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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1435719생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1435719

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 번호US07618969B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-48b958e56b0244709af1e893d0ddc2f8
출처 메모uspto-grants-2009_11