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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17435생성일: 2026년 10월 24일

1-methyl-2-(tributylstannyl)-1H-pyrrole → 7-fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile

https://huagongshe.com/ko/reaction/17435

반응식

참여 물질

역할이름HCID투입량
반응물1-methyl-2-(tributylstannyl)-1H-pyrroleHCID 2769397—
반응물2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 51041429—
반응물2,6-Di-t-butylcresolHCID 66637192—
촉매HCID 178418476HCID 178418476—
용매TolueneHCID 1140—
생성물7-fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrileHCID 51039965—

반응 단계

Tributylstannyl-1-methylpyrrole (389 mg, 1.05 mmol), bis(triphenylphosphine)palladium(II) dichloride (49 mg, 0.07 mmol), and a catalytic amount of 2,6-di-tert-butylcresol (2 mg) were added to a toluene (20 ml) solution of 2-chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-cabonitrile (I-130) (200 mg, 0.70 mol), followed by stirring under heat under nitrogen atmosphere for 3 hours. After cooling, the reaction liquid was filtered, and the solvent of the filtrate was evaporate away under reduced pressure. The resulting residue was subjected to silica gel column chromatography, and eluted with a mixed solvent of n-hexane/ethyl acetate (9:1, v/v→5:1, v/v) to obtain a main product. After washing with isopropyl ether, the entitled compound (50 mg, 22%) was collected by filtration as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737166B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2d23f605678b474eaf1831fc88ee31f9
출처 메모uspto-grants-2010_06