反応式
[CH3:1][N:2]1[C:10]2[N:9]=[CH:8][NH:7][C:6]=2[C:5](=[O:11])[NH:4][C:3]1=[O:12].C(=O)([O-])[O-].[K+].[K+].[Cl:19][C:20]1[CH:35]=[CH:34][C:23]([C:24]([C:26]2[CH:33]=[CH:32][C:29]([CH2:30]Br)=[CH:28][CH:27]=2)=[O:25])=[CH:22][CH:21]=1.O>CN(C=O)C.C(OCC)(=O)C>[Cl:19][C:20]1[CH:21]=[CH:22][C:23]([C:24]([C:26]2[CH:33]=[CH:32][C:29]([CH2:30][N:7]3[C:6]4[C:5](=[O:11])[NH:4][C:3](=[O:12])[N:2]([CH3:1])[C:10]=4[N:9]=[CH:8]3)=[CH:28][CH:27]=2)=[O:25])=[CH:34][CH:35]=1参加物
7
実験手順
To a solution of 3-methylxanthine (1.06 g) in DMF (26 ml) were added potassium carbonate (1.06 g) and 4-(4-chlorobenzoyl)benzyl bromide (1.98 g) and the mixture was stirred at room temperature for 24 hours. To this reaction mixture were added water and ethyl acetate and the floating matter was filtered off and the filtrate aqueous solution was diluted with 1N-hydrochloric acid and extracted with chloroform. The extract was washed with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. The solvent was then distilled off and the residue was washed with ethyl acetate to provide the title compound as colorless powder (239 mg, 10%). 1H-NMR (CDC13) 8: 3.54(3H,s), 3.57(3H,s), 7.41-7.52(4H,m), 7.68-7.81(5H,m).
後処理
- filtrationthe floating matter was filtered off
- additionthe filtrate aqueous solution was diluted with 1N-hydrochloric acid
- extractionextracted with chloroform
- washThe extract was washed with saturated aqueous NaCl solution
- dry with materialdried over anhydrous sodium sulfate
- distillationThe solvent was then distilled off
- washthe residue was washed with ethyl acetate
出典と根拠
- ORDレコード
- ord-263f4060c9a346398982594f4c89d517
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05753664
関連ノート
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