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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323801생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/323801

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물Potassium CarbonateHCID 11430—
반응물1{(2-Carboxyethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentanecarboxylic acid benzyl esterHCID 15524281—
용매DimethylformamideHCID 6228—
생성물1{(2-Ethoxycarbonylethyl)-[4-(4-fluorophenoxy)benzenesulfonyl]amino}cyclopentane carboxylic acid benzyl esterHCID 1552428296.4%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214872B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-e3fe7c3176904c70b78ab13ec6fe6275
출처 메모uspto-grants-2001_04