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HRID 512503作成日:2026年10月25日

Potassium Carbonate → 1-[1-(4-Cyano-phenyl)-ethyl]-5-(3-difluoromethyl-phenyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid methylamide

https://huagongshe.com/reaction/512503

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3-Difluoromethyl-phenylboronic acidHCID 44717244—
反応物5-Bromo-1-[1-(4-cyano-phenyl)-ethyl]-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid methylamideHCID 86711537—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒AcetonitrileHCID 6342—
生成物1-[1-(4-Cyano-phenyl)-ethyl]-5-(3-difluoromethyl-phenyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid methylamideHCID 73426830—

反応条件

温度75 °C

反応手順

To a solution of 5-bromo-1-[1-(4-cyano-phenyl)-ethyl]-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid methylamide (preparation 9, 100 mg, 0.267 mmol), 3-difluoromethyl-phenylboronic acid (67 mg, 0.390 mmol), palladium (0) tetrakis(triphenylphosphine) (25 mg, 0.022 mmol) in acetonitrile (2 mL) is added 2 M aqueous K2CO3 solution (0.30 mL, 0.60 mmol). After stirring for 18 h at 75° C., the reaction mixture is purified by preparative reversed-phase HPLC (XBridge, gradient of methanol in water, 0.1% NH4OH, 60° C.). Yield: 80 mg (71% of theory); ESI mass spectrum: [M+H]+=422; Retention time HPLC: 0.99 min (Z018_S04).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102624B2
出典データセットuspto-grants-2015_08
ORD IDord-d4e8b9451ee44f71b9245682c59a86ec
出典メモuspto-grants-2015_08