関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 1,10-Phenanthroline | HCID 1318 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 3-Iodobenzonitrile | HCID 144341 | — |
| 反応物 | trans-Dibenzylideneacetone | HCID 5354370 | — |
| 反応物 | HCID 178420123 | HCID 178420123 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrile | HCID 11242036 | 8.3% |
反応手順
To a flame dried, argon purged screw-cap vial, containing copper (I) triflate.benzene complex (0.01 g, 0.03 mmol), 1,10-phenanthroline (0.10 g, 0.54 mmol), trans-dibenzylideneacetone (0.01 g, 0.03 mmol) and cesium carbonate (0.20g, 0.60 mmol) was added a solution of 4-(2-pyridyl)imidazole (0.08 g, 0.54 mmol) and 3-iodobenzonitrile (0.19 g, 0.82 mmol) in ortho-xylene (2 mL). The resulting brownish black reaction mixture was heated overnight at 120° C. After cooling, the reaction mixture was diluted with dichloromethane (20 mL) and washed sequentially with saturated ammonium chloride (20 mL) and brine (20 mL). The organic phase was then dried with sodium sulfate, filtered, and concentrated in vacuo. Silica gel chromatography of the crude residue using 1% methanol (2 M in ammonia) in dichloromethane afforded 11 mg of 4-(2-pyridyl)-1-(3-cyanophenyl)-1H-imidazole, as an off-white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06660753B2 |
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| 出典データセット | uspto-grants-2003_12 |
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| ORD ID | ord-16b5d23edf5a421c90fe9c73a295dcbc |
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| 出典メモ | uspto-grants-2003_12 |
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