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HRID 6607生成日期:2026年10月23日

(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮 → N-[4-(1,3-dioxolyl)phenyl]isatin

https://huagongshe.com/zh-CN/reaction/6607

反应方程式

参与物

角色名称HCID投料
反应物(5BETA,17BETA)-17-羟基-17-(甲基-D3)-2'H-雄甾-2-烯并[3,2-C]吡唑-5'(1'H)-酮HCID 887—
反应物靛红HCID 7054—
反应物氢化钠HCID 24758—
催化剂碘化亚铜HCID 24350—
溶剂三氯甲烷HCID 6212—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物N-[4-(1,3-dioxolyl)phenyl]isatinHCID 22016430—

反应步骤

Isatin (1.88 g, 0.0128 mol) in anhydrous DMF (100 mL) was cooled in an ice-bath under nitrogen and treated with sodium hydride (0.3 g, 1 equivalent). The reaction was warmed to room temperature and stirred for 1 hour. It was then treated with 2-(4-bromophenyl)-1,3-dioxalane (2.83 g, 0.0124 mol) followed by CuI (4.71 g, 2 equivalents). This suspension was heated in an oil-bath at 135° C. under nitrogen for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. The resulting suspension was filtered and the filtrate was concentrated under reduced pressure. The residue was suspended in xylenes (100 mL) and evaporated to dryness. A thick, viscous oil was recovered which was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion, Rf (product)=0.91.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07083986B2
来源数据集uspto-grants-2006_08
ORD IDord-bee7a5bb378040a9ab29ac748036e612
来源说明uspto-grants-2006_08