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HRID 323797作成日:2026年10月27日

Diethyl Ether → 1-[4-(4-Fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl ester

https://huagongshe.com/reaction/323797

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物TriethylamineHCID 8471—
反応物Benzyl 1-aminocyclopentanecarboxylate 4-methylbenzenesulfonateHCID 254983—
反応物4-(4-Fluorophenoxy)benzenesulphonyl chlorideHCID 2782757—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物1-[4-(4-Fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl esterHCID 11005171—

反応手順

To a solution of 1-aminocyclopentanecarboxylic acid benzyl ester p-toluenesulfonic acid salt (200 grams, 0.51 mole) and triethylamine (177 mL, 1.27 mole) in water (1 L) and 1,2-dimethoxyethane (1 L) was added 4-(4-fluorophenoxy)benzenesulfonyl-chloride (161 grams, 0.56 moles). The mixture was stirred at room temperature for 16 hours and then most of the solvent was removed by evaporation under vacuum. The mixture was diluted with ethyl acetate and was washed successively with dilute hydrochloric acid solution, water, and brine. The solution was dried over magnesium sulfate and concentrated to leave a brown solid. Trituration with diethyl ether to afforded 1-[4-(4-fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl ester as a tan solid, 167 grams (70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06214872B1
出典データセットuspto-grants-2001_04
ORD IDord-394ef33598854287a8a09a224efd90bf
出典メモuspto-grants-2001_04