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HRID 1609209作成日:2026年10月25日

Ammonia → N-(1-benzyloxycarbonylcyclopentyl)-N-(2'-cyanobiphenyl-4-ylmethyl)-N-pentanoyl-amine

https://huagongshe.com/reaction/1609209

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Valeryl chlorideHCID 61186—
反応物DiisopropylethylamineHCID 81531—
反応物N-(1-benzyloxycarbonylcyclopentyl)-N-(2'-cyano-biphenyl-4-ylmethyl)-amine hydrochlorideHCID 20083511—
溶媒Ethyl AcetateHCID 8857—
生成物N-(1-benzyloxycarbonylcyclopentyl)-N-(2'-cyanobiphenyl-4-ylmethyl)-N-pentanoyl-amineHCID 20083535—

反応手順

A solution of 2.9 g (6.5 mmol) of N-(1-benzyloxycarbonylcyclopentyl)-N-(2'-cyano-biphenyl-4-ylmethyl)-amine hydrochloride and 4.4 ml (26 mmol) of Hunig base in 50 ml of ethyl acetate is treated with 1.1 g (9 mmol) of pentanoyl chloride, and the mixture is stirred for 15 hours at 25°-30°. After the addition of a further 0.5 g of pentanoyl chloride the mixture is stirred for a further 8 hours. The reaction mixture is then treated with 10 ml of aqueous ammonia solution (5%) and stirred for 0,5 hours. The ethyl acetate phase is separated, washed in succession with 2 N-hydrochloric acid, water and sodium hydrogencarbonate solution, dried and evaporated. The N-(1-benzyloxycarbonylcyclopentyl)-N-(2'-cyanobiphenyl-4-ylmethyl)-N-pentanoyl-amine is thus obtained in the form of a brown oil [Rf : 0.53 (system B7)], which is used for further reactions in crude form.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05399578
出典データセットuspto-grants-1995_03
ORD IDord-45dff45efdab4e3eb906fc6aaaaed7c2
出典メモuspto-grants-1995_03