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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 627480생성일: 2026년 10월 25일

1-Methylimidazole → (1-Methyl-1H-imidazol-5-yl)(pyridin-3-yl)methanone

https://huagongshe.com/reaction/627480

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylimidazoleHCID 1390—
반응물HexaneHCID 8058—
반응물ChlorotriethylsilaneHCID 13819—
반응물N-Methoxy-N-methylnicotinamideHCID 10558996—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물(1-Methyl-1H-imidazol-5-yl)(pyridin-3-yl)methanoneHCID 82895938—

반응 조건

온도-78 °C

반응 단계

To a heat-gun dried flask containing 1-methyl-1H-imidazole (1.55 mL, 19.5 mmol) and THF (20 mL) at −78° C. was added 1.6 M n-BuLi in hexane (12.8 mL, 20.5 mmol). After stirring at −78° C. for 30 min, chlorotriethylsilane (3.3 mL, 19.7 mmol) in neat was introduced slowly. The mixture was stirred at −78° C. for 30 min. 1.6 M n-BuLi in hexane (12.8 mL, 20.5 mmol) was added, and the mixture was stirred for 45 min. A solution of N-methoxy-N-methylnicotinamide (2.70 g, 16.2 mmol, Intermediate 10, step a) in THF (20 mL) was added via cannula, and the mixture was stirred at −78° C. to room temperature for 2 hours. The reaction was quenched with NH4Cl (aqueous), the organic layer was separated, and the aqueous layer was extracted with CH2Cl2. The combined organic phases were dried (Na2SO4), filtered, concentrated, and purified by flash column chromatography (40 g silica gel column, 50-100% EtOAc in heptane, then 5-10% MeOH in CH2Cl2) to obtain the title compound as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09309222B2
출처 데이터셋uspto-grants-2016_04
ORD IDord-eeb3e72309854c1481afc181307a9eb0
출처 메모uspto-grants-2016_04