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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456784생성일: 2026년 10월 24일

Triethylamine → Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl ester

https://huagongshe.com/ko/reaction/456784

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Compound 3HCID 20788885—
용매DichloromethaneHCID 6344—
용매Sodium BicarbonateHCID 516892—
생성물Methanesulfonic acid (5R)-3-(3-fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl esterHCID 2362470598.4%

반응 단계

(5R)-3-(3-Fluoro-4-iodophenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-one (Intermediate 3, 25.0 g, 74.2 mmol) was stirred in dichloromethane (250 ml) at 0° C. Triethylamine (10.5 g, 104 mmol) was added followed by methanesulfonyl chloride (11.2 g, 89.0 nmmol) and the reaction was stirred overnight, slowly warming to room temperature. The yellow solution was diluted with sodium bicarbonate and the compound was extracted using dichloromethane (3×250 ml). The organic layer was dried (magnesium sulfate), filtered and concentrated to give the desired product as a light yellow solid (30.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07186738B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-322d6d8ce893421388ace316223beabc
출처 메모uspto-grants-2007_03