反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7](Cl)=O)=[CH:5][CH:4]=1.ClC1C=C(Cl)C=CC=1C1[C:27]([C:28]2[NH:29][CH:30]=[CH:31][N:32]=2)=[CH:26][N:25]=[C:24]([NH:33][CH2:34][CH2:35][NH:36][C:37]2[CH:42]=[CH:41][C:40]([N+:43]([O-:45])=[O:44])=[CH:39][N:38]=2)[N:23]=1>>[NH:29]1[CH:30]=[CH:31][N:32]=[C:28]1[C:27]1[C:7]([C:6]2[CH:10]=[CH:11][C:3]([C:2]([F:13])([F:12])[F:1])=[CH:4][CH:5]=2)=[N:23][C:24]([NH:33][CH2:34][CH2:35][NH:36][C:37]2[CH:42]=[CH:41][C:40]([N+:43]([O-:45])=[O:44])=[CH:39][N:38]=2)=[N:25][CH:26]=1参加物
3
実験手順
{5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}{2-[(5-nitro(2-pyridyl))amino]ethyl}amine was prepared from 4-(trifluoromethyl)benzoyl chloride using the general method for [4-(2,4-dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]{2-[(5-nitro(2-pyridyl))amino]ethyl}amine.
出典と根拠
- ORDレコード
- ord-55cfa86ad7fb4feba4a343de3f4513b0
- 出典データセット
- uspto-grants-2002_12
- 特許番号
- US06489344B1
関連ノート
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