反応式
[CH3:1][C:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:17](Cl)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>CN(C)C=O>[CH2:17]([N:7]1[C:6]2[CH:5]=[CH:4][CH:3]=[C:2]([CH3:1])[C:10]=2[N:9]=[CH:8]1)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1参加物
実験手順
To a flask were added 1.0 g 4-methyl-1H-benzimidazole, 1.6 g potassium carbonate, 25 ml N,N-dimethylformamide and the mixture was stirred under nitrogen. 1.4 g Benzyl chloride were added and the mixture was heated to 60 C for 16 hours. Another 0.4 g of benzyl chloride were added and the reaction was heated to 70 C for 24 hours. The reaction was cooled to 50 C and quenched with 50 ml water and extracted with ethyl acetate. After washing with water, the solvent was removed and the product was purified by column chromatography using a gradient from 40% ethyl acetate in hexane to 75% ethyl acetate in hexane. Following removal of the solvent, the partially crystallized product was dissolved in 20 ml acetonitrile and treated with 0.1 g activated carbon. After refluxing for 20 minutes, the mixture was filtered through celite and the solvent was removed leaving a yellow oil which crystallized on standing, 1.0 g.
後処理
- temperaturethe mixture was heated to 60 C for 16 hours
- temperaturethe reaction was heated to 70 C for 24 hours
- temperatureThe reaction was cooled to 50 C
- customquenched with 50 ml water
- extractionextracted with ethyl acetate
- washAfter washing with water
- customthe solvent was removed
- customthe product was purified by column chromatography
- customremoval of the solvent
- dissolutionthe partially crystallized product was dissolved in 20 ml acetonitrile
- additiontreated with 0.1 g
- temperatureAfter refluxing for 20 minutes
- filtrationthe mixture was filtered through celite
- customthe solvent was removed
- customleaving a yellow oil which
- customcrystallized
出典と根拠
- ORDレコード
- ord-218b782235a04ad585e99327bd7560fa
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07538931B2
関連ノート
読み込み中…