反応式
[CH3:1][N:2]1[CH:6]=[CH:5][N:4]=[C:3]1[CH3:7].Cl[C:9]1[CH:14]=[CH:13][C:12]([C:15]#[N:16])=[CH:11][N:10]=1.[Cl:17][C:18]1[CH:23]=[C:22]([Cl:24])[CH:21]=[CH:20][C:19]=1[C:25]1C(C2NC=CN=2)=[CH:29][N:28]=[C:27]([NH:36][CH2:37][CH2:38][NH:39]C2C=CC([N+]([O-])=O)=CN=2)[N:26]=1>>[Cl:17][C:18]1[CH:23]=[C:22]([Cl:24])[CH:21]=[CH:20][C:19]=1[C:25]1[C:7]([C:3]2[N:2]([CH3:1])[CH:6]=[CH:5][N:4]=2)=[CH:29][N:28]=[C:27]([NH:36][CH2:37][CH2:38][NH:39][C:9]2[N:10]=[CH:11][C:12]([C:15]#[N:16])=[CH:13][CH:14]=2)[N:26]=1参加物
4
実験手順
6-[(2-{[4-(2,4-dichlorophenyl)-5-(1-methylimidazol-2-yl)pyrimidin-2-yl]amino}-ethyl)amino]pyridine-3-carbonitrile was prepared from 1,2-dimethylimidazole and 2-chloro-5-(cyano)pyridine 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-3108dd7de06347139d26d03e283095de
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07425557B2
関連ノート
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