反応式
[NH2:1][CH2:2][CH2:3][S:4][C:5]1[N:10]2[CH:11]=[CH:12][N:13]=[C:9]2[CH:8]=[CH:7][CH:6]=1.C(N(CC)CC)C.C([C:24]1([OH:33])[CH:32]=[CH:31][CH:30]=[CH:29][CH:25]1[C:26](Cl)=[O:27])(=O)C>C(Cl)Cl>[OH:33][C:24]1[CH:32]=[CH:31][CH:30]=[CH:29][C:25]=1[C:26]([NH:1][CH2:2][CH2:3][S:4][C:5]1[N:10]2[CH:11]=[CH:12][N:13]=[C:9]2[CH:8]=[CH:7][CH:6]=1)=[O:27]参加物
実験手順
To a solution of 5-[2-(amino)ethylthio]imidazo[1,2-a]pyridine (3.87 g, 20 mmoles) and triethylamine (5.58 ml, mmoles) in methylene chloride (200 ml) was added o-acetylsalicyloyl chloride (4.77 g, 24 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. After the solvent was distilled off, ethanol (60 ml) and 1N NaOH (40 ml) were added to the residue, followed by strirring for 1 hour. 1N HCl (40 ml) was added and ethanol was distilled off, and then the residue was extracted with chloroform and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1) to obtain 3.51 g of the desired product (56.0%, colorless solid).
後処理
- temperaturecooling
- stirringthe mixture was stirred at room temperature for 30 minutes
- distillationAfter the solvent was distilled off
- additionethanol (60 ml) and 1N NaOH (40 ml) were added to the residue
- addition1N HCl (40 ml) was added
- distillationethanol was distilled off
- extractionthe residue was extracted with chloroform
- dry with materialdried over anhydrous magnesium sulfate
- distillationAfter the solvent was distilled off
- customthe residue was purified by column chromatography (eluent: ethyl acetate/ethanol=10:1)
出典と根拠
- ORDレコード
- ord-eba409f04671494ab755179ec5ae31df
- 出典データセット
- uspto-grants-1995_03
- 特許番号
- US05395839
関連ノート
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