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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Tris(furan-2-yl)phosphane | HCID 521585 | — |
| 반응물 | 4-Isopropylphenylboronic acid | HCID 2773480 | — |
| 반응물 | 6-[(Z)-1-bromo-2-(tetrahydro-2H-pyran-4-yl)ethenyl]-3-chloro-2-methoxypyridine | HCID 58452513 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 3-chloro-2-methoxy-6-[(E)-1-[4-(propan-2-yl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethenyl]pyridine | HCID 67396409 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08822503B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-a7091b02514d44df8b669a8650c38874 |
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| 출처 메모 | uspto-grants-2014_09 |
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