1-[4-(2-Dimethylamino-ethylamino)-3-nitrophenyl]-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one → 1-[3-Amino-4-(2-dimethylaminoethylamino)phenyl]-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one
反応式
[CH3:1][N:2]([CH3:34])[CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][C:9]([N:12]2[CH:16]=[CH:15][N:14]([C:17]3[CH:22]=[CH:21][C:20]([O:23][C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)=[CH:19][CH:18]=3)[C:13]2=[O:30])=[CH:8][C:7]=1[N+:31]([O-])=O>ClCCl.C(O)(=O)C.[Zn]>[NH2:31][C:7]1[CH:8]=[C:9]([N:12]2[CH:16]=[CH:15][N:14]([C:17]3[CH:22]=[CH:21][C:20]([O:23][C:24]4[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=4)=[CH:19][CH:18]=3)[C:13]2=[O:30])[CH:10]=[CH:11][C:6]=1[NH:5][CH2:4][CH2:3][N:2]([CH3:34])[CH3:1]参加物
5
実験手順
Zinc dust (250 mg) was added to a solution of 1-[4-(2-dimethylamino-ethylamino)-3-nitrophenyl]-3-(4-phenoxyphenyl)-1,3-dihydroimidazol-2-one (50 mg) in dichloromethane (10 ml) and glacial acetic acid (1 ml). After 10 minutes, solids were removed by filtration and the filtrate was washed with saturated sodium carbonate solution. The organic phase was dried over magnesium sulfate and concentrated. The product with the molecular weight of 429.53 (C25H27N5O2); MS (ESI): 430 ([M+H]+), was obtained in this way.
後処理
- customsolids were removed by filtration
- washthe filtrate was washed with saturated sodium carbonate solution
- dry with materialThe organic phase was dried over magnesium sulfate
- concentrationconcentrated
- customMS (ESI): 430 ([M+H]+), was obtained in this way
出典と根拠
- ORDレコード
- ord-adca3358e96b49a3acfa98a756ae33aa
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141561B2
反応ノート
読み込み中…