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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1060976생성일: 2026년 10월 25일

Eperezolid → (S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxide

https://huagongshe.com/reaction/1060976

반응식

참여 물질

역할이름HCID투입량
반응물EperezolidHCID 73214—
반응물3-Hydroperoxyphthalic acidHCID 19809706—
용매MethanolHCID 887—
생성물(S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxideHCID 86584035—

반응 조건

온도25 °C

반응 단계

(S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]-phenyl]-2-oxo-5-oxazolidinyl]methyl]-acetamide (VIII-A, R1=COCH3, R2=H, X1=F, X2=H) (11.8 g) is dissolved in 200 mL of methanol. Monoperoxyphthalic acid, magnesium salt hexahydrate (80% pure, 18.5 g) is added and the resulting suspension is stirred at 25° C. for two hours. The reaction is filtered and the filtrate is concentrated to afford a white solid. This solid is chromatographed on silica gel using 20% methanol in chloroform as eluent to afford the N-oxide. Lyophilization of this material affords the purified product as a hydrate (9.5 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06525193B2
출처 데이터셋uspto-grants-2003_02
ORD IDord-c5fd4ac6777743028848d6cd9c0a3c34
출처 메모uspto-grants-2003_02