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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480186생성일: 2026년 10월 26일

Potassium Iodide → 2-(4-Chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/480186

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물4-Chloro-2-nitrophenolHCID 6980—
반응물Potassium CarbonateHCID 11430—
반응물rel-Methyl 5-chloro-2-[2-[(2R,5S)-4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]-2-oxoethoxy]benzoateHCID 11487716—
용매WaterHCID 962—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-(4-Chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 4443152593%

반응 단계

To a solution of (2R, 5S)-5-chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzoic acid methyl ester (1.0 g, 3.35 mmol) in butanone (35 ml) was added 2-nitro-4-chlorophenol (0.639 g, 3.69 mmol), potassium carbonate (0.925 g, 6.7 mmol) and potassium iodide (0.556 g, 3.35 mmol). The reaction mixture was heated at reflux overnight. The reaction mixture was then cooled, diluted with water and extracted with ethyl acetate. The combined organics were dried over magnesium sulfate, filtered and concentrated to give an orange oil. Chromatography on silica gel gave the title compound (1.35 g, 93% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649611B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-1089e2043a264e1895e01c690b11c3aa
출처 메모uspto-grants-2003_11