関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | 2-Pyridinemethanamine | HCID 19509 | — |
| 反応物 | Benzoyl chloride, 4-(tetradecyloxy)- | HCID 9998158 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(2-Pyridinylmethyl)-4-(tetradecyloxy)benzamide | HCID 10093859 | 62.8% |
反応手順
To a 0° C. solution of 0.674 g 2-(aminomethyl)pyridine, 20 ml methylene chloride and 1.83 ml pyridine is added, dropwise over 20 minutes, 2.0 g of product from Example 3 dissolved in 25 ml of methylene chloride. The reaction is stirred at 0° C. for 2 hours followed by stirring at room temperature for 17 hours. The reaction mixture is partitioned between chloroform and saturated sodium bicarbonate, washed with water and saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by column chromatography (silica gel:75% ethyl acetate/hexane) to give 1.51 g of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05208247 |
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| 出典データセット | uspto-grants-1993_05 |
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| ORD ID | ord-0e0c972d4a26450c9db43ea2b4fff5c1 |
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| 出典メモ | uspto-grants-1993_05 |
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