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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2357561생성일: 2026년 10월 27일

Potassium Carbonate → N-cyclopropyl-3-(1-(2,4-dimethylphenyl)phthalazin-6-yl)-4-methylbenzamide

https://huagongshe.com/reaction/2357561

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(Dicyclohexylphosphino)-2'-methylbiphenylHCID 2734938—
반응물N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamideHCID 21914577—
반응물6-chloro-1-(2,4-dimethylphenyl)PhthalazineHCID 68454866—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매MethanolHCID 887—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물N-cyclopropyl-3-(1-(2,4-dimethylphenyl)phthalazin-6-yl)-4-methylbenzamideHCID 68452425—

반응 단계

A mixture of 6-chloro-1-(2,4-dimethylphenyl)phthalazine (150 mg, 558 μmol), N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (437 mg, 1450 μmol), 2-(dicyclohexylphosphino)-2′-methylbiphenyl (18.3 mg, 50.2 μmol, Strem), Pd2(dba)3 (15.3 mg, 16.7 μmol, Strem), and potassium carbonate (231 mg, 1674 μmol) in Dioxane:H2O=4:1 (5 mL) was heated to 80° C. for 18 h. After cooling to room temperature, the mixture was diluted with MeOH and concentrated over SiO2. The residue was purified with column chromatography (MeOH/CH2Cl2=0-4%). The residue was purified with reverse-phase chromatography (Phenomenex Synergi 4m Max RP 80 A column, 150×21 mm, 20 mL/min, 10-95% CH3CN/H2O, 0.1% TFA, 10.5 min gradient). Yield: 113 mg (50%). MS (ESI, pos. ion) m/z: 408 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07759337B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-0a582763ec8c4a5d9a829294ca033bc5
출처 메모uspto-grants-2010_07