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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17595생성일: 2026년 10월 23일

2,6-Di-tert-butyl-4-methylphenol → 2-Cyclopropyl-7-fluoro-5-methyl-6-(thiophen-2-yl)-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17595

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Di-tert-butyl-4-methylphenolHCID 31404—
반응물2-(Tri-n-butylstannyl)thiopheneHCID 2779373—
반응물6-Bromo-2-cyclopropyl-7-fluoro-5-methylbenzoxazole-4-carbonitrileHCID 51041427—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물2-Cyclopropyl-7-fluoro-5-methyl-6-(thiophen-2-yl)-1,3-benzoxazole-4-carbonitrileHCID 6858597696%

반응 조건

온도100 °C

반응 단계

6-Bromo-2-cyclopropyl-7-fluoro-5-methyl-1,3-benzoxazole-4-carbonitrile (I-77) (200 mg, 0.68 mmol), 2-(tri-n-butylstannyl)thiophene (280 μl, 0.88 mmol) and 2,6-di-tert-butyl-p-cresol (2 grains) were dissolved in 1,4-dioxane (6 ml), and at room temperature, bis(triphenylphosphine)palladium(II) dichloride (48 mg, 0.07 mmol) was added. The solution was stirred under nitrogen atmosphere at 100° C. for 15 hours. After cooling to room temperature, the insoluble matter was separated by filtration with washing with ethyl acetate. The filtrate was washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, n-hexane:ethyl acetate=19:1, v/v) to obtain the entitled compound (194 mg, 96%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-c6b8eaf62198449dbc98ea4404329060
출처 메모uspto-grants-2010_06