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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2363705생성일: 2026년 10월 24일

Dabco → 6-(3-furyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/ko/reaction/2363705

반응식

참여 물질

역할이름HCID투입량
반응물DabcoHCID 9237—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Triethoxy(furan-3-yl)silaneHCID 12556749—
반응물6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771673—
촉매palladium(II) acetateHCID 167845—
용매TetrahydrofuranHCID 8028—
용매1,4-DioxaneHCID 31275—
생성물6-(3-furyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 44137766—

반응 단계

200 mg of 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 1), 10 mL of dioxane, 400 μL of 3-(triethoxysilyl)furan, 42 mg of palladium acetate, 42 mg of 1,4-diazabicyclo(2.2.2)octane (DABCO) and 1.5 mL of a molar solution of tetrabutylammonium fluoride in tetrahydrofuran are placed in a microwave tube. The reaction mixture is heated for 3 hours in a microwave machine set at 120° C., 200 μL of 3-(triethoxysilyl)furan, 20 mg of palladium acetate and 20 mg of DABCO are then added and the mixture is heated for a further 1.5 hours in a microwave machine set at 150° C. and then cooled and filtered. The filtrate is concentrated to dryness under reduced pressure and the residue is chromatographed on a silica cartridge, eluting with dichloromethane. The fractions containing the pure expected product are combined and evaporated to dryness under reduced pressure. The solid is dissolved while hot in a mixture of dichloromethane and methanol. The hot solution is filtered and treated with diisopropyl ether. The precipitate formed is filtered off by suction and dried to give 25 mg of 6-(3-furyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691990B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-46d882a1d08c4733a9540da3f17e17e4
출처 메모uspto-grants-2014_04