反応式
[C:1]([NH2:9])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([O-])([O-])=O.[K+].[K+].[C@@H]1(N)CCCC[C@H]1N.Cl[C:25]1[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=1>[Cu]I>[CH3:31][C:28]1[CH:29]=[CH:30][C:25]([NH:9][C:1](=[O:8])[C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:26][CH:27]=1参加物
反応条件
- 温度
- 140 °C
実験手順
An oven-dried resealable Schlenk tube was charged with CuI (20 mg, 0.105 mmol, 5.1 mol %), benzamide (250 mg, 2.06 mmol), K2CO3 (600 mg, 4.34 mmol), evacuated and backfilled with argon. trans-1,2-Cyclohexanediamine (26 μL, 0.217 mmol, 10.5 mol %) and 4-chlorotoluene (1.0 mL, 8.44 mmol) were added under argon. The Schlenk tube was sealed and the reaction mixture was stirred magnetically at 140° C. for 46 h. The resulting black suspension was cooled to room temperature and filtered through a 0.5×1 cm pad of silica gel eluting with 10 mL of ethyl acetate. The filtrate was concentrated and the residue was purified by flash chromatography on silica gel (2×20 cm; hexane-ethyl acetate 2:1; 15 mL fractions). Fractions 5-15 were concentrated, the solid residue was suspended in 10 mL of hexane and filtered to provide 413 mg (95% yield) of the product as white crystals. The 1H NMR spectrum was in accord with that reported by Erdik et al. Erdik, E.; Daskapan, T. J. Chem. Soc., Perkin Trans. 1 1999, 3139.
後処理
- customevacuated
- customThe Schlenk tube was sealed
- temperatureThe resulting black suspension was cooled to room temperature
- filtrationfiltered through a 0.5×1 cm pad of silica gel eluting with 10 mL of ethyl acetate
- concentrationThe filtrate was concentrated
- customthe residue was purified by flash chromatography on silica gel (2×20 cm; hexane-ethyl acetate 2:1; 15 mL fractions)
- concentrationFractions 5-15 were concentrated
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-385b4fa845984ec193bb130172928355
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06867298B2
関連ノート
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