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HRID 280896作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-Phenylpiperidine-4-carbonitrile hydrochlorideHCID 3084973—
反応物3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
触媒Potassium IodideHCID 4875—
溶媒DimethylformamideHCID 6228—
生成物4-Cyano-1-[3-(6-fluoro-1,2-benzisoxazol-3-yl)propyl]-4-phenylpiperidine hydrochlorideHCID 1331987230.4%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04591586
出典データセットuspto-grants-1986_05
ORD IDord-0b413f610e0e4919aca5324749640a11
出典メモuspto-grants-1986_05