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HRID 524344作成日:2026年10月25日

Potassium Carbonate → 1-Isopropyl-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4]bipyridinyl-5-carboxylic acid 4-methanesulfonyl-benzylamide

https://huagongshe.com/reaction/524344

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2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
反応物HCID 86711578HCID 86711578—
溶媒AcetonitrileHCID 6342—
生成物1-Isopropyl-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4]bipyridinyl-5-carboxylic acid 4-methanesulfonyl-benzylamideHCID 73296271—

反応条件

温度75 °C

反応手順

To a solution of 5-bromo-1-isopropyl-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (preparation 5, 24 mg, 0.054 mmol), 2-(trifluoromethyl)pyridine-4-boronic acid (13 mg, 0.068 mmol), 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (5 mg, 0.007 mmol) in acetonitrile (0.15 mL) is added 2 M aqueous K2CO3 solution (0.055 mL, 0.11 mmol). After stirring for 18 h at 75° C., the reaction mixture is filtered and purified by preparative reversed-phase HPLC (XBridge, gradient of methanol in water, 0.3% NH4OH, 60° C.). Yield: 4 mg (15% of theory); ESI mass spectrum: [M+H]+=508; Retention time HPLC: 0.88 min (Z003_001).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09340507B2
出典データセットuspto-grants-2016_05
ORD IDord-310879f39c7440c39cc8a647db580f9c
出典メモuspto-grants-2016_05