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HRID 323798作成日:2026年10月26日

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

https://huagongshe.com/reaction/323798

反応式

関与物質

役割名称HCID仕込み量
反応物CID 66185HCID 66185—
反応物Potassium bis(trimethylsilyl)amideHCID 3251421—
反応物1-[4-(4-Fluorophenoxy)benzenesulfonylamino]-cyclopentanecarboxylic acid benzyl esterHCID 11005171—
反応物Tert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
溶媒DimethylformamideHCID 6228—
生成物1-{[3-(Tert-butyl-dimethylsilanyloxy)-propyl]-[4-(4-fluorophenoxy)benzenesulfonyl]-amino}cyclopentanecarboxylic acid benzyl esterHCID 15524279103.7%

反応手順

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).

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-91d9b349d20c410ea7159b4f5418a3a7
出典メモuspto-grants-2001_04