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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1500274생성일: 2026년 10월 27일

Methanesulfonyl chloride → 2,2-dichloro-1-((4S,5R)-5-(4-(6-(chloromethyl)pyridin-3-yl)phenyl)-4 (fluoromethyl)-2,2-dimethyloxazolidin-3-yl)ethanone

https://huagongshe.com/reaction/1500274

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물DiisopropylethylamineHCID 81531—
반응물2,2-dichloro-1-((4S,5R)-4-(fluoromethyl)-5-(4-(6-(hydroxymethyl)pyridin-3-yl)phenyl)-2,2-dimethyloxazolidin-3-yl)ethanoneHCID 86695406—
용매DichloromethaneHCID 6344—
생성물2,2-dichloro-1-((4S,5R)-5-(4-(6-(chloromethyl)pyridin-3-yl)phenyl)-4 (fluoromethyl)-2,2-dimethyloxazolidin-3-yl)ethanoneHCID 8671316497.5%

반응 단계

To a cooled (ice-water) solution of the product of step 1 (800 mg, 1.87 mmol) and DIPEA (0.675 mL, 3.75 mmol) in DCM (10 mL) is slowly added methanesulfonyl chloride (0.150 mL, 1.87 mmol). The reaction mixture is stirred at room temperature for 6 hours. The reaction is diluted with DCM (10 mL), washed with water (2×10 mL) dried over Na2SO4 and concentrated under reduced pressure to give the title compound (813 mg): LCMS m/z (Cl): 445 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206126B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-63de992dc7ad49eea645a79efe833794
출처 메모uspto-grants-2015_12