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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1855455생성일: 2026년 10월 26일

2-chloro-4-methyl-6-(N-methyl-2-hydroxyethylamino)pyrimidine → 2-({2-[3-Methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-6-methyl-pyrimidin-4-yl}-methyl-amino)-ethanol

https://huagongshe.com/reaction/1855455

반응식

참여 물질

역할이름HCID투입량
반응물2-chloro-4-methyl-6-(N-methyl-2-hydroxyethylamino)pyrimidineHCID 18323828—
반응물3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
생성물2-({2-[3-Methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-6-methyl-pyrimidin-4-yl}-methyl-amino)-ethanolHCID 4419328057%

반응 단계

Prepared in analogy to example 81b) from 3-methoxy-4-(4-methyl-imidazol-1-yl)-phenylamine and 2-[(2-chloro-6-methyl-pyrimidin-4-yl)-methyl-amino]ethanol. The title compound was isolated as a colorless solid in a yield of 57%. MS ISP (m/e): 369.2 (100) [(M+H)+]. 1H NMR (CDCl3, 300 MHz): δ (ppm)=7.70 (d, 1H), 7.60 (s, 1H), 7.11 (d, 1H), 7.05-6.90 (m, 2H), 6.85 (s, 1H), 5.92 (s, 1H), 3.95-3.80 (m, 2H), 3.84 (s, 3H), 3.80-3.70 (m, 2H), 3.12 (s, 3H), 2.31 (s, 3H), 2.29 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962834B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-e4a91c00ee7c415ab49b058a3e7bea80
출처 메모uspto-grants-2015_02