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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64875생성일: 2026년 10월 24일

1-(3-(Trifluoromethyl)phenyl)piperazine → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochloride

https://huagongshe.com/ko/reaction/64875

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-(Trifluoromethyl)phenyl)piperazineHCID 4296—
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
용매DimethylformamideHCID 6228—
생성물1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-trifluoromethylphenyl)piperazine hydrochlorideHCID 1352073735.8%

반응 단계

A mixture of 6.5 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 5.8 g of N-(α,α,α-trifluoro-m-tolyl)piperazine, 7.0 g of potassium carbonate and a few crystals potassium iodide in 80 ml of dimethylformamide was stirred at 70°-75° C. for seven hrs. The reaction mixture was cooled, filtered and concentrated to an oil, which was stirred with water and extracted with ether-ethyl acetate. The organic extracts were washed with water (2×), saturated sodium chloride solution, and dried over anhydrous magnesium sulfate. The mixture was filtered and concentrated to an oil, which was converted to a salt by treatment with ethereal hydrogen chloride. The salt was recrystallized from ethyl acetate/methanol to give 4 g (35%) of product mp, 208°-209° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04610988
출처 데이터셋uspto-grants-1986_09
ORD IDord-c2676640fd80454395df9609f6d257ce
출처 메모uspto-grants-1986_09