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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2100699생성일: 2026년 10월 25일

Cesium carbonate → N-[5-(2-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamide

https://huagongshe.com/reaction/2100699

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물TriphenylphosphineHCID 11776—
반응물2-Fluoropyridine-3-boronic acidHCID 2783270—
반응물N-(5-iodo-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 46899809—
촉매PalladiumHCID 23938—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물N-[5-(2-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamideHCID 1170976237%

반응 단계

A mixture of Intermediate 2 (65 mg, 0.18 mmol) and cesium carbonate (1.5 eq, 88 mg, 0.27 mmol) in a 3:1 mixture of 1,4-dioxan:water (4 ml) was degassed with argon for 5 minutes. Then the mixture was added to (2-fluoro-3-pyridinyl)boronic acid (1.1 eq, 28 mg, 0.20 mmol, Asymchem International Inc.). Palladium acetate (2 mg, 0.01 mmol—alternatively, solid supported palladium may be used), and triphenylphosphine (9 mg, 0.03 mmol) were then added and the whole mixture stirred at reflux for 16 h. The reaction mixture was allowed to cool and partitioned between ethyl acetate (10 ml) and water (10 ml). The organic layer was separated, dried and evaporated. The resulting product was purified using mass directed preparative HPLC to give the title compound (22 mg, 37%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572819B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-6e6c4d9543bf4da5846922de8f093690
출처 메모uspto-grants-2009_08