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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-methyl-2-(tributylstannyl)-1H-pyrrole | HCID 2769397 | — |
| 반응물 | 2-Chloro-7-fluoro-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 51041429 | — |
| 반응물 | 2,6-Di-t-butylcresol | HCID 66637192 | — |
| 촉매 | HCID 178418476 | HCID 178418476 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 7-fluoro-5-methyl-2-(1-methyl-1H-pyrrol-2-yl)-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737166B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-2d23f605678b474eaf1831fc88ee31f9 |
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| 출처 메모 | uspto-grants-2010_06 |
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