反応式
Cl[C:2]1C=CC(C#N)=CN=1.[NH2:10][C:11]1[N:16]=[C:15]([NH:17][CH2:18][CH2:19][NH:20][C:21]2[CH:26]=[CH:25][C:24]([C:27]3[NH:28][CH:29]=[CH:30][N:31]=3)=[C:23]([C:32]3[CH:37]=[CH:36][C:35]([Cl:38])=[CH:34][C:33]=3[Cl:39])[N:22]=2)[CH:14]=[CH:13][C:12]=1[N+]([O-])=O>>[Cl:39][C:33]1[CH:34]=[C:35]([Cl:38])[CH:36]=[CH:37][C:32]=1[C:23]1[N:22]=[C:21]([NH:20][CH2:19][CH2:18][NH:17][C:15]2[N:16]=[CH:2][C:12]([C:11]#[N:10])=[CH:13][CH:14]=2)[CH:26]=[CH:25][C:24]=1[C:27]1[NH:31][CH:30]=[CH:29][N:28]=1参加物
3
実験手順
6-[(2-{[6-(2,4-dichlorophenyl)-5-imidazolyl-2-pyridyl]amino}ethyl)amino]-pyridine-3-carbonitrile was prepared from 2-chloropyridine-5-carbonitrile using the general method for {2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}[6-(2,4-dichlorophenyl)-5-imidazolyl(2-pyridyl)]amine.
出典と根拠
- ORDレコード
- ord-3d7d2becd2254413bf48ef997796fe2d
- 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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