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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16309생성일: 2026년 10월 24일

3-Hydroxypyridine → 6-(Pyridin-3-yloxy)-N-(3,4,5-trimethoxyphenyl)pyrazin-2-amine

https://huagongshe.com/ko/reaction/16309

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참여 물질

역할이름HCID투입량
반응물3-HydroxypyridineHCID 7971—
반응물2-(3,4,5-Trimethoxyphenylamino)-6-chloropyrazineHCID 11609049—
생성물6-(Pyridin-3-yloxy)-N-(3,4,5-trimethoxyphenyl)pyrazin-2-amineHCID 2487920626%

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Using Method X with 150 mg of 2-(3,4,5-trimethoxyphenylamino)-6-chloropyrazine and 3-hydroxypyridine, the title compound was obtained (46 mg). Yield: 26%. 1H NMR (250 MHz, DMSO-d6) δ 3.41 (s, 6H), 3.54 (s, 3H), 6.71 (s, 2H), 7.47 (ddd, 1H, J1=0.6 Hz, J2=4.7 Hz, J3=8.4 Hz), 7.69 (ddd, 1H, J1=1.4 Hz, J2=2.8 Hz, J3=8.4 Hz), 7.82 (s, 1H), 7.98 (s, 1H), 8.43 (dd, 1H, J1=1.4 Hz, J2=4.7 Hz), 8.54 (dd, 1H, J1=0.5 Hz, J2=2.8 Hz), 9.61 (s, 1H). 13C NMR (62.9 MHz, DMSO-d6) δ 55.32, 60.04, 95.95, 120.94, 124.52, 128.42, 128.91, 132.34, 136.10, 142.68, 145.66, 150.31, 150.38, 152.71, 156.84. m/z 355.1 [(M+H)+ calcd for C18H18N4O4 354.1].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737152B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2745ade71a36470b9c18b908d39569ea
출처 메모uspto-grants-2010_06