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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

반응식

참여 물질

역할이름HCID투입량
반응물Bis(trifluoroacetoxy)iodobenzeneHCID 102317—
반응물Tert-butyl 3-[4-[5-[bis(tert-butoxycarbonyl)amino]-6-ethynyl-pyrazin-2-yl]phenyl]sulfonylpiperidine-1-carboxylateHCID 86682774—
반응물SalicylaldoximeHCID 135408751—
용매Methanol--water (1/1)HCID 22242641—
생성물Tert-butyl 3-((4-(5-((tert-butoxycarbonyl)amino)-6-(3-(2-hydroxyphenyl)isoxazol-5-yl)pyrazin-2-yl)phenyl)sulfonyl)piperidine-1-carboxylateHCID 13638775678%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841449B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-393fa319b5c546d5acf1eefcefdf473e
출처 메모uspto-grants-2014_09