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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1510589생성일: 2026년 10월 26일

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/1510589

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Fluoro-4-methylanilineHCID 67984—
반응물4-chloro-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dioneHCID 66673372—
반응물(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthylHCID 86595863—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물4-(2-fluoro-4-methylphenylamino)-1,3,8-trimethyl-1H,6H-pyrido[2,3-d]pyridazine-2,5-dioneHCID 57636929—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08211921B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-c30555f8f00c4c77a7d67257bd60bf57
출처 메모uspto-grants-2012_07