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HRID 1060976作成日:2026年10月26日
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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Eperezolid | HCID 73214 | — |
| 反応物 | 3-Hydroperoxyphthalic acid | HCID 19809706 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxide | HCID 86584035 | — |
反応手順
(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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06525193B2 |
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| 出典データセット | uspto-grants-2003_02 |
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| ORD ID | ord-c5fd4ac6777743028848d6cd9c0a3c34 |
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| 出典メモ | uspto-grants-2003_02 |
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