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HRID 1645280생성일: 2026년 10월 24일

Water → Methyl 4-(5-((5-chloro-2-oxoindolin-3-ylidene)methyl)furan-2-yl)-3-fluorobenzoate

https://huagongshe.com/ko/reaction/1645280

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물2-Fluoro-4-(methoxycarbonyl)benzeneboronic acidHCID 24824345—
반응물3-((5-Bromofuran-2-yl)methylene)-5-chloroindolin-2-oneHCID 66772829—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매1,4-Dioxane--water (1/1)HCID 21886435—
생성물Methyl 4-(5-((5-chloro-2-oxoindolin-3-ylidene)methyl)furan-2-yl)-3-fluorobenzoateHCID 66772791—

반응 조건

온도110 °C

반응 단계

To 3-((5-bromofuran-2-yl)methylene)-5-chloroindolin-2-one (150 mg, 0.466 mmol) in dioxane/water (2850/150 μL) was added 2-fluoro-4-(methoxycarbonyl)phenylboronic acid (111 mg, 0.559 mmol) and Cs2CO3 (456 mg, 1.398 mmol). The mixture was degassed with nitrogen for 5 minutes, then PdCl2 dppf (17 mg, 0.023 mmol) was added. The mixture was heated in microwave for 40 minutes at 110° C. Water was added and the solid formed was isolated by filtration to yield methyl 4-(5-((5-chloro-2-oxoindolin-3-ylidene)methyl)furan-2-yl)-3-fluorobenzoate. LCMS (M+1=398).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08124649B2
출처 데이터셋uspto-grants-2012_02
ORD IDord-b955915415f340128430572236e447bc
출처 메모uspto-grants-2012_02