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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 280896생성일: 2026년 10월 24일

Potassium Carbonate → 4-Cyano-1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperidine hydrochloride

https://huagongshe.com/ko/reaction/280896

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
반응물3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
촉매Potassium IodideHCID 4875—
용매DimethylformamideHCID 6228—
생성물4-Cyano-1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperidine hydrochlorideHCID 1331987230.4%

반응 조건

온도90 °C

반응 단계

To 50 ml of dimethylformamide was added 4.4 g of 4-cyano-4-phenylpiperidine hydrochloride, 6.4 g of 3-(3-chloropropyl)-6-fluoro-1,2-benzisoxazole, 10 g of milled potassium carbonate, and 0.01 g of potassium iodide. After stirring at 90° C. for three hrs, the mixture was cooled, filtered, and the filtrate was evaporated to an oil. The oil was stirred with 100 ml of water for ten mins and then extracted with ether. The ether solution was washed with water (2x), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solvent was evaporated. The residue was filtered through a silica gel column with tetrahydrofuran. The eluant was evaporated to an oil. The oil was dissolved in ether and treated with ethereal hydrogen chloride to give 2.4 g (29%) of product, mp 235° C. (dec). Recrystallization from ethyl acetate/methanol gave the analytical sample, mp 239° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04591586
출처 데이터셋uspto-grants-1986_05
ORD IDord-0b413f610e0e4919aca5324749640a11
출처 메모uspto-grants-1986_05