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HRID 217作成日:2026年10月23日

Piperazine → 4-Piperazin-1-yl-1-benzofuran-2-carboxamide

https://huagongshe.com/ja/reaction/217

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物4-Bromo-1-benzofuran-2-carboxamideHCID 112520563—
試薬Cesium carbonateHCID 10796—
触媒Binap, (A+-)-HCID 634876—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TetrahydrofuranHCID 8028—
生成物4-Piperazin-1-yl-1-benzofuran-2-carboxamideHCID 111959390%

反応条件

温度70 °C

反応手順

The crude product from EN03731-54-001, 4-bromobenzofuran-2-carboxamide (0.600 g, 2.5 mmol), was dissolved in THF (18 mL) and water (18.00 mL). To this mixture were added piperazine (1.077 g, 12.50 mmol), Cesium carbonate (1.629 g, 5.00 mmol), Tris(dibenzylideneacetone)dipalladium(0) (0.114 g, 0.13 mmol) and rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.156 g, 0.25 mmol) and the reaction was heated at 70 °C over night. 2010-04-13 No product was detected. The reaction mixture was filtered and solvents were removed in vacuo. The residue was partitioned between methylene chloride and water. The organic layer was washed with 1M HCl(aq), dired with sodium sulfate, filtered, concentrated and purified by flash chromatography(Isolute Si 70g, methylene chloride: methanol; 97:3). No product could be detected/isolated.

情報源と証拠

出典データセット750 AstraZeneca ELN dataset
ORD IDord-dc56e46e611f4db1889616d29baeeb5f
出典メモ750 AstraZeneca ELN dataset