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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80105생성일: 2026년 10월 25일

Potassium Carbonate → 1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/80105

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물3-Bromo-5-(trifluoromethyl)pyridineHCID 11127991—
반응물1-Naphthalen-2-yl-imidazolidin-2-oneHCID 59636167—
촉매Copper iodideHCID 83717—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
생성물1-Naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 5963621652%

반응 조건

온도110 °C

반응 단계

Copper iodide (12.6 mg, 0.066 mmol), trans-1,2-diamino cyclohexane (22.79 mg, 0.199 mmol) and potassium carbonate (183.5 mg, 1.32 mmol) were added to 1,4-dioxane (5 mL) and 3-bromo-5-trifluoromethyl-pyridine (150 mg, 0.66 mmol) previously degassed with argon (10 minutes). The reaction was purged with argon for a further 10 minutes, followed by the addition of 1-naphthalen-2-yl-imidazolidin-2-one (I-79b: 140 mg, 0.66 mmol) and the resulting mixture was heated to reflux at 110° C. for 15 hours. The reaction was monitored by TLC (50% ethyl acetate in hexane). The reaction mixture was filtered through celite and the bed was washed with chloroform. The organic layer was dried over Na2O4 and concentrated. Purification by column chromatography (using silica gel of mesh size of 60-120, 30% EtOAc in hexane as eluant) afforded 120 mg (52% yield) of 1-naphthalen-2-yl-3-(5-trifluoromethyl-pyridin-3-yl)-imidazolidin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-b4701bd379cf4461a06ebbf58e991c9b
출처 메모uspto-grants-2014_09