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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32721생성일: 2026년 10월 24일

Hydrochloric Acid → 1-{4-[4-(5-Acetyl-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-3-fluoro-phenyl}-ethanone

https://huagongshe.com/ko/reaction/32721

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Stannane, tributyl(1-ethoxyethenyl)-HCID 619414—
반응물1-(4-(4-(5-Bromo-2-morpholinobenzoyl)piperazin-1-yl)-3-fluorophenyl)ethanoneHCID 44580513—
촉매HCID 178418476HCID 178418476—
용매TolueneHCID 1140—
생성물1-{4-[4-(5-Acetyl-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-3-fluoro-phenyl}-ethanoneHCID 5979355210%

반응 단계

To a suspension of 1-{4-[4-(5-Bromo-2-morpholin-4-yl-benzoyl)-piperazin-1-yl]-3-fluoro-phenyl}-ethanone (160 mg, 0.33 mmol) in toluene (2 ml) were added PdCl2(PPh3)2 (5 mg, 0.0065 mmol) and tributyl(1-ethoxyvinyl)tin (125 ul, 0.36 mmol). The mixture was heated to 100IC for 6 hours. The mixture was cooled in an ice bath and 2N HCl (0.55 ml) was added. The mixture was stirred at room temperature overnight. The mixture was filtered. The organic layer was separated and 10% aqueous KF solution was added. The mixture was stirred at room temperature for 3 hours and filtered. The organic layer was dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude gum was chromatographed on silica gel, eluent: heptane/ethylacetate 0%-50% (10 minutes) to provide the title compound (15 mg, 10%) as a white solid MS (m/e): 454.2 (M+H, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427612B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-eed712f9c61f4c4292769ab9933e2c88
출처 메모uspto-grants-2008_09