戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2399700作成日:2026年10月26日

Triethylamine → N-(1,1-Diethyl-prop-2-ynyl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butyramide

https://huagongshe.com/reaction/2399700

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物3-Ethylpent-1-yn-3-amineHCID 76710—
反応物4-[4-(2-Methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acidHCID 9863428—
反応物N,N-bis(2-oxo-3oxazolidinyl)phosphoramidic chlorideHCID 19975454—
溶媒DichloromethaneHCID 6344—
生成物N-(1,1-Diethyl-prop-2-ynyl)-4-[4-(2-methoxy-phenyl)-piperazin-1-yl]-2-phenyl-butyramideHCID 1529637426.8%

反応手順

A mixture of 4-[4-(2-methoxyphenyl)piperazin-1-yl]-2-phenylbutanoic acid (1.772 g, 5 mmole), triethylamine (1.518 g, 15 mmole), and N,N-bis(2-oxo-3-oxazolidinyl)phosphoramidic chloride (1.527 g, 6 mmole) was stirred in methylene chloride (80 mL) under exclusion of moisture at ambient temperature for 30 minutes, after which 1,1-diethylpropargylamine (0.668 g, 6 mmole) was added at once at 0° C. The reaction mixture was stirred at room temperature overnight, washed with water (2×100 mL), dried over magnesium sulfate, filtered, and evaporated to dryness in vacuo. Chromatography on silica gel with methanol/chloroform as eluant, followed by trituration from diethyl ether with addition of ethanolic hydrochloric acid gave 0.6 g of the title compound as the trihydrochloride hemihydrate, m.p. 110°-12° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05451584
出典データセットuspto-grants-1995_09
ORD IDord-cf7ea46d5e13469ab5cf8bc2154f4afc
出典メモuspto-grants-1995_09