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HRID 14920作成日:2026年10月24日

3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- → N-(3-{2-[2-(3-Chloro-4-hydroxy-phenyl)-ethylamino]pyrimidin-4-yl}-benzyl)-N-isopropyl-4-trifluoromethyl-nicotinamide

https://huagongshe.com/ja/reaction/14920

反応式

関与物質

役割名称HCID仕込み量
反応物3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-HCID 2777549—
反応物2-Chloro-4-(2-{4-[3-(isopropylamino-methyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenolHCID 58603441—
生成物N-(3-{2-[2-(3-Chloro-4-hydroxy-phenyl)-ethylamino]pyrimidin-4-yl}-benzyl)-N-isopropyl-4-trifluoromethyl-nicotinamideHCID 58603776—

反応手順

2-Chloro-4-(2-{4-[3-(isopropylamino-methyl)-phenyl]-pyrimidin-2-ylamino}-ethyl)-phenol (compound 132) was coupled with 4-trifluoromethyl-nicotinic acid following procedure D2. LC-MS showed the product had the expected M+H+ of 570. 1H NMR (Varian 300 MHz, CDCl3, shifts relative to the solvent peak at 7.24 ppm) δ 9.4 (s, 1H)) 9.0 (d, 1H) 8.4 (s, 1H) 8.3 (d, 1H) 8.1 (s, 1H) 7.9 (d, 1H) 7.7 (d, 1H) 7.5 (m, 1H) 7.4 (m, 2H) 7.2 (s, 1H) 6.9 (d, 1H) 5.7 (s, br, 1H) 3.9 (s, 2H) 3.7 (m, 2H) 3.1 (m, 1H) 2.9 (m, 2H) 1.2 (d, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732444B2
出典データセットuspto-grants-2010_06
ORD IDord-8c7099a07627400ba279fe379a8525f6
出典メモuspto-grants-2010_06