돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 911150생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/911150

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 번호US08022221B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-9b462b1b6c944bc8881b404f1916135c
출처 메모uspto-grants-2011_09