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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1031542생성일: 2026년 10월 27일

Potassium Iodide → 1-{3-[4-(2-Methoxyphenyl)piperazin-1-yl]propyl}-4-(2,3,4,5,6-pentafluorophenoxy)piperidine

https://huagongshe.com/reaction/1031542

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물1-(3-Chloropropyl)-4-(2-methoxyphenyl)piperazineHCID 622669—
반응물4-(2,3,4,5,6-Pentafluorophenoxy)piperidineHCID 14837040—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1-{3-[4-(2-Methoxyphenyl)piperazin-1-yl]propyl}-4-(2,3,4,5,6-pentafluorophenoxy)piperidineHCID 1483705651.4%

반응 조건

온도75 °C

반응 단계

A mixture of 10 g of potassium carbonate, 0.18 g of potassium iodide, 4.0 g of 4-(2,3,4,5,6-pentafluorophenoxy)piperidine and 50 ml of dimethylformamide was treated with a solution of 4.56 g of 1-(3-chloropropyl)-4-(2-methoxyphenyl)piperazine in 25 ml dimethylformamide and stirred for seven hours at 75° C. After cooling to room temperature, the reaction mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water followed by a saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, evaporation afforded a residue which was purified by means of high pressure liquid chromatography (silica gel; elution with 7.5% methanol/dichloromethane). Evaporation of the appropriate fractions afforded 3.84 g of 1-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl}-4-(2,3,4,5,6-pentafluorophenoxy)piperidine as an oil. The oil was dissolved in isopropanol and acidified to pH 1 with etheral hydrogen chloride to precipitate the corresponding dihydrochloride salt. Recrystallization from isopropanol afforded 3.34 g (44.6%) of 1-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl}-4-(2,3,4,5,6-pentaflurophenoxy)piperidine hydrochloride, m.p. 261°-263° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04954511
출처 데이터셋uspto-grants-1990_09
ORD IDord-927e39ecbc0347a7bcdb9794868a2649
출처 메모uspto-grants-1990_09