Dimethylformamide → 6-chloro-5-(trifluoromethyl)-1H-indole
反応式
[Cl:1][C:2]1[C:3]([C:15]([F:18])([F:17])[F:16])=[CH:4][C:5]([C:9]#[C:10][Si](C)(C)C)=[C:6]([CH:8]=1)[NH2:7].CN(C)C=O>[Cu]I.C(OCC)C>[Cl:1][C:2]1[CH:8]=[C:6]2[C:5]([CH:9]=[CH:10][NH:7]2)=[CH:4][C:3]=1[C:15]([F:18])([F:17])[F:16]参加物
実験手順
A mixture of 5-chloro-4-(trifluoromethyl)-2-[(trimethylsilyl)ethynyl]aniline (16.5 g), copper(I) iodide (20.4 g) and dimethylformamide (100 ml) was stirred at room temperature for 10 min and then stirred with heating at 100° C. for 2.5 hr. The reaction mixture was allowed to cool, diethyl ether was added and the mixture was stirred at room temperature. The reaction mixture was filtered through a celite (trademark) filter, and the filtrate was washed with water and saturated brine, dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give a brown oil. The oil was purified by silica gel column chromatography (elution solvent:ethyl acetate-hexane (1:5-1:3)) to give 6-chloro-5-(trifluoromethyl)-1H-indole (5.75 g, yield 46%).
後処理
- stirringstirred
- temperaturewith heating at 100° C. for 2.5 hr
- temperatureto cool
- stirringthe mixture was stirred at room temperature
- filtrationThe reaction mixture was filtered through a celite (trademark)
- filtrationfilter
- washthe filtrate was washed with water and saturated brine
- dry with materialdried over anhydrous sodium sulfate
- customThe solvent was evaporated under reduced pressure
- customto give a brown oil
- customThe oil was purified by silica gel column chromatography (elution solvent:ethyl acetate-hexane (1:5-1:3))
出典と根拠
- ORDレコード
- ord-2dbd9636e5ca4c3aa8ca4ca2bf838207
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07994196B2
反応ノート
読み込み中…