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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59097생성일: 2026년 10월 24일

Cesium carbonate → 4-(1-Ethoxyvinyl)-N-(3-methoxy-4-(6-methylpyridazin-4-yl)phenyl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-2-amine

https://huagongshe.com/ko/reaction/59097

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물3-Methoxy-4-(6-methylpyridazin-4-yl)anilineHCID 66859066—
반응물2-Chloro-4-(1-ethoxyvinyl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidineHCID 117820799—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물4-(1-Ethoxyvinyl)-N-(3-methoxy-4-(6-methylpyridazin-4-yl)phenyl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-2-amineHCID 11782104863%

반응 조건

온도120 °C

반응 단계

2-Chloro-4-(1-ethoxyvinyl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidine (0.70 g, 2.36 mmol), 3-methoxy-4-(6-methylpyridazin-4-yl)aniline (0.508 g, 2.36 mmol), cesium carbonate (1.538 g, 4.72 mmol), palladium(II) acetate (0.079 g, 0.35 mmol) and 2-(dicyclohexylphosphino)biphenyl (0.124 g, 0.35 mmol) were mixed in dioxane (16 mL). The vial was capped, evacuated and flushed with nitrogen. The reaction mixture was heated at 120° C. for 1.5 h. The mixture was filtered and the filter was washed with mixtures of methanol and DCM. The filtrate was concentrated. The residue was purified by column chromatography on silica column eluting with a gradient of methanol and DCM to give the title compound as a solid 702 mg (63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439904B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-625d0562a5f0403d9273f1fdee12028b
출처 메모uspto-grants-2016_09