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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1422667생성일: 2026년 10월 27일

Triphenylphosphine → methyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylate

https://huagongshe.com/reaction/1422667

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물methyl (E)-3-[2-(3-hydroxymethylphenyl)pyrimidin-5-yl]acrylateHCID 58289762—
반응물6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-oneHCID 59406809—
용매TetrahydrofuranHCID 8028—
생성물methyl (E)-3-(2-{3-[6-oxo-3-(3,4,5-trifluorophenyl)-6H-pyridazin-1-ylmethyl]phenyl}pyrimidin-5-yl)acrylateHCID 59484916—

반응 단계

47.2 90 mg (0.4 mmol) of 6-(3,4,5-trifluorophenyl)-2H-pyridazin-3-one and 111 mg (0.41 mmol) of methyl (E)-3-[2-(3-hydroxymethylphenyl)pyrimidin-5-yl]acrylate are suspended in 3 ml of THF with 200 mg (0.6 mmol) of polymer-bound triphenylphosphine (about 3 mmol of triphenylphosphine per g), and the mixture is shaken at room temperature for 30 min. The mixture is cooled to 0° C., and 95 μl (0.6 mmol) of diethyl azodicarboxylate are added. The reaction mixture is shaken at room temperature for 24 h. The reaction mixture is purified by means of preparative HPLC; yield: 7 mg of “A283”; HPLC: Rt=3.41 min (method C); LC-MS: 479 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08927540B2
출처 데이터셋uspto-grants-2015_01
ORD IDord-24ba6300cd5b4f4b8023b62ee6449991
출처 메모uspto-grants-2015_01