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HRID 1614532作成日:2026年10月27日

Amantadine → N-(Adamantan-1-yl)prop-2-enimidic acid

https://huagongshe.com/reaction/1614532

反応式

関与物質

役割名称HCID仕込み量
反応物AmantadineHCID 2130—
反応物TriethylamineHCID 8471—
反応物Acryloyl chlorideHCID 13140—
溶媒Diethyl EtherHCID 3283—
生成物N-(Adamantan-1-yl)prop-2-enimidic acidHCID 284637—

反応手順

A solution of acryloyl chloride (4.05 ml, 0.05 mole) in ethyl ether (25 ml) was added to a cold (+5° C.) solution of 1-adamantaneamine (7.65 g, 0.05 mole) and triethylamine (15.3 ml, 0.11 mole) in ethyl ether (300 ml) and the solution stirred for 72 hours at room temperature. The solvent was removed on a rotary evaporator. The residue was dissoled in ethyl acetate (100 ml), washed with 10 percent hydrochloric acid (100 ml) and water (50 ml), dried over sodium sulfate, filtered and the solvent removed in vacuo leaving an oily solid which was crystallized from methanol-ethyl acetate-hexane. The structure was confirmed by NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05198435
出典データセットuspto-grants-1993_03
ORD IDord-7ad86533a3154410807414295786aac6
出典メモuspto-grants-1993_03