戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 3761作成日:2026年10月25日

Water → N-(1-Azabicyclo[2.2.2]oct-3-yl)-2,4-dimethoxybenzamide hydrochloride

https://huagongshe.com/reaction/3761

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium CarbonateHCID 10340—
反応物Quinuclidine, 3-amino-, dihydrochlorideHCID 197853—
反応物2,4-Dimethoxybenzoyl chlorideHCID 2734719—
溶媒ChloroformHCID 6212—
生成物N-(1-Azabicyclo[2.2.2]oct-3-yl)-2,4-dimethoxybenzamide hydrochlorideHCID 1327233023.7%

反応手順

A mixture of 3-aminoquinuclidine dihydrochloride, 6.95 g, (0.349), 2,4-dimethoxybenzoyl chloride, 700 g, (0.0349 mole), anhydrous sodium carbonate, 36.99 g, (0.349 mole), 175 ml water, and 175 ml chloroform was stirred rapidly to achieve good mixing of the 2 layers for 20 hrs. The chloroform layer was then separated, washed with water, dried over anhydrous magnesium sulfate, and concentrated to an impure oil. The oil was triturated twice with 20 ml portions of petroleum ether to remove some impurities. The oil was then dissolved in diethyl ether and filtered to remove a small amount of insoluble material. The filtrate was treated with ethereal hydrogen chloride and the resulting salt collected to yield 2.70 g (23.7% yield) white solid. The salt was recrystallized from ethanol-isopropyl ether. Further recrystallization from methanol-ethyl ether yielded a white solid, m.p. 211°-212° C. The NMR analysis was satisfactory.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722834
出典データセットuspto-grants-1988_02
ORD IDord-217b10af343044bfa5761f4da10eaeb8
出典メモuspto-grants-1988_02