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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-(3-Phenylpropyl)piperidine | HCID 87678 | — |
| 反応物 | 3-(3-Chloropropyl)-6-fluorobenzo[d]isoxazole | HCID 10910880 | — |
| 触媒 | Potassium Iodide | HCID 4875 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-[3-(6-Fluoro-1,2-benzisoxazol-3-yl)propyl]-4-(3-phenylpropyl)piperidine hydrochloride | HCID 13319854 | 75.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04591586 |
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| 出典データセット | uspto-grants-1986_05 |
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| ORD ID | ord-5e59c6e8b46a4e1daaf822fe8670eaec |
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| 出典メモ | uspto-grants-1986_05 |
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