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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 333725생성일: 2026년 10월 26일

Potassium Carbonate → 1-benzyl-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one

https://huagongshe.com/reaction/333725

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물1-Phenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 58072367—
반응물1-benzyl-3-chloro-5-methoxypyridazin-4(1H)-oneHCID 86686560—
촉매Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II)HCID 11714597—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Sodium BicarbonateHCID 516892—
생성물1-benzyl-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-oneHCID 6801490577.7%

반응 단계

1-Benzyl-3-chloro-5-methoxypyridazin-4(1H)-one (13.6 g), 1-phenyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (22.0 g), potassium carbonate (51.0 g) and bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) (1.92 g) were suspended in toluene (330 mL) and water (33.0 mL), and the mixture was heated under reflux under a nitrogen atmosphere for 24 hr. The reaction mixture was cooled to room temperature, diluted with water and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated, and the residue was recrystallized from ethyl acetate/hexane to give the title compound (15.1 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883788B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-ab5526d7195b454ba88b324db14c005d
출처 메모uspto-grants-2014_11