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HRID 2178107作成日:2026年10月26日

Potassium Carbonate → URAT1 inhibitor 7

https://huagongshe.com/reaction/2178107

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Sodium BicarbonateHCID 516892—
反応物2-Chloro-4-hydroxybenzonitrileHCID 592797—
反応物3-cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamideHCID 59436600—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物URAT1 inhibitor 7HCID 8629466346%

反応条件

温度80 °C

反応手順

3-Cyano-4-fluoro-N-(5-fluoropyridin-2-yl)benzenesulfonamide (Preparation 2, 10.5 g, 35.6 mmol) was added to a solution of 2-chloro-4-hydroxybenzonitrile (8.19 g, 53.3 mmol) and potassium carbonate (14.74 g, 106.7 mmol) in dimethylsulfoxide (100 mL) at room temperature. The resulting mixture was stirred at 80° C. for 44 hours. On cooling, the reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution (200 mL) and ethyl acetate (1000 mL) was added. The aqueous layer was separated and the organic layer was washed with saturated aqueous sodium hydrogen carbonate solution (3×200 mL), water (2×200 mL) and brine (2×200 mL). The organic layer was dried over sodium sulphate, filtered and concentrated in vacuo. The residue was purified by reverse phase column chromatography eluting with acetonitrile (containing 0.1% HCO2H): water (containing 0.1% HCO2H) from 0 to 100% to afford the title compound as a white solid (6.982 g, 46%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09067922B2
出典データセットuspto-grants-2015_06
ORD IDord-be6b74a1d1394616becd589715437aba
出典メモuspto-grants-2015_06