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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2216893생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/2216893

반응식

참여 물질

역할이름HCID투입량
반응물1,10-PhenanthrolineHCID 1318—
반응물Cesium carbonateHCID 10796—
반응물3-IodobenzonitrileHCID 144341—
반응물trans-DibenzylideneacetoneHCID 5354370—
반응물HCID 178420123HCID 178420123—
용매DichloromethaneHCID 6344—
용매O-XyleneHCID 7237—
생성물3-(4-Pyridin-2-yl-imidazol-1-yl)-benzonitrileHCID 112420368.3%

반응 조건

온도120 °C

반응 단계

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 (0.20 g, 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07112595B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-899a4a96a3cf41e4a4fa6d93a65fb868
출처 메모uspto-grants-2006_09