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HRID 1071985作成日:2026年10月25日

O-Methyltyramine → N-(2-p-methoxyphenylethyl)-p-fluorophenylpropionamide

https://huagongshe.com/reaction/1071985

反応式

関与物質

役割名称HCID仕込み量
反応物O-MethyltyramineHCID 4657—
反応物2-(4-Fluorophenyl)propionic acidHCID 2723915—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒DichloromethaneHCID 6344—
生成物N-(2-p-methoxyphenylethyl)-p-fluorophenylpropionamideHCID 86595127—

反応手順

To a stirred mixture of p-methoxyphenethyl amine (3.28 g, 21.7 mmol), p-fluorophenyl propionic acid (3.31 g, 19.7 mmol), and 150 ml anhydrous dichloromethane was added 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (4.16 g, 21.7 mmol). The mixture was stirred at ambient temperature for 40 hours and then washed with 1N sodium hydroxide, 1N hydrochloric acid, and saturated sodium chloride, dried, filtered and evaporated to a green solid (5.41 g, 91%). 1H NMR (CDCl3) δ 7.18 (m, 2H); 6.98 (m, 4 H); 6.81 (d, 2 H); 5.32 (br s, 1 H); 3.79 (s, 3 H); 3.44 (q, 2 H); 2.90 (t, 2 H); 2.68 (t, 2 H); 2.39 (t, 2 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06908931B2
出典データセットuspto-grants-2005_06
ORD IDord-82a3d6481c9940d29cbe58b48fd548d2
出典メモuspto-grants-2005_06