Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78718생성일: 2026년 10월 24일
Bis(trifluoroacetoxy)iodobenzene → Tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(3-(2-hydroxyphenyl)isoxazol-5-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate
https://huagongshe.com/ko/reaction/78718
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bis(trifluoroacetoxy)iodobenzene | HCID 102317 | — |
| 반응물 | Tert-butyl 3-[4-[5-[bis(tert-butoxycarbonyl)amino]-6-ethynyl-pyrazin-2-yl]phenyl]sulfonylpiperidine-1-carboxylate | HCID 86682774 | — |
| 반응물 | Salicylaldoxime | HCID 135408751 | — |
| 용매 | Methanol--water (1/1) | HCID 22242641 | — |
| 생성물 | Tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(3-(2-hydroxyphenyl)isoxazol-5-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate | HCID 136387756 | 78% |
반응 단계
PIFA was added to a stirred solution of tert-butyl 3-[4-[5-[bis(tert-butoxycarbonyl)amino]-6-ethynyl-pyrazin-2-yl]phenyl]sulfonylpiperidine-1-carboxylate (150 mg,) and (E)-2-hydroxybenzaldehyde oxime in MeOH/water (0.4 mL) and the reaction mixture stirred at ambient temperature for 1.5 hours. A further portion of PIFA was added and the reaction mixture stirred at ambient temperature for a further 1.5 hours. The reaction mixture was partitioned between ethylacetate and water and the layers separated. The aqueous layer was extracted with ethylacetate (×1) and the combined organic extracts dried over MgSO4, filtered and concentrated in vacuo. The residue was purified by column chromatography (ISCO Companion, 24 g column, eluting with 0 to 50% Petroleum/Petroleum Ether, loaded in DCM) to give tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(3-(2-hydroxyphenyl)isoxazol-5-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylate as an off-white solid (142 mg, 78%). LC/MS m/z 722.1 [M−56+1]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841449B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-393fa319b5c546d5acf1eefcefdf473e |
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| 출처 메모 | uspto-grants-2014_09 |
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