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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 480193생성일: 2026년 10월 25일

Potassium Iodide → (2R,5S)-5-Chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehyde

https://huagongshe.com/reaction/480193

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물5-Chloro-salicylaldehydeHCID 12481—
반응물2-Chloro-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanoneHCID 21973276—
용매DimethylformamideHCID 6228—
용매Sodium chloride; waterHCID 57417360—
생성물(2R,5S)-5-Chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehydeHCID 5367380785%

반응 조건

온도100 °C

반응 단계

To a solution of 2-chloro-1-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-ethanone (2.87 g, 9.6 mmol) in DMF (20 mL) was added 5-chlorosalicylaldehyde (1.65 g, 10.5 mmol), potassium carbonate (2.64 g, 19.2 mmol) and potassium iodide (1.59 g, 9.6 mmol). The resulting mixture was heated to 100° C. for 12 hours. The reaction was cooled, diluted with saturated aqueous brine and extracted with ethyl acetate (3×). The combined organics were dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo to give crude product. Purification via chromatography on silica gel (15% EtOAc/Hexanes) gave the title compound 3.40 g, 85% yield.)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06649611B2
출처 데이터셋uspto-grants-2003_11
ORD IDord-75890e2ef89f4f75a97921c7e64b3dc4
출처 메모uspto-grants-2003_11