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HRID 1850873作成日:2026年10月26日

O-Methyltyramine → 1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamide

https://huagongshe.com/reaction/1850873

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1-(p-Chlorophenyl)cyclopropanecarboxylic acidHCID 98606—
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
溶媒WaterHCID 962—
生成物1-(4-chlorophenyl)-N-[2-(4-methoxyphenyl)ethyl]cyclopropanecarboxamideHCID 60409668—

反応手順

A solution of 1-(4-chlorophenyl)cyclopropanecarboxylic acid (5.0 g, 25.3 mmol), 2-(4-methoxyphenyl)ethanamine (4.2 g, 28 mmol) and 4-N,N-Dimethylaminopyridin (3.3 g; 28 mmol) in methylenehloride (200 ml) was cooled to −10° C. N-ethyl-N′-(3-Dimethylaminopropyl)-carbodiimid hydrochloride (EDC, 5.3 g, 28 mmol) was added in several portions and the resulting mixture stirred overnight. The reaction mixture was poured into water and consecutively extracted with water, 2N NaOH and 1N HCl. Evaporation of the dried (NaSO4) extract yielded an oily residue that crystallized upon addition of n-heptan, which was used without further purification. Yield 7.0 g (21.2 mmol, 83%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08957089B2
出典データセットuspto-grants-2015_02
ORD IDord-bef0d4a902b649ad986996cdb96c4d6a
出典メモuspto-grants-2015_02