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HRID 1365704作成日:2026年10月25日

2-(4-Iodophenoxy)pyrimidine → 2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester

https://huagongshe.com/reaction/1365704

反応式

関与物質

役割名称HCID仕込み量
反応物2-(4-Iodophenoxy)pyrimidineHCID 1484617—
反応物2-(2,6-Dichlorobenzamido)pent-4-ynoic acid methyl esterHCID 20610296—
触媒Copper iodideHCID 83717—
触媒HCID 178418476HCID 178418476—
溶媒THF diisopropylamineHCID 18968793—
生成物2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl esterHCID 5776247786.2%

反応手順

Under an argon atmosphere, copper iodide (2.8 mg) and dichlorobis(triphenylphosphine)palladium (5.2 mg) were added to a solution of 2-(2,6-dichlorobenzamido)pent-4-ynoic acid methyl ester (74 mg) and 2-(4-iodophenoxy)pyrimidine (81 mg) in THF/diisopropylamine (3/1) mixture (5 ml), and the resulting mixture was stirred at room temperature for 2 hours. The reaction solution was concentrated and ethyl acetate was added to the residue. The insoluble matter was removed by filtration, and the filtrate was washed once with water and once with saturated brine and dried over anhydrous sodium sulfate. After removing anhydrous sodium sulfate by filtration, the filtrate was concentrated. The residue was purified by column chromatography (silica gel, eluent: cyclohexane/chloroform=2/1→cyclohexane/chloroform=1/3) to obtain 2-(2,6-dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl ester (100 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893046B2
出典データセットuspto-grants-2011_02
ORD IDord-1caf893053774d72ab85307ca4d40676
出典メモuspto-grants-2011_02