反応式
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:16])=[C:6]([C:8]2[CH:13]=[C:12](Cl)[N:11]=[C:10]([NH2:15])[N:9]=2)[CH:7]=1.[Br:17][C:18]1[CH:23]=[CH:22][C:21]([NH2:24])=[CH:20][CH:19]=1>>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH3:16])=[C:6]([C:8]2[N:9]=[C:10]([NH2:15])[N:11]=[C:12]([NH:24][C:21]3[CH:22]=[CH:23][C:18]([Br:17])=[CH:19][CH:20]=3)[CH:13]=2)[CH:7]=1参加物
3
実験手順
Following the method described in Example 26, 4-(5-bromo-2-methyl-phenyl)-6-chloro-pyrimidin-2-ylamine and 4-bromo-phenylamine provided the title compound (91% yield). 1H NMR (DMSO-d6) δ 2.34 (s, 3H, CH3), 6.37 (s, 1H, Ar), 7.40 (d, 1H, J=8.9 Hz, Ar), 7.59 (d, 2H, J=8.7 Hz, Ar), 7.70-7.71 (m, 2H, Ar), 7.82-7.84 (m, 2H, Ar), 10.89 (br s, 1H, NH).
出典と根拠
- ORDレコード
- ord-ebc24cc6a85a45a39f40bed4fa88c9c3
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07419984B2
関連ノート
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