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HRID 1969441作成日:2026年10月26日

Cesium carbonate → Ethyl 5-fluoro-4-oxo-1-[4-(4-vinyl-1H-pyrazol-1-yl)benzyl]-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/1969441

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Potassium vinyltrifluoroborateHCID 23679353—
反応物ethyl 5-fluoro-1-[4-(4-iodo-1H-pyrazol-1-yl)benzyl]-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 58297053—
触媒HCID 178454917HCID 178454917—
溶媒AcetonitrileHCID 6342—
生成物Ethyl 5-fluoro-4-oxo-1-[4-(4-vinyl-1H-pyrazol-1-yl)benzyl]-1,4-dihydroquinoline-3-carboxylateHCID 44623933—

反応条件

温度100 °C

反応手順

To a solution of ethyl 5-fluoro-1-[4-(4-iodo-1H-pyrazol-1-yl)benzyl]-4-oxo-1,4-dihydroquinoline-3-carboxylate (0.080 g, 0.15 mmol), potassium vinyltrifluoroborate (0.013 g, 0.19 mmol), and 1 N cesium carbonate (0.31 mL, 0.31 mmol) in 2 mL of acetonitrile under nitrogen was added bis(tri-tert-butylphosphoranyl)palladium (10 mol %). The reaction mixture was stirred at 100° C. for 14 hours, cooled to room temperature, and concentrated in vacuo to provide the title compound (crude) which gave a mass ion (ES+) of 417.9 for M+H+. This compound could be further hydrolyzed to the corresponding carboxylic acid, as described in Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08426598B2
出典データセットuspto-grants-2013_04
ORD IDord-c315ae412dc74745811454f878483126
出典メモuspto-grants-2013_04