL) was added
- extractionThe mixture was extracted with ether (4×50 mL)
- dry with materialThe combined ether extracts were dried (MgSO4)
- filtrationfiltered
- concentrationconcentrated by rotary evaporation
출처 및 근거
- ORD 기록
- ord-73845735b8a2412a9f7133d3c9cadc00
- 출처 데이터셋
- uspto-grants-2003_09
- 특허 번호
- US06627648B1
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