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HRID 651213作成日:2026年10月24日

Linezolid → (S)-N-[[3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide N-oxide

https://huagongshe.com/ja/reaction/651213

反応式

関与物質

役割名称HCID仕込み量
反応物LinezolidHCID 441401—
反応物3-Hydroperoxyphthalic acidHCID 19809706—
溶媒MethanolHCID 887—
生成物(S)-N-[[3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide N-oxideHCID 86757261—

反応条件

温度25 °C

反応手順

(S)-N-[[3-[3-Fluoro-4-(4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]-acetamide (III-A, R1=COCH8, X1=F, X2=H) (12.5 g) is suspended in 200 mL of methanol. Monoperoxyphthalic acid, magnesium salt hexahydrate (80% pure, 11.5 g) is added and the resulting suspension is stirred at 25° C. for two hours. The reaction mixture is filtered and the filtrate is concentrated to afford a light-yellow solid. This material is chromatographed on silica gel using 10% methanol (saturated with ammonia) in chloroform as eluent to afford 8.75 g of the N-oxide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06277985B1
出典データセットuspto-grants-2001_08
ORD IDord-449ccaf3ce3942d782a26ff5b0f04886
出典メモuspto-grants-2001_08