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HRID 245314생성일: 2026년 10월 26일

Ammonium Chloride → (S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one

https://huagongshe.com/reaction/245314

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Carbamic acid, N-(3-fluoro-4-(4-morpholinyl)phenyl)-, phenylmethyl esterHCID 5306150—
반응물2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
반응물(S)-1-chloro-3-(dibenzylamino)propan-2-olHCID 49765557—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(S)-5-((dibenzylamino)methyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-oneHCID 1121366882%

반응 단계

N-carbobenzoxy-3-fluoro-4-morpholinylaniline (0.33 g, 1 mmol) and lithium tert-butoxide (0.19 g, 2.4 mmol) were added under nitrogen atmosphere to 10 mL of tetrahydrofuran and the mixture was stirred at room temperature for 2 hours. (S)-1-chloro-3-(dibenzylamino)propan-2-ol (0.32 g, 1.1 mmol) was added and then reaction mixture was heated to 60° C. and stirred for 8 hours. Saturated ammonium chloride solution, and ethyl acetate were added to separate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, filtered, and the solvent was evaporated to provide 0.39 g of off-white solid in 82% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658789B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-cb1f6d8b19e5487e8bc7983c9d838c8d
출처 메모uspto-grants-2014_02