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HRID 247914作成日:2026年10月27日

Pyridine → N-(2-Pyridinylmethyl)-4-(tetradecyloxy)benzamide

https://huagongshe.com/reaction/247914

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-PyridinemethanamineHCID 19509—
反応物Benzoyl chloride, 4-(tetradecyloxy)-HCID 9998158—
溶媒DichloromethaneHCID 6344—
生成物N-(2-Pyridinylmethyl)-4-(tetradecyloxy)benzamideHCID 1009385962.8%

反応条件

温度0 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05208247
出典データセットuspto-grants-1993_05
ORD IDord-0e0c972d4a26450c9db43ea2b4fff5c1
出典メモuspto-grants-1993_05