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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2361056생성일: 2026년 10월 27일

4-Aminophenol → 4-{3-[2-(Methylthio)pyrimidin-4-yl]pyridin-2-yloxy}benzeneamine

https://huagongshe.com/reaction/2361056

반응식

참여 물질

역할이름HCID투입량
반응물4-AminophenolHCID 403—
반응물Cesium carbonateHCID 10796—
반응물4-(2-Chloropyridin-3-yl)-2-(methylthio)pyrimidineHCID 57756239—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물4-{3-[2-(Methylthio)pyrimidin-4-yl]pyridin-2-yloxy}benzeneamineHCID 66731913—

반응 조건

온도130 °C

반응 단계

A resealable pressure bottle was charged with 4-(2-chloropyridin-3-yl)-2-(methylthio)pyrimidine (6.00 g, 25.2 mmol), 4-aminophenol (2.89 g, 26.5 mmol), and cesium carbonate (16.4 g, 50.5 mmol). These reagents were suspended in DMSO (50.5 ml, 0.50 M). The vessel was sealed and heated to 130° C. for 48 hrs. Reaction mixture was allowed to cool to RT, diluted with water and extracted with EtOAc. The organic layer was collected, dried with Na2SO4, filtered, and concentrated to give a light brown residue, which was purified by silica gel chromatography (ISCO, 10% to 50% Ethyl Acetate/Hexanes) to afford clean material as light yellow solid. MS m/z=311 [M+H]+. Calc'd for C16H14N4OS: 310.37.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08686155B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-ebf22e9db3684b33b20e24ba192ef316
출처 메모uspto-grants-2014_04