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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167490생성일: 2026년 10월 26일

Sodium Bicarbonate → (5R)-3-(3-Fluoro-4-(4-methylimidazol-1-yl)phenyl)-5-hydroxymethyloxazolidin-2-one

https://huagongshe.com/reaction/1167490

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물(2R)-Oxiran-2-ylmethyl butanoateHCID 2724536—
반응물5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzeneHCID 21876672—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
용매2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
생성물(5R)-3-(3-Fluoro-4-(4-methylimidazol-1-yl)phenyl)-5-hydroxymethyloxazolidin-2-oneHCID 2135656133.7%

반응 단계

5-Benzyloxycarbonylamino-2-(4-methyl-imidazol-1-yl)fluorobenzene (54 g, 0.166 M) was dissolved in a mixture of dry tetrahydrofuran (600 ml) and 1,3-dimethyl-2,4,5,6-tetrahydro-2(1H)-pyrimidinone (100 ml) under nitrogen, cooled to −70°, and treated with a solution of n-butyllithium (1.6 M in isohexane, 114 ml), over 30 minutes. After stirring for 30 minutes at −70°, a solution of (R)-glycidylbutyrate (26.35 g, 0.183 M) in dry tetrahydrofuran (50 ml) was added over 15 minutes. Stirring was continued for 16 hours allowing the temperature to rise to ambient. The mixturc was treated with aqueous sodium bicarbonate (5%, 500 ml) and EtOAc (800 ml), and undissolved solid was removed and washed well with diethyl ether to give title product (16.3 g). The aqueous layer was further extracted with EtOAc (2×750 ml), the combined extracts dried (magnesium sulfate) and evaporated, and the residue triturated with diethyl ether. The resulting solid was recrystallisd from ethanol to give more product (10.9 g). MS (ESP): 292 (MH+) for C14H14FN3O3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06617339B1
출처 데이터셋uspto-grants-2003_09
ORD IDord-b64bbd1ddc174f42ab1454e99973db31
출처 메모uspto-grants-2003_09