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HRID 11486作成日:2026年10月24日

Methanol → 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide

https://huagongshe.com/ja/reaction/11486

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TriethylamineHCID 8471—
反応物Oxydiacetyl dichlorideHCID 88769—
反応物2-(1Adamantyl)-n-pentylethylamine hydrochlorideHCID 49831680—
溶媒DichloromethaneHCID 6344—
生成物2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamideHCID 5748127360%

反応手順

2-(1-Adamantyl)-N-pentylethylamine hydrochloride (Intermediate No. 1-1) (0.50 g, 1.7 mmol) was added to a solution of diglycolyl chloride (0.31 ml, 2.6 mmol) and triethylamine (0.70 ml, 5.1 mmol) in anhydrous dichloromethane (6 ml) under ice-cooling, and the mixture was stirred at room temperature overnight. Methanol (5 ml) was added to the reaction mixture, and the whole was stirred for three hours. The solvent was evaporated under reduced pressure, the residue was distributed with ethyl acetate and water (15 ml respectively), and the organic layer was washed with a saturated aqueous sodium chloride solution (5 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the resulting residue was purified by silica gel column chromatography to give 0.39 g (60%) of 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide as an oily matter.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098226B2
出典データセットuspto-grants-2006_08
ORD IDord-255a07025eca44d1b3ec05d62aa736eb
出典メモuspto-grants-2006_08