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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473701생성일: 2026년 10월 24일

4-Aminophenol → 1-(4-(3-(4-Aminophenoxy)pyrazin-2-yl)piperidin-1-yl)ethanone

https://huagongshe.com/ko/reaction/473701

반응식

참여 물질

역할이름HCID투입량
반응물4-AminophenolHCID 403—
반응물Cesium carbonateHCID 10796—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물HCID 59351287HCID 59351287—
용매Ethyl AcetateHCID 8857—
생성물1-(4-(3-(4-Aminophenoxy)pyrazin-2-yl)piperidin-1-yl)ethanoneHCID 59374162—

반응 조건

온도80 °C

반응 단계

1-(4-(3-fluoropyrazin-2-yl)piperidin-1-yl)ethanone (0.153 g, 0.685 mmol), 4-aminophenol (0.079 g, 0.720 mmol), cesium carbonate (0.246 g, 0.754 mmol), and 1-methyl-2-pyrrolidinone (0.685 mL, 0.685 mmol) were combined in a sealed tube and heated at 80° C. for 20 h. The cooled reaction mixture was diluted with EtOAc and washed with water; the aqueous layer was back-extracted with EtOAc (1×). The organic layers were combined, dried (MgSO4), filtered, and concentrated in vacuo. ISCO purification (20% to 80% EtOAc/Hexanes) afforded 1-(4-(3-(4-aminophenoxy)pyrazin-2-yl)piperidin-1-yl)ethanone as a light brown oil. MS (ESI, pos. ion) m/z: 313.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637500B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-309c1eeab3ee4f1b8e3e89c29bc0b0db
출처 메모uspto-grants-2014_01