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HRID 323801作成日:2026年10月26日

Iodoethane → 1{(2-Ethoxycarbonylethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentane carboxylic acid benzyl ester

https://huagongshe.com/reaction/323801

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物Potassium CarbonateHCID 11430—
反応物1{(2-Carboxyethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentanecarboxylic acid benzyl esterHCID 15524281—
溶媒DimethylformamideHCID 6228—
生成物1{(2-Ethoxycarbonylethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentane carboxylic acid benzyl esterHCID 1552428296.4%

反応手順

To a solution of 1{(2-carboxyethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentanecarboxylic acid benzyl ester (147 grams) in N,N-dimethyl formamide (3 L) at room temperature was added potassium carbonate (150 grams, 1.08 mole) and ethyl iodide (32.4 mL, 0.405 mole). The mixture was stirred for 16 hours at room temperature. After filtration, most of the solvent was removed under vacuum. The residue was taken up in water and acidified using 6N aqueous hydrogen chloride solution. The resulting mixture was extracted with diethyl ether. The organic extract was washed with water and brine, dried over magnesium sulfate, and concentrated to yield 1{(2-ethoxycarbonylethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentane carboxylic acid benzyl ester as a yellow semi-solid (149.1 grams, 96%).

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-e3fe7c3176904c70b78ab13ec6fe6275
出典メモuspto-grants-2001_04