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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 23553생성일: 2026년 10월 26일

Water → 8-(2,4-Dichlorophenyl)-4-(4-isopropyloxycarbonyl-1,2,3,6-tetrahydropyridin-1-yl)-2-methylquinoline

https://huagongshe.com/reaction/23553

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium CarbonateHCID 10340—
반응물2,4-Dichlorophenylboric acidHCID 21984477—
반응물8-Bromo-4-(4-isopropyloxycarbonyl-1,2,3,6-tetrahydropyridin-1-yl)-2-methylquinolineHCID 22574430—
촉매HCID 178418397HCID 178418397—
용매EthanolHCID 702—
용매TolueneHCID 1140—
생성물8-(2,4-Dichlorophenyl)-4-(4-isopropyloxycarbonyl-1,2,3,6-tetrahydropyridin-1-yl)-2-methylquinolineHCID 12134673—

반응 단계

Under a nitrogen atmosphere, 8-bromo-4-(4-isopropyloxycarbonyl-1,2,3,6-tetrahydropyridin-1-yl)-2-methylquinoline (5.9 g), 2,4-dichlorophenylboric acid (3.2 q) and sodium carbonate (4.8 g) were suspended in a mixed solvent of deaerated water (15 mL), toluene (7.5 mL) and ethanol (7.5 mL), followed by adding thereto tetrakis(triphenylphosphine)palladium (0.88 g), and the resulting mixture was heated under reflux for 5 hours. The reaction mixture was cooled to room temperature to be separated. After the aqueous phase was extracted with ethyl acetate, the combined organic phase was dried over anhydrous sodium sulfate. The desiccating agent was filtered off, after which the filtrate was concentrated under reduced pressure and the resultant residue was crystallized from diisopropyl ether. The crystals were collected by filtration and washed with a small amount of diisopropyl ether to obtain the title compound (5.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06852732B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-7e955de06d824248a5976996fed68917
출처 메모uspto-grants-2005_02