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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 454867생성일: 2026년 10월 24일

5-Fluoro-o-toluidine → 1-(4-fluoro-2-methylphenyl)-N-(5-fluoro-2-methylphenyl)phthalazin-6-amine

https://huagongshe.com/ko/reaction/454867

반응식

참여 물질

역할이름HCID투입량
반응물5-Fluoro-o-toluidineHCID 67774—
반응물Dicyclohexyl(2',4',6'-tripropyl-[1,1'-biphenyl]-2-yl)phosphineHCID 21081571—
반응물Sodium t-butoxideHCID 23676156—
반응물6-Chloro-1-(4-fluoro-2-methylphenyl)phthalazineHCID 66739677—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물1-(4-fluoro-2-methylphenyl)-N-(5-fluoro-2-methylphenyl)phthalazin-6-amineHCID 45280128—

반응 조건

온도100 °C

반응 단계

A mixture of 6-chloro-1-(4-fluoro-2-methylphenyl)phthalazine (200 mg, 0.73 mmol), 5-fluoro-2-methylaniline (138 mg, 1.1 mmol), tris(dibenzylideneacetone)dipalladium (0) (34 mg, 0.037 μmol), 2-(dicyclohexylphosphino)-2′,4′,6′-tri-1-propyl-1,1′-biphenyl (35 mg, 0.073 mmol), and sodium tert-butoxide (211 mg, 2.2 mmol) in toluene (2 mL) was heated at 100° C. in an oil bath for 18 h. The mixture was cooled to room temperature, diluted with MeOH and filtered through a pad of Celite. The filtrate was concentrated over silica gel and purified using column chromatography (0-40% acetone in hexanes) to afford a tan solid that was about 90% pure. The material was dissolved in MeOH and loaded onto an Agilent AccuBOND II SCX solid phase extraction column. It was washed with MeOH followed by 2 M NH3 in MeOH. The title compound was obtained as a tan solid. MS (ESI, pos. ion) m/z: 362.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497269B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-299e22a496894bfda0b4ec1b02af75f7
출처 메모uspto-grants-2013_07