Triethylamine → N-[[2-(4-Methoxybenzyl)-2H-[1,2,4]triazol-3-yl]methyl]methylamine
반응식
[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:6]([CH2:7][N:8]2[C:12]([CH2:13]O)=[N:11][CH:10]=[N:9]2)=[CH:5][CH:4]=1.[CH2:17]([N:19](CC)CC)C.CS(Cl)(=O)=O>ClCCl>[CH3:1][O:2][C:3]1[CH:16]=[CH:15][C:6]([CH2:7][N:8]2[C:12]([CH2:13][NH:19][CH3:17])=[N:11][CH:10]=[N:9]2)=[CH:5][CH:4]=1참가 물질
실험 절차
[2-(4-Methoxybenzyl)-2H-[1,2,4]triazol-3-yl]methanol (0.50 g, 2.28 mmol) was dissolved in dichloromethane (10 ml), then triethylamine (0.36 ml, 2.60 mmol) was added. With cooling with ice, methanesulfonyl chloride (0.20 ml, 2.58 mmol) was added, followed by stirring at room temperature for 2 hours. The reaction liquid was concentrated, ethyl acetate was added, followed by washing. After drying over anhydrous sodium sulfate, the solvent was evaporated away under reduced pressure, and the resulting residue was dissolved in tetrahydrofuran (25 ml), then aqueous methylamine solution (40%, 5 ml) was added. After stirring at room temperature for 3 days, the reaction liquid was concentrated. This was diluted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain a pale yellow oil (0.44 g, 83%).
후처리
- additionwas added
- customThe reaction liquid
- concentrationwas concentrated
- additionethyl acetate was added
- washby washing
- dry with materialAfter drying over anhydrous sodium sulfate
- customthe solvent was evaporated away under reduced pressure
- dissolutionthe resulting residue was dissolved in tetrahydrofuran (25 ml)
- additionaqueous methylamine solution (40%, 5 ml) was added
- stirringAfter stirring at room temperature for 3 days
- customthe reaction liquid
- concentrationwas concentrated
- additionThis was diluted with ethyl acetate
- washwashed with water
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated away under reduced pressure
출처 및 근거
- ORD 기록
- ord-aef99694bce04a5ca74c422b290bbab7
- 출처 데이터셋
- uspto-grants-2010_06
- 특허 번호
- US07737166B2
반응 노트
불러오는 중…