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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59151생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/59151

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-(Dicyclohexylphosphino)biphenylHCID 2734216—
반응물3-Methoxy-4-(6-methylpyridazin-4-yl)anilineHCID 66859066—
반응물2-Chloro-4-(4,4-difluoropiperidin-1-yl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidineHCID 117821130—
촉매palladium(II) acetateHCID 167845—
용매1,4-DioxaneHCID 31275—
생성물4-(4,4-Difluoropiperidin-1-yl)-N-(3-methoxy-4-(6-methylpyridazin-4-yl)phenyl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-2-amineHCID 86344804—

반응 조건

온도120 °C

반응 단계

A mixture of 2-chloro-4-(4,4-difluoropiperidin-1-yl)-6-((2,2,2-trifluoroethoxy)methyl)pyrimidine (40 mg, 0.12 mmol), 3-methoxy-4-(6-methylpyridazin-4-yl)aniline (25 mg, 0.12 mmol), cesium carbonate (75 mg, 0.23 mmol), palladium(II) acetate (4 mg, 0.02 mmol) and 2-(dicyclohexylphosphino)biphenyl (6 mg, 0.02 mmol) in dioxane (2 mL) was heated under argon 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) and the eluate was concentrated in vacuum. The residue was purified by preparative HPLC to give the title compound as a solid, 35 mg (58%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439904B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-d34d6ade3ddc4011a1057bfd59a5a48f
출처 메모uspto-grants-2016_09