反応式
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]=[C:10]=[O:11])=[CH:5][CH:4]=1)#[N:2].[C:12]1([NH2:19])[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH2:18].Br[CH:21]([C:23]1[CH:31]=[CH:30][C:26]([C:27]([OH:29])=[O:28])=[CH:25][CH:24]=1)[CH3:22].C(=O)([O-])[O-].[K+].[K+]>C(OCC)C.CN(C=O)C>[C:27]([C:26]1[CH:30]=[CH:31][C:23]([CH:21]([NH:18][C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[NH:19][C:10](=[O:11])[NH:9][C:6]2[CH:5]=[CH:4][C:3]([C:1]#[N:2])=[CH:8][CH:7]=2)[CH3:22])=[CH:24][CH:25]=1)([OH:29])=[O:28]参加物
7
実験手順
12.8 g (88.8 mmol) 4-cyanophenylisocyanat were dissolved in 500 ml diethyl ether at rt. 9.6 g (88.8 mmol) o-phenylene diamine were added with stirring. After stirring overnight, the reaction mixture was filtrated and the solid washed with diethylether. The so prepared mono-urea derivative was sufficient pure for further reactions. 3.78 (15 mmol) were dissolved in 30 ml anhydrous dry DMF, 3.44 g (15 mmol) 4-(1-bromoethyl)-benzoic acid and 2 g potassium carbonate were added and stirred for 3 days at rt. The solvent was removed under reduced pressure, the product dissolved in ethyl acetate and extracted with 1 m HCl, water and brine. The organic phase was dried over sodium sulfate and the solvent removed under reduced pressure.
後処理
- stirringAfter stirring overnight
- filtrationthe reaction mixture was filtrated
- washthe solid washed with diethylether
- customThe so prepared mono-urea derivative
- stirringstirred for 3 days at rt
- customThe solvent was removed under reduced pressure
- dissolutionthe product dissolved in ethyl acetate
- extractionextracted with 1 m HCl, water and brine
- dry with materialThe organic phase was dried over sodium sulfate
- customthe solvent removed under reduced pressure
出典と根拠
- ORDレコード
- ord-5171a0f3ec00423cbedc952e18e7cb9a
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06706715B2
関連ノート
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