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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80040생성일: 2026년 10월 24일

1,2-Diaminocyclohexane, trans- → 1-(4-Methyl-pyridin-3-yl)-3-(5-methyl-thiophen-2-yl)-imidazolidin-2-one

https://huagongshe.com/ko/reaction/80040

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Diaminocyclohexane, trans-HCID 43806—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-Bromo-5-methylthiopheneHCID 69831—
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-(5-methyl-thiophen-2-yl)-imidazolidin-2-oneHCID 4987186774%

반응 조건

온도110 °C

반응 단계

Copper iodide (16 mg, 0.084 mmol), trans-1,2-diamino cyclohexane (28.8 mg, 0.25 mmol) and potassium phosphate (445 mg, 2.1 mmol) were added to 1,4-Dioxane (10 mL) previously degassed with argon (10 minutes). The reaction mixture was purged with argon for a further 10 minutes, followed by the addition of 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.84 mmol) and 2-bromo-5-methylthiophene (150 mg, 0.84 mmol). The resulting mixture was heated to reflux at 110° C. for 4 hours. The reaction was monitored by TLC (10% MeOH in chloroform). The reaction mixture was filtered through celite and the celitebed was washed with chloroform. The organic layer was dried over Na2SO4 and concentrated. The concentrate was quenched with ice, the precipitate formed was collected and dried to afford 170 mg (74% yield) of 1-(4-methyl-pyridin-3-yl)-3-(5-methyl-thiophen-2-yl)-imidazolidin-2-one.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-9d155cf1125b484f9d5ab50ed4b67e28
출처 메모uspto-grants-2014_09