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HRID 318作成日:2026年10月23日

Piperazine → 4-Fluoro-2-(piperazin-1-yl)benzonitrile

https://huagongshe.com/ja/reaction/318

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物2-Bromo-4-fluorobenzonitrileHCID 118939—
試薬Cesium carbonateHCID 10796—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒1,4-DioxaneHCID 31275—
生成物4-Fluoro-2-(piperazin-1-yl)benzonitrileHCID 193671080%

反応条件

温度90 °C

反応手順

Tris(dibenzylideneacetone)dipalladium (0) (57.2 mg, 0.06 mmol) and rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (78 mg, 0.12 mmol) were added to a mixture of 2-bromo-4-fluorobenzonitrile (250 mg, 1.25 mmol), Cesium carbonate (611 mg, 1.87 mmol) and Piperazine (215 mg, 2.50 mmol) in dioxane (3 mL). Reaction vessel was placed in an oil bath at 90 °C 4pm. LCMS o/n shows several peaks. Larger peak corresponding to displacement of F by piperazine (MW266) than for desired product (205). Discarded

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-91c1aa5c02fc46a586e9f5a373b7526a
出典メモ750 AstraZeneca ELN dataset