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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 217생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물4-Bromo-1-benzofuran-2-carboxamideHCID 112520563—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TetrahydrofuranHCID 8028—
생성물4-Piperazin-1-yl-1-benzofuran-2-carboxamideHCID 111959390%

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-dc56e46e611f4db1889616d29baeeb5f
출처 메모750 AstraZeneca ELN dataset