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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70611생성일: 2026년 10월 25일

Cesium carbonate → 3-chloro-2-methoxy-6-[(E)-1-[4-(propan-2-yl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethenyl]pyridine

https://huagongshe.com/reaction/70611

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Tris(furan-2-yl)phosphaneHCID 521585—
반응물4-Isopropylphenylboronic acidHCID 2773480—
반응물6-[(Z)-1-bromo-2-(tetrahydro-2H-pyran-4-yl)ethenyl]-3-chloro-2-methoxypyridineHCID 58452513—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물3-chloro-2-methoxy-6-[(E)-1-[4-(propan-2-yl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethenyl]pyridineHCID 67396409—

반응 조건

온도90 °C

반응 단계

4-Isopropylphenylboronic acid (103 mg), tris(dibenzylideneacetone)dipalladium (38 mg), tri(2-furyl)phosphine (58 mg), cesium carbonate (273 mg) and water (0.5 mL) were added to a solution of 6-[(Z)-1-bromo-2-(tetrahydro-2H-pyran-4-yl)ethenyl]-3-chloro-2-methoxypyridine (140 mg) in 1,4-dioxane (3 mL), and the mixture was stirred at 90° C. for two hours. The reaction solution was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1→1:1) to give 3-chloro-2-methoxy-6-[(E)-1-[4-(propan-2-yl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethenyl]pyridine containing impurities as a yellow oil (170 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-a7091b02514d44df8b669a8650c38874
출처 메모uspto-grants-2014_09