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HRID 245321作成日:2026年10月25日

Nitrogen → Linezolid

https://huagongshe.com/reaction/245321

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Acetic AnhydrideHCID 7918—
反応物TriethylamineHCID 8471—
反応物(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-oneHCID 11213668—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒AcetoneHCID 180—
生成物LinezolidHCID 44140175.6%

反応手順

(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one (0.95 g, 2 mmol) and 0.1 g 10 wt % Pd—C were added to 20 mL acetone and the air was replaced with N2. The reaction went on under 5 Mpa hydrogen at room temperature for 5 hours. After filtered, acetic anhydrid (0.24 g, 2.4 mmol) and triethylamine (2.0 g, 20 mmol) were added and reacted for 2 hours at room temperature. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered, most part of the solvent was evaporated, frozen crystallized and filtered to provide the crude product. The crude product was recrystallized with ethyl acetate to provide 0.51 g of linezolid in 75% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658789B2
出典データセットuspto-grants-2014_02
ORD IDord-7d088d57876841848e04e42cad2c39d7
出典メモuspto-grants-2014_02