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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57044생성일: 2026년 10월 24일

N-Methylaniline → 4-({2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-methyloxetan-3-yl)propanoyl}amino)benzoic acid

https://huagongshe.com/ko/reaction/57044

반응식

참여 물질

역할이름HCID투입량
반응물N-MethylanilineHCID 7515—
반응물Allyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-methyloxetan-3-yl)propanoyl}amino)benzoateHCID 117622716—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물4-({2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-methyloxetan-3-yl)propanoyl}amino)benzoic acidHCID 117622630—

반응 단계

25 mg (44 μmol) of allyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-3-(3-methyloxetan-3-yl)propanoyl}amino)benzoate (racemate) and 48.2 μl (445 μmol) of N-methylaniline were initially charged in 1 ml of tetrahydrofuran, and the resulting solution was degassed. 5 mg (4 μmol) of tetrakis(triphenylphosphine)palladium(0) were then added, and the mixture was stirred at room temperature for another 30 min. The reaction solution was purified directly by preparative HPLC (neutral) and the title compound was obtained after final preparative thin-layer chromatography (ethyl acetate/cyclohexane=1:1). Yield: 10.1 mg (purity 92%, 42% of theory)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434690B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-af24f9f725cd417796d95e5001752d0f
출처 메모uspto-grants-2016_09