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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80039생성일: 2026년 10월 24일

2-Bromonaphthalene → 1-(4-Methyl-pyridin-3-yl)-3-naphthalen-2-yl-imidazolidin-2-one

https://huagongshe.com/ko/reaction/80039

반응식

참여 물질

역할이름HCID투입량
반응물2-BromonaphthaleneHCID 11372—
반응물Potassium CarbonateHCID 11430—
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물1-(4-Methylpyridin-3-yl)imidazolidin-2-oneHCID 59636170—
촉매Copper iodideHCID 83717—
용매MethanolHCID 887—
용매ChloroformHCID 6212—
용매1,4-DioxaneHCID 31275—
생성물1-(4-Methyl-pyridin-3-yl)-3-naphthalen-2-yl-imidazolidin-2-oneHCID 4987186673%

반응 조건

온도110 °C

반응 단계

Copper iodide (21.5 mg, 0.113 mmol), trans-1,2-diamino cyclohexane (0.041 mL, 0.339 mmol) and potassium carbonate (313 mg, 2.26 mmol) were added to 1,4-Dioxane (15 mL) previously sparged with argon (10 minutes). The reaction mixture was sparged with argon for a further 10 minutes, followed by the addition of 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 200 mg, 1.13 mmol) and 2-bromo naphthalene (234 mg, 1.13 mmol). The resulting mixture was heated to reflux at 110° C. for 15 hours. The reaction was monitored by TLC (10% MeOH in chloroform). The reaction mixture was filtered through a celite and the bed was washed with chloroform. The organic layer was dried over Na2SO4 and concentrated. Purification by column chromatography (using silica gel of mesh size of 60-120, 1% MeOH in chloroform as eluent) afforded 250 mg (73% yield) of 1-(4-methyl-pyridin-3-yl)-3-naphthalen-2-yl-imidazolidin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-4c37a5aae42d4d56a69f1a90baaabf45
출처 메모uspto-grants-2014_09