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HRID 447813作成日:2026年10月25日

Potassium Carbonate → 5-Chloro-2-imino-1-[2-(methylsulfonyl)-5-(trifluoromethyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochloride

https://huagongshe.com/reaction/447813

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 HydroxideHCID 14798—
反応物2-Cyano-2-(3,4-dichloro-5(2H)-oxo-2-furyl)acetamideHCID 541792—
反応物1-[2-(Methylsulfonyl)-5-(trifluoromethyl)phenyl]methanamine hydrochlorideHCID 66877167—
溶媒EthanolHCID 702—
生成物5-Chloro-2-imino-1-[2-(methylsulfonyl)-5-(trifluoromethyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochlorideHCID 6696990162.6%

反応手順

(Step 4) 2-Cyano-2-(3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)acetamide (1.69 g), 1-[2-(methylsulfonyl)-5-(trifluoromethyl)phenyl]methanamine hydrochloride obtained in Step 3 (2.5 g) and potassium carbonate (2.98 g) were stirred in ethanol (30 ml) at 80° C. for 16 hr. The reaction mixture was treated with 1N sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:hexane=4:1). The obtained residue was dissolved in methanol, 4N hydrogen chloride-ethyl acetate solution (5 ml) was added, and the mixture was crystallized from methanol-ethyl acetate. The precipitated crystals were collected by filtration, and recrystallized to give the title compound (1.0 g)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481569B2
出典データセットuspto-grants-2013_07
ORD IDord-579151e1cf704dbaa6979edcd65fe629
出典メモuspto-grants-2013_07