反応式
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.N1C=CC=CC=1[N:15]1[C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[N:17]=[C:16]1/[CH:24]=[CH:25]/[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.Cl>CO>[ClH:1].[CH3:8][C:7]1[C:2]([N:15]2[C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=3[N:17]=[C:16]2/[CH:24]=[CH:25]/[C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[N:3][CH:4]=[CH:5][CH:6]=1参加物
5
実験手順
Free base of the titled compound was prepared from 2-styryl-1-benzimidazole and 2-chloro-3-methylpyridine according to the preparation of (E)-1-(2-pyridyl)-2-styryl-1H-benzimidazole (Example 1, method B). The free base was treated with a 10% methanol solution of hydrogen chloride and concentrated to dryness. The residue was recrystallized from ethyl acetate/n-hexane to give the titled compound.
後処理
- concentrationconcentrated to dryness
- customThe residue was recrystallized from ethyl acetate/n-hexane
出典と根拠
- ORDレコード
- ord-c4cac8873b38476388b2519c8f40e940
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06310079B1
関連ノート
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