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HRID 15954作成日:2026年10月26日

Cesium carbonate → 4-(2-fluoro-4-methylphenylamino)-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dione

https://huagongshe.com/reaction/15954

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-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dioneHCID 66673372—
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)-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dioneHCID 57636929—

反応条件

温度80 °C

反応手順

2-Fluoro-4-methylphenylamine (1.10 equivalents), palladium (II) acetate (0.10 equivalents), rac-2,2-bis(diphenylphosphino)-1,1′-binaphthyl (0.15 equivalents), and cesium carbonate (1.50 equivalents) are added to a solution of 4-chloro-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dione (1.00 equivalent) in toluene in a sealed vial. After stirring 10 minutes, the mixture is heated to 80° C. After 24 hours, the reaction mixture is cooled to room temperature and diluted with EtOAc. The resulting precipitate is filtered and washed with EtOAc. The filtrate is diluted with EtOAc and washed with water. The aqueous layer is reextracted with EtOAc. The combined organic layers are washed with brine, dried (Na2SO4) and concentrated. Purification by flash column chromatography gives the 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-ac4da3a781684744ac00ba4f98539037
出典メモuspto-grants-2010_06