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HRID 242093作成日:2026年10月27日

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

https://huagongshe.com/reaction/242093

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—
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US08653100B2
出典データセットuspto-grants-2014_02
ORD IDord-1ece4bdf720c4e0983629188cef4e8cb
出典メモuspto-grants-2014_02