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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1522164생성일: 2026년 10월 26일

3-Aminophenol → N-(3-((6-amino-5-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrimidin-4-yl)oxy)phenyl)acrylamide

https://huagongshe.com/reaction/1522164

반응식

참여 물질

역할이름HCID투입량
반응물3-AminophenolHCID 11568—
반응물Acryloyl chlorideHCID 13140—
반응물5,6-Dichloro-pyrimidin-4-ylamineHCID 24219262—
반응물1-(4-methoxybenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 53440213—
생성물N-(3-((6-amino-5-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrimidin-4-yl)oxy)phenyl)acrylamideHCID 86721771—

반응 단계

N-(3-((6-amino-5-(1-(4-methoxybenzyl)-1H-pyrazol-4-yl)pyrimidin-4-yl)oxy)phenyl)acrylamide was prepared from 5,6-dichloropyrimidin-4-amine, 3-aminophenol, 1-(4-methoxybenzyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, and acryloyl chloride using methods A, C, and F. HPLC purity: 99%. MS: m/z=443 [M+H]+. 1H-NMR (DMSO-d6) δ 10.21 (s, 1H), 8.08 (s, 1H), 8.01 (s, 1H), 7.70 (s, 1H), 7.50 (s, 1H), 7.41 (d, 1H), 7.33-7.26 (m, 3H), 6.90 (d, 2H), 6.83-6.58 (m, 2.5H), 6.40 (dd, 1H), 6.25 (d, 1H), 5.76 (d, 1H), 5.28 (s, 2H), 3.73 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073947B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-9ef174e7d1e74dd79b41c33f74b82df1
출처 메모uspto-grants-2015_07