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HRID 728428作成日:2026年10月26日

Triethylamine → 3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane

https://huagongshe.com/reaction/728428

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Chlorobutane-1-sulphonyl chlorideHCID 74212—
反応物2-Methoxy-3-octadecylcarbamoyloxypropylamineHCID 14992262—
溶媒DichloromethaneHCID 6344—
生成物3-(4-Chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropaneHCID 1483503177%

反応手順

To a solution of 1.2 g (3 mM) of 2-methoxy-3-octadecylcarbamoyloxypropylamine IVa1 in 24 ml of dichloromethane and 0.5 ml (3.6 mM) of triethylamine is added 0.75 g (3.93 mM) of 4-chlorobutanesulfonyl chloride with ice-cooling and the mixture is stirred at room temperature overnight. The product is isolated with dichloromethane extraction and dichloromethane layer is washed with saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and evaporated. The residue is purified by the column chromatography on silica gel with a n-hexane-ethyl acetate (3:2) mixture as an eluent. The product is recrystallized from dichloromethane-n-hexane to give 1.28 g (2.305 mM) of 3-(4-chlorobutylsulfonylamino)-2-methoxy-1-octadecylcarbamoyloxypropane IIIa5 as colorless crystals in 77% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05047540
出典データセットuspto-grants-1991_09
ORD IDord-3eaddd452a6a4961beaa3b84ccbf49b8
出典メモuspto-grants-1991_09