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HRID 8134作成日:2026年10月24日

Ethyl Acetate → Methyl 4-{[{2-[(4'-chloro[1,1'-biphenyl]-4-yl)methoxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoate

https://huagongshe.com/ja/reaction/8134

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium CarbonateHCID 10340—
反応物4-Chlorophenylboronic acidHCID 74299—
反応物{[{2-[(4-Bromobenzyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoateHCID 86760181—
触媒HCID 178418476HCID 178418476—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Methyl 4-{[{2-[(4'-chloro[1,1'-biphenyl]-4-yl)methoxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoateHCID 22015030—

反応手順

300.0 mg (0.51 mmol) of methyl 4-({[{2-[(4-bromobenzyl)oxy]phenethyl}(5-ethoxy-5-oxopentyl)amino]methyl}benzoate from Ex. 4 are initially charged in 3 ml of dimethoxyethane and admixed successively with 101.7 mg (0.62 mmol) of 4-chlorophenylboronic acid and 0.57 ml of 2M sodium carbonate solution. 10.0 mg of dichlorobis(triphenylphosphine)palladium(II) are added, and the mixture is then heated at reflux temperature for 18 hours. The reaction solution is cooled, admixed with 20 ml of ethyl acetate and washed successively with 5% strength sodium hydrogen phosphate solution, water and saturated sodium chloride solution. The organic phase is dried over magnesium sulphate and the solvent is distilled off under reduced pressure. The crude product is chromatographed over silica gel using the mobile phase cyclohexane/ethyl acetate=10:1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087644B1
出典データセットuspto-grants-2006_08
ORD IDord-5d34544f0aa64138a4ebdecdb4794fce
出典メモuspto-grants-2006_08