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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1804242생성일: 2026년 10월 27일

Hydrochloric Acid → 3-{4-[4-(2,4-Dimethylphenyl)-[1,4]diazepane-1-carbonyl]phenyl}oxazolidin-2-one

https://huagongshe.com/reaction/1804242

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-MethylmorpholineHCID 7972—
반응물Sodium HydroxideHCID 14798—
반응물Ethyl p-(2-oxo-1,3-oxazolidin-3-yl)benzoateHCID 616604—
반응물4-(4,6-Dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrateHCID 23149411—
반응물1-(2,4-Dimethylphenyl)-[1,4]diazepane hydrochlorideHCID 67380883—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물3-{4-[4-(2,4-Dimethylphenyl)-[1,4]diazepane-1-carbonyl]phenyl}oxazolidin-2-oneHCID 4619022910.6%

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온도50 °C

반응 단계

To ethyl 4-(2-oxooxazolidin-3-yl)benzoate (0.235 g) described in Preparation Example 12 were added 1N aqueous sodium hydroxide solution (1.3 mL) and ethanol (5 mL), and the mixture was stirred at 50° C. 1N hydrochloric acid (1.3 mL) was added, 1-(2,4-dimethylphenyl)-[1,4]diazepane hydrochloride (0.241 g) described in Preparation Example 88, 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (0.277 g) and N-methylmorpholine (0.13 mL) were added, and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (41.8 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354401B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-045a7db7c6eb4aedb1222503887af23c
출처 메모uspto-grants-2013_01