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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80035생성일: 2026년 10월 23일

Potassium Carbonate → 1-(1-Oxo-indan-5-yl)-3-pyridin-3-yl-imidazolidin-2-one

https://huagongshe.com/ko/reaction/80035

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물5-Bromo-1-indanoneHCID 520695—
반응물1-(Pyridin-3-yl)imidazolidin-2-oneHCID 14834204—
촉매Copper iodideHCID 83717—
용매1,4-DioxaneHCID 31275—
생성물1-(1-Oxo-indan-5-yl)-3-pyridin-3-yl-imidazolidin-2-oneHCID 5963613361.72%

반응 단계

Using the same reaction conditions as in Example 1, 1-pyridin-3-yl-imidazolidin-2-one (I-1b: 270 mg, 1.6587 mmol) was reacted with 5-bromo-indan-1-one (350 mg, 1.6587 mmol), 1,4-dioxane (10 mL), copper iodide (31.59 mg, 0.165879 mmol), trans-1,2-diamino cyclohexane (56.976 mg, 0.4976 mmol) and potassium carbonate (458.63 mg, 3.3174 mmol) to afford the crude product. Purification by column chromatography on silica gel (1% MeOH in chloroform) afforded 300 mg of 1-(1-oxo-indan-5-yl)-3-pyridin-3-yl-imidazolidin-2-one (61.72% yield). Hydroxylamine hydrochloride (141 mg, 2.044 mmol) and sodium acetate (167.6 mg, 2.044 mmol) in 5 mL of water were added to a solution of 1-(3-oxo-indan-5-yl)-3-pyridin-3-yl-imidazolidin-2-one (200 mg, 0.6814 mmol) in ethanol (7 mL). The reaction mixture was heated to 90° C. and maintained for 6 hours. The reaction mixture was then cooled to room temperature and the solvent was distilled from the reaction mixture. The precipitate formed was collected, washed with chloroform and dried under reduced pressure to afford 200 mg of the product (90% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-7803d0f8c11741839bfe5d18831ad9f3
출처 메모uspto-grants-2014_09