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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59153생성일: 2026년 10월 24일

2-(Dicyclohexylphosphino)biphenyl → N2-(3-Methoxy-4-(6-methylpyridazin-4-yl)phenyl)-N4-methyl-6-((2,2,2-trifluoroethoxy)-methyl)pyrimidine-2,4-diamine

https://huagongshe.com/ko/reaction/59153

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참여 물질

역할이름HCID투입량
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물CesiumHCID 5354618—
반응물3-Methoxy-4-(6-methylpyridazin-4-yl)anilineHCID 66859066—
반응물2-Chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amineHCID 117821210—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물N2-(3-Methoxy-4-(6-methylpyridazin-4-yl)phenyl)-N4-methyl-6-((2,2,2-trifluoroethoxy)-methyl)pyrimidine-2,4-diamineHCID 86344800—

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온도120 °C

반응 단계

A mixture of 2-chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amine (50 mg, 0.20 mmol), 3-methoxy-4-(6-methylpyridazin-4-yl)aniline (42 mg, 0.20 mmol), cesium rbonate (127 mg, 0.39 mmol), palladium (II) acetate (7 mg, 0.03 mmol) and 2-(dicyclohexylphosphino)-biphenyl (10 mg, 0.03 mmol) in dioxane (2 mL) was heated under argon at 120° C. for 90 minutes in a microwave reactor. 2-Chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amine (72 mg, 0.28 mmol, 1.4 eq), palladium(II) acetate (7 mg) and 2-(dicyclohexylphosphino)biphenyl (10 mg) was added and the mixture was heated at 120° C. for 90 minutes in a microwave reactor. The mixture was filtered through a short silica gel plug which was washed with 10% solution of methanol in ethyl acetate (75 mL). The eluate was concentrated in vacuum and the residue was purified by preparative to give the title compound as a solid, 22 mg (26%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439904B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-766617a20112464390c873db4aff3d00
출처 메모uspto-grants-2016_09