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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 583568생성일: 2026년 10월 26일

Iodine chloride → (S)-N-[3-(3-Fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide

https://huagongshe.com/reaction/583568

반응식

참여 물질

역할이름HCID투입량
반응물Iodine chlorideHCID 24640—
반응물(S)-N-[[3-(3-Fluorophenyl)-2-oxo-5-oxazolidinyl]methyl]acetamideHCID 11345751—
용매Acetic AcidHCID 176—
용매Diethyl EtherHCID 3283—
용매Trifluoroacetic acidHCID 6422—
생성물(S)-N-[3-(3-Fluoro-4-iodo-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-acetamideHCID 11222662—

반응 단계

(S)-N-[[3-(3-fluorophenyl)-2-oxo-5-oxazolidinyl]methyl]- acetamide (PREPARATION 17, 0.280 g, 1.11 mmol) is dissolved in a mixture of acetic acid (20 ml) and trifluoroacetic acid (5 ml) and then treated with iodine monochloride (2.343 g, 14.43 mmol) at 20-25°. The mixture is stirred at 20-25° under nitrogen. After about 24 hr the reaction mixture is diluted with ether and the solids collected under reduced pressure through a medium-porosity sintered glass filter, washing with ether. The crude solids are dissolved in hot chloroform (a little methanol is added), transferred to a separatory funnel, and washed with saturated aqueous sodium bicarbonate, 20% aqueous sodium thiosulfate and brine. The organic phase is separated, dried over sodium sulfate, filtered and concentrated under reduced pressure to give the title compound, mp 185.5-186.5°; [α]25D -37.6° (c 1.0, DMF).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05929248
출처 데이터셋uspto-grants-1999_07
ORD IDord-f725227dec0845f084ddacb0005cc789
출처 메모uspto-grants-1999_07