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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530409생성일: 2026년 10월 27일

Ethyl Acetate → Methyl 4-hydroxy-3'-methyl-5'-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-3-carboxylate

https://huagongshe.com/reaction/530409

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium CarbonateHCID 10340—
반응물Methyl 5-IodosalicylateHCID 248910—
반응물N-(3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-(trifluoromethyl)pyrimidin-2-amineHCID 58456089—
촉매HCID 178477754HCID 178477754—
용매WaterHCID 962—
생성물Methyl 4-hydroxy-3'-methyl-5'-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-3-carboxylateHCID 90041756—

반응 조건

온도80 °C

반응 단계

A mixture of methyl 2-hydroxy-5-iodobenzoate (11.6 g, 41.5 mmol) in 2-methyl-THF (180 mL) and water (82.5 mL) was purged with N2 for 30 minutes. Sodium carbonate (12.6 g, 119 mmol), N-[3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-4-(trifluoromethyl)pyrimidin-2-amine (15.0 g, 39.6 mmol) and [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (1.61 g, 1.98 mmol) were added to the reaction mixture at rt under N2 and then the mixture was heated to 80° C. for 14 hours. The reaction mixture was poured into a 1:1 solution of ethyl acetate/2N HCl (800 mL) and the layers were separated. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residue was purified by silica gel column chromatography (ethyl acetate/hexanes) to afford methyl 4-hydroxy-3′-methyl-5′-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-3-carboxylate. MS ESI calcd. for C20H12F3N3O3 [M+H]+ 404, found 404.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09353066B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-a68f91da7b164762ab11fcc32388105c
출처 메모uspto-grants-2016_05