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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 323798생성일: 2026년 10월 25일

CID 66185 → 1-{[3-(Tert-butyl-dimethylsilanyloxy)-propyl]-[4-(4-fluorophenoxy)benzenesulfonyl]-amino}cyclopentanecarboxylic acid benzyl ester

https://huagongshe.com/reaction/323798

반응식

참여 물질

역할이름HCID투입량
반응물CID 66185HCID 66185—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
반응물1-[4-(4-Fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl esterHCID 11005171—
반응물Tert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
용매DimethylformamideHCID 6228—
생성물1-{[3-(Tert-butyl-dimethylsilanyloxy)-propyl]-[4-(4-fluorophenoxy)benzenesulfonyl]-amino}cyclopentanecarboxylic acid benzyl esterHCID 15524279103.7%

반응 단계

To a solution of 1-[4-(4-fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl ester (199 grams, 0.42 mole) in dry N,N-dimethylformamide (2.5 L) at room temperature was added potassium hexamethyldisilazide (100 grams, 0.50 mole) and, after 3 hours, tert-butyl-(3-iodopropoxy)dimethylsilane (150 grams, 0.50 mole). The resulting mixture was stirred at room temperature for 16 hours. Additional tert-butyl-3-iodopropoxy)-dimethylsilane (20 grams, 0.067 mole) was then added. Stirring at room temperature was continued for a further 3.5 hours. The mixture was quenched by addition of saturated ammonium chloride solution. The N,N-dimethylformamide was removed by evaporation under vacuum. The residue was taken up in diethyl ether and washed with water and brine. After drying over magnesium sulfate, the diethyl ether was evaporated to afford crude 1-{[3-(tert-butyl-dimethylsilanyloxy)-propyl]-[4-(4-fluorophenoxy)benzenesulfonyl]-amino}cyclopentanecarboxylic acid benzyl ester as an amber oil (279.6 grams).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214872B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-91d9b349d20c410ea7159b4f5418a3a7
출처 메모uspto-grants-2001_04