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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404813생성일: 2026년 10월 24일

3-Methoxyphenol → N2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine

https://huagongshe.com/ko/reaction/404813

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxyphenolHCID 9007—
반응물Potassium CarbonateHCID 11430—
반응물N2-(6-chloropyrimidin-4-yl)pyridine-2,6-diamineHCID 57708264—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamineHCID 5770823140.7%

반응 조건

온도100 °C

반응 단계

To a solution of N2-(6-chloropyrimidin-4-yl)pyridine-2,6-diamine (200 mg, 0.90 mmol) in dry DMF (2 mL) was added 3-methoxyphenol (112 mg, 0.90 mmol) and anhydrous K2CO3 (186 mg, 1.353 mmol). The reaction mixture was heated at 100° C. for 16 h under N2 atmosphere. It was then cooled and DMF removed under reduced pressure to give a yellowish gummy residue that was taken in EtOAc (10 mL). It was washed with water (5 mL), brine (5 mL), dried over Na2SO4 and then concentrated under reduced pressure to give a crude product. This was further purified by column chromatography (SiO2, 60-120, hexane/EtOAc, 5/5) to give N2-(6-(3-methoxylphenoxy)pyrimidin-4-yl)pyridine-2,6-diamine (110 mg, 40.7%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748606B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-085fc37d00d94cbab6701e9d978d0e48
출처 메모uspto-grants-2014_06