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HRID 480186作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物4-Chloro-2-nitrophenolHCID 6980—
反応物Potassium CarbonateHCID 11430—
反応物rel-Methyl 5-chloro-2-[2-[(2R,5S)-4-[(4-fluorophenyl)methyl]-2,5-dimethyl-1-piperazinyl]-2-oxoethoxy]benzoateHCID 11487716—
溶媒WaterHCID 962—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物2-(4-Chloro-2-nitro-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 4443152593%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06649611B2
出典データセットuspto-grants-2003_11
ORD IDord-1089e2043a264e1895e01c690b11c3aa
出典メモuspto-grants-2003_11