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HRID 1645280作成日:2026年10月26日

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

https://huagongshe.com/reaction/1645280

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Cesium carbonateHCID 10796—
反応物2-Fluoro-4-(methoxycarbonyl)benzeneboronic acidHCID 24824345—
反応物3-((5-Bromofuran-2-yl)methylene)-5-chloroindolin-2-oneHCID 66772829—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒1,4-Dioxane--water (1/1)HCID 21886435—
生成物Methyl 4-(5-((5-chloro-2-oxoindolin-3-ylidene)methyl)furan-2-yl)-3-fluorobenzoateHCID 66772791—

反応条件

温度110 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08124649B2
出典データセットuspto-grants-2012_02
ORD IDord-b955915415f340128430572236e447bc
出典メモuspto-grants-2012_02