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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394476생성일: 2026년 10월 25일

5-(2-Methylsulfonylpyrimidin-4-yl)-6-(3-trifluoromethylphenyl)-4,5-dihydro-2H-pyridazin-3-one → (s)-5-[2-(1-Phenylethylamino)pyrimidin-4-yl]-6-(3-trifluoromethylphenyl)-4,5-dihydro-2H-pyridazin-3-one

https://huagongshe.com/reaction/394476

반응식

참여 물질

역할이름HCID투입량
반응물5-(2-Methylsulfonylpyrimidin-4-yl)-6-(3-trifluoromethylphenyl)-4,5-dihydro-2H-pyridazin-3-oneHCID 18176613—
용매TetrahydrofuranHCID 8028—
생성물(s)-5-[2-(1-Phenylethylamino)pyrimidin-4-yl]-6-(3-trifluoromethylphenyl)-4,5-dihydro-2H-pyridazin-3-oneHCID 70023896—

반응 단계

Compound 7 (5.00 g, 13.1 mmol), s-(−)-α-methylbenzylamine (3.37 mL, 26.2 mmol) and tetrahydrofuran (100 mL) were heated to reflux under argon for 24 h. The solvent was removed in vacuo. Purification by flash column chromatography (methylene chloride:methanol: ammonium hydroxide 98:2:0.2) gave Compound 8 as a foam: 5.0 g (9.6 mmol, 73%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602872B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-92c6149c9f0046d296c6220e1fc99766
출처 메모uspto-grants-2003_08