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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 723885생성일: 2026년 10월 26일

Phosgene → methyl (5R)-3-[4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenyl]-2-oxo-5-oxazolidinecarboxylate

https://huagongshe.com/reaction/723885

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물TriethylamineHCID 8471—
반응물methyl (2R)-3-{[4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenyl]amino}-2-hydroxypropanoateHCID 86610079—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물methyl (5R)-3-[4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenyl]-2-oxo-5-oxazolidinecarboxylateHCID 6848931083%

반응 단계

A solution of methyl (2R)-3-{[4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenyl]amino}-2-hydroxypropanoate (Step 1, 1.02 g, 2.90 mmol) in CH2Cl2 (25 mL) and triethylamine (1.0 g, 1.5 mL, 10.5 mmol) is cooled to 0° C. and treated with phosgene (1.94 mL of a 20% solution in toluene, 3.6 mmol). After stirring at room temperature for one hour, the reaction mixture is diluted with CH2Cl2 and washed with dilute NaHCO3, saline, and dried (MgSO4), filtered and concentrated. Chromatography on silica gel (10% acetonitrile-dichloromethane) provides the title compound (0.91 g, 83%), MS (m/z): [M+H]+=391; 1H NMR (300 MHz, CDCl3): δ 3.16–3.20 (m, 4H), 3.64 (m, 4H), 3.88 (s, 3H), 4.06–4.11 (m, 1H), 4.23 (t, 1H), 5.06–5.11 (m, 1H), 7.16 (d, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141588B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-e3924cc9ad8740028aa2bcc6e3b1d94d
출처 메모uspto-grants-2006_11