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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230367생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/230367

반응식

참여 물질

역할이름HCID투입량
반응물2-(4-Iodophenoxy)pyrimidineHCID 1484617—
반응물2-(2,6-Dichlorobenzamido)pent-4-ynoic acid methyl esterHCID 20610296—
촉매Copper iodideHCID 83717—
촉매HCID 178418476HCID 178418476—
용매THF diisopropylamineHCID 18968793—
생성물2-(2,6-Dichlorobenzamido)-5-[4-(pyrimidin-2-yloxy)phenyl]pent-4-ynoic acid methyl esterHCID 5776247786.2%

반응 단계

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), 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 10=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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566724B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-1356b306c5a748a58c42535df6be0692
출처 메모uspto-grants-2009_07