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HRID 1855455作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-chloro-4-methyl-6-(N-methyl-2-hydroxyethylamino)pyrimidineHCID 18323828—
反応物3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
生成物2-({2-[3-Methoxy-4-(4-methyl-imidazol-1-yl)-phenylamino]-6-methyl-pyrimidin-4-yl}-methyl-amino)-ethanolHCID 4419328057%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08962834B2
出典データセットuspto-grants-2015_02
ORD IDord-e4a91c00ee7c415ab49b058a3e7bea80
出典メモuspto-grants-2015_02