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HRID 1059075作成日:2026年10月25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/1059075

反応式

関与物質

役割名称HCID仕込み量
反応物EperezolidHCID 73214—
反応物3-Hydroperoxyphthalic acidHCID 19809706—
溶媒MethanolHCID 887—
生成物(S)-N-[[3-[3-Fluoro-4-[4-(hydroxyacetyl)-1-piperazinyl]phenyl]-2-oxo-5-oxazolidinyl]-methyl]acetamide N-oxideHCID 86584035—

反応条件

温度25 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06518427B1
出典データセットuspto-grants-2003_02
ORD IDord-171f06a0489a408cbf774712bf98b0fb
出典メモuspto-grants-2003_02