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HRID 280885作成日:2026年10月26日

Potassium Carbonate → 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-phenylpropyl)piperidine hydrochloride

https://huagongshe.com/reaction/280885

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-(3-Phenylpropyl)piperidineHCID 87678—
反応物3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazoleHCID 10910880—
触媒Potassium IodideHCID 4875—
溶媒DimethylformamideHCID 6228—
生成物1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-phenylpropyl)piperidine hydrochlorideHCID 1331985475.3%

反応条件

温度90 °C

反応手順

To 40 ml of dimethylformamide was added 4.06 g of 4-(3-phenylpropyl)piperidine, 3.4 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 extract was washed with water (2x), saturated sodium chloride solution and dried over anhydrous magnesium sulfate. After filtering, the solution was acidified to pH 1 with ethereal hydrogen chloride. The resultant precipitate was collected and dried to give 5.0 g (60%) of product, mp 95° C. Recrystallization from ethyl acetate/methanol (5:1) gave the analytical sample, mp 136°-137° 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-5e59c6e8b46a4e1daaf822fe8670eaec
出典メモuspto-grants-1986_05