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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535650생성일: 2026년 10월 24일

Cesium carbonate → Ethyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylate

https://huagongshe.com/ko/reaction/535650

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물Ethyl 7-bromobenzofuran-2-carboxylateHCID 46738833—
반응물1-(5-(2-(Piperazin-1-yl)ethyl)indolin-1-yl)ethanoneHCID 59636747—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
생성물Ethyl 7-(4-(2-(1-acetylindolin-5-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxylateHCID 5963675661.5%

반응 조건

온도95 °C

반응 단계

Cesium carbonate (0.724 g, 2.22 mmol), 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (0.081 g, 0.17 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.078 g, 0.09 mmol) were added under argon to a mixture of ethyl 7-bromobenzofuran-2-carboxylate (0.460 g, 1.71 mmol) and 1-(5-(2-(piperazin-1-yl)ethyl)indolin-1-yl)ethanone (0.491 g, 1.79 mmol) (example 38c) in dry degassed dioxane (8 mL) and the reaction was heated at 95° C. over night. After cooling to room temperature, water and DCM were added and the layers separated. The aq phase was extracted with DCM (3×). The combined organic phases were washed with water, dried (MgSO4), filtered and evaporated. The crude product was purified by flash chromatography (DCM/MeOH 95/5) to give 0.485 g (61%) of the product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859534B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-3830199987214ab39ba092e1b152b6df
출처 메모uspto-grants-2014_10