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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17461생성일: 2026년 10월 23일

2,6-Lutidine → 2-Cyclopropyl-7-fluoro-6-formyl-5-methyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17461

반응식

참여 물질

역할이름HCID투입량
반응물2,6-LutidineHCID 7937—
반응물Sodium SulfiteHCID 24437—
반응물Sodium periodateHCID 23667635—
반응물2-Cyclopropyl-7-fluoro-5-methyl-6-vinyl-1,3-benzoxazoleHCID 86630851—
촉매Osmium TetroxideHCID 30318—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매1,4-DioxaneHCID 31275—
용매Sodium chloride; waterHCID 57417360—
생성물2-Cyclopropyl-7-fluoro-6-formyl-5-methyl-1,3-benzoxazole-4-carbonitrileHCID 8609751186%

반응 단계

2-Cyclopropyl-7-fluoro-5-methyl-6-vinyl-1,3-benzoxazole-4-(carbonitrile (I-180) (500 mg, 2.06 mmol) was dissolved in 1,4-dioxane (7.5 ml) and water (2.5 ml), then at room temperature, 2,6-lutidine (481 μl, 4.13 mmol), a catalytic amount of osmium tetroxide and sodium metaperiodate (1.766 g, 8.26 mmol) were added. After stirring at the same temperature for 13 hours, sodium sulfite (purity 90%, 1.61 g, 12.38 mmol) and water (5 ml) were added. The solution was fractionated with ethyl acetate and saturated brine. The aqueous layer was further extracted twice with ethyl acetate. The organic layers were combined, washed with saturated brine, and dried over anhydrous sodium sulfate. The insoluble matter was separated by filtration, the solvent was evaporated away under reduced pressure, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, hexane:ethyl acetate=6:1) to obtain the entitled compound (435 mg, 86%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5c3ed14dd65e4ffbb63d2e8cd43f4d2e
출처 메모uspto-grants-2010_06