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HRID 2100699作成日:2026年10月26日

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

https://huagongshe.com/reaction/2100699

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物TriphenylphosphineHCID 11776—
反応物2-Fluoropyridine-3-boronic acidHCID 2783270—
反応物N-(5-iodo-2,3-dihydro-1H-inden-2-yl)-2-propanesulfonamideHCID 46899809—
触媒PalladiumHCID 23938—
触媒palladium(II) acetateHCID 167845—
溶媒1,4-DioxaneHCID 31275—
生成物N-[5-(2-fluoro-3-pyridinyl)-2,3-dihydro-1H-inden-2-yl]-2-propanesulfonamideHCID 1170976237%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07572819B2
出典データセットuspto-grants-2009_08
ORD IDord-6e6c4d9543bf4da5846922de8f093690
出典メモuspto-grants-2009_08