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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 535680생성일: 2026년 10월 24일

Piperazine, 2-pyridylethyl- → 5-Methoxy-N,N-dimethyl-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/ko/reaction/535680

반응식

참여 물질

역할이름HCID투입량
반응물Piperazine, 2-pyridylethyl-HCID 566605—
반응물2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
반응물Sodium t-butoxideHCID 23676156—
반응물7-Bromo-5-methoxy-N,N-dimethylbenzofuran-2-carboxamideHCID 59636744—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물5-Methoxy-N,N-dimethyl-7-(4-(2-(pyridin-2-yl)ethyl)piperazin-1-yl)benzofuran-2-carboxamideHCID 59636711—

반응 단계

7-Bromo-5-methoxy-N,N-dimethylbenzofuran-2-carboxamide (0.20 g, 0.67 mmol), 1-(2-pyridin-2-yl-ethyl)piperazine (0.13 g, 0.67 mmol), Pd2 dba3 (0.031 g, 0.030 mmol), 2-dicyclohexylphosphino-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (0.032 g, 0.070 mmol) and sodium t-butoxide (0.14 g, 1.41 mmol) were heated in toluene (1 mL) at 100° C. for 2 h. The mixture was allowed to cool. Ethyl acetate was added and the mixture was filtered through a pad of celite. The filtrate was washed with water and brine, dried over MgSO4 and the solvent was removed by rotary evaporation. The crude product was purified by flash chromatography (SiO2; DCM/MeOH; gradient 0-3%) to give the title compound. Yield: 0.14 g (52%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859534B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-e8ee74b43f8e49dc9f0fc656bba9c955
출처 메모uspto-grants-2014_10