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HRID 432003作成日:2026年10月23日

1,10-Phenanthroline → 3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrile

https://huagongshe.com/ja/reaction/432003

反応式

関与物質

役割名称HCID仕込み量
反応物1,10-PhenanthrolineHCID 1318—
反応物Cesium carbonateHCID 10796—
反応物3-IodobenzonitrileHCID 144341—
反応物trans-DibenzylideneacetoneHCID 5354370—
反応物HCID 178420123HCID 178420123—
溶媒DichloromethaneHCID 6344—
溶媒O-XyleneHCID 7237—
生成物3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrileHCID 112420368.3%

反応条件

温度120 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06660753B2
出典データセットuspto-grants-2003_12
ORD IDord-16b5d23edf5a421c90fe9c73a295dcbc
出典メモuspto-grants-2003_12