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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245321생성일: 2026년 10월 25일

Nitrogen → Linezolid

https://huagongshe.com/reaction/245321

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Acetic AnhydrideHCID 7918—
반응물TriethylamineHCID 8471—
반응물(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-oneHCID 11213668—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매AcetoneHCID 180—
생성물LinezolidHCID 44140175.6%

반응 단계

(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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658789B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-7d088d57876841848e04e42cad2c39d7
출처 메모uspto-grants-2014_02