関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-(2-Methoxyphenyl)pyrrolidine | HCID 15029963 | — |
| 反応物 | 8-(Bromomethyl)-1,4-dioxaspiro[4.5]decane | HCID 22236570 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 溶媒 | 2-Naphthylalanine | HCID 185915 | — |
| 生成物 | 1-(1.4-Dioxaspiro[4.5]dec-8-ylmethyl)-3-(2-methoxyphenyl)pyrrolidine | HCID 22236569 | — |
反応手順
1 g of 3-(2-Methoxyphenyl)pyrrolidine is dissolved in 60 ml of dioxane and 0.85 g Nal, followed by 1.2 ml of N,N-ethyldiisopropylamine and 1.5 g of 8-bromomethyl-1.4-dioxaspiro[4.5]decane, dissolved in 5 ml of dioxane, are added. The reaction mixture is stirred overnight at 80°, evaporated and the residue extracted with ethylacetate/2N Na2CO3, followed by aqueous NaCl. The combined, dried and evaporated organic phases yields an oily residue which is purified by flash chromatography on silica gel using t-butylmethylether as a solvent system providing the product as an oil. MS (EI): M+=331; NMR (DMSO): 1.1 (2H, m), 1.45 (3H, m), 1.6-1.8 (5H, m), 2.15 (1H, m), 2.25 (2H, m), 2.4 (1H, t), 2.6 (2H, m), 2.8 (1H, t), 3.6 (1H, t), 3.75 (3H, s), 3.85 (4H, s), 6.9 (2H, dd), 7.15 (1H, t), 7.3 (1H, d).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07012085B2 |
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| 出典データセット | uspto-grants-2006_03 |
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| ORD ID | ord-921c6d0112b64f239809152970731724 |
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| 出典メモ | uspto-grants-2006_03 |
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