Water → 3-Ethyl-5-methyl-2-naphthalen-1-yl-3h-imidazole-4-carboxylic acid ethyl ester
反応式
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=2)=[N:9][C:10]=1[CH3:11])=[O:5])[CH3:2].[H-].[Na+].[CH2:24](I)[CH3:25].O>CN(C=O)C>[CH2:1]([O:3][C:4]([C:6]1[N:7]([CH2:24][CH3:25])[C:8]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=2)=[N:9][C:10]=1[CH3:11])=[O:5])[CH3:2].[CH2:1]([O:3][C:4]([C:6]1[N:7]=[C:8]([C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=2)[N:9]([CH2:24][CH3:25])[C:10]=1[CH3:11])=[O:5])[CH3:2]参加物
7
反応物 4
生成物 2
試薬・触媒・溶媒 1
反応条件
- 温度
- 0 °C
実験手順
To a solution of 5-methyl-2-naphthalen-1-yl-3H-imidazole-4-carboxylic acid ethyl ester (1.5 g) in DMF (30 ml) is added NaH (320 mg, 60%) at rt. The solution is stirred for 30 min, and EtI (0.6 ml) is added. After 30 min, the mixture is cooled to 0° C. and H2O is added. The mixture is then extracted with EtOAc. The extracts are combined, dried, evaporated and purified by column (EtOAc:Hexanes 1:1) to give 3-ethyl-5-methyl-2-naphthalen-1-yl-3H-imidazole-4-carboxylic acid ethyl ester [LCMS 309.4 (M+1); δ 4.10 ppm (CH2CH3)] and its regioisomer 1-ethyl-5-methyl-2-naphthalen-1-yl-1H-imidazole-4-carboxylic acid ethyl ester [LCMS 309.4 (M+1); δ 3.72 ppm (CH2CH3)].
後処理
- waitAfter 30 min
- extractionThe mixture is then extracted with EtOAc
- customdried
- customevaporated
- custompurified by column (EtOAc:Hexanes 1:1)
出典と根拠
- ORDレコード
- ord-6865d417dc3a4acbabe299198449a15e
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07728009B1
反応ノート
読み込み中…