Hexane → 5-Carbomethoxy-2-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]propyl]-1,2,4-triazole
反応式
CCCCCC.[H-].[Na+].[C:9]([C:13]1[NH:17][N:16]=[CH:15][N:14]=1)([O:11][CH3:12])=[O:10].[CH3:18][N:19]1[N:23]=[N:22][C:21]([C:24]2[CH:34]=[C:33]([CH3:35])[C:27]([O:28][CH2:29][CH2:30][CH2:31]Br)=[C:26]([CH3:36])[CH:25]=2)=[N:20]1>CN(C=O)C>[C:9]([C:13]1[N:14]=[CH:15][N:16]([CH2:31][CH2:30][CH2:29][O:28][C:27]2[C:26]([CH3:36])=[CH:25][C:24]([C:21]3[N:22]=[N:23][N:19]([CH3:18])[N:20]=3)=[CH:34][C:33]=2[CH3:35])[N:17]=1)([O:11][CH3:12])=[O:10]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
Hexane washed 60% NaH (22 mg, 0.55 mmol) in 0.5 ml of DMF was added at 20° C. to a solution of 5-carbomethoxy-1,2,4-triazole (63.5 mg, 0.5 mmol) in 0.5 ml of DMF and the mixture was stirred for 1 h. To the above mixture was added at 20° C. 3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propylbromide (163 mg, 0.5 mmol) in 0.5 ml of DMF and the mixture was stirred at 20° C. for 18 h. The mixture was partitioned between ice/water and ethyl acetate. The aqueous layer was extracted with ethyl acetate (3×), and the organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by silica column chromatography (20 cm column, ethyl acetate/hexane, 1/5 - 1/0; methylene chloride/acetone) to afford 74 mg (40%) of 5-carbomethoxy-2-[3-[4-(2-methyl-tetrazol-5-yl)-2,6-dimethylphenoxy]-propyl]-1,2,4-triazole.
後処理
- additionTo the above mixture was added at 20° C
- customThe mixture was partitioned between ice/water and ethyl acetate
- extractionThe aqueous layer was extracted with ethyl acetate (3×)
- dry with materialthe organic layer was dried over sodium sulfate
- concentrationconcentrated in vacuo
- customThe residue was purified by silica column chromatography (20 cm column, ethyl acetate/hexane, 1/5 - 1/0; methylene chloride/acetone)
出典と根拠
- ORDレコード
- ord-3e7a4f0526ff434da9eaefe7c07148f9
- 出典データセット
- uspto-grants-1998_02
- 特許番号
- US05721261
反応ノート
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