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HRID 15931作成日:2026年10月26日

Cesium carbonate → 4-(2-Fluoro-4-methylphenylamino)-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/15931

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2-Fluoro-4-methylanilineHCID 67984—
反応物4-Chloro-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl esterHCID 66673972—
反応物(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthylHCID 86595863—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2-Fluoro-4-methylphenylamino)-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl esterHCID 6667463171%

反応条件

温度80 °C

反応手順

2-Fluoro-4-methylphenylamine (0.259 g, 2.07 mmol), palladium (II) acetate (0.046 g, 0.205 mmol), rac-2,2-bis(diphenylphosphino)-1,1′-binaphthyl (0.192 g, 0.308 mmol), and cesium carbonate (1.00 g, 3.08 mmol) were added to a solution of 4-chloro-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester (0.50 g, 2.05 mmol) in toluene (7 mL) in a sealed vial. After stirring 10 minutes, the mixture was heated to 80° C. After 24 hours, the reaction mixture was cooled to room temperature and diluted with EtOAc. The resulting precipitate was filtered and washed with EtOAc. The filtrate was diluted with EtOAc and washed with water. The aqueous layer was reextracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and concentrated. Purification by flash column chromatography (20:1 methylene chloride/MeOH) gave 0.048 g (71%) desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732616B2
出典データセットuspto-grants-2010_06
ORD IDord-e69eff02af2941c1807202bb1f188821
出典メモuspto-grants-2010_06