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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230331생성일: 2026년 10월 23일

Potassium Carbonate → (E)-2-(2,6-dichlorobenzamido)-5-[4-(4-hydroxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester

https://huagongshe.com/ko/reaction/230331

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tri-o-tolylphosphineHCID 80271—
반응물tetrahydro-4-(4-iodophenyl)-2H-pyran-4-olHCID 57033480—
반응물2-(2,6-Dichlorobenzamido)pent-4-enoic acid methyl esterHCID 57762518—
촉매palladium(II) acetateHCID 167845—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(E)-2-(2,6-dichlorobenzamido)-5-[4-(4-hydroxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl esterHCID 248572845.9%

반응 조건

온도80 °C

반응 단계

Under an argon atmosphere, palladium acetate (4.7 mg) and tris(2-methylphenyl)phosphine (6.1 mg) were added to a suspension of 2-(2,6-dichlorobenzamido)pent-4-enoic acid methyl ester (60.4 mg), tetrahydro-4-(4-iodophenyl)-2H-pyran-4-ol (60.8 mg) and potassium carbonate (41.5 mg) in DMF (4 ml), and the resulting mixture was stirred at 80° C. for 6 hours. After cooling the reaction solution to room temperature, ethyl acetate was added thereto and the solution was washed 3 times with water and once with saturated brine, followed by drying the organic layers 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→1/4) and thereafter by thin layer chromatography (silica gel, mobile phase: cyclohexane/ethyl acetate=1/1) to obtain (E)-2-(2,6-dichlorobenzamido)-5-[4-(4-hydroxytetrahydropyran-4-yl)-phenyl]pent-4-enoic acid methyl ester (5.6 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566724B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-7d492876e34741779d9ef2708bb725eb
출처 메모uspto-grants-2009_07