戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 42650作成日:2026年10月24日

Potassium Carbonate → 2-(5-(3,4-dimethoxy-5-nitrophenyl)-1H-imidazol-1-yl)-5-(trifluoromethyl)pyridine

https://huagongshe.com/ja/reaction/42650

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Tosylmethyl isocyanideHCID 161915—
反応物2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
反応物3,4-Dimethoxy-5-nitrobenzaldehydeHCID 10867565—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-(5-(3,4-dimethoxy-5-nitrophenyl)-1H-imidazol-1-yl)-5-(trifluoromethyl)pyridineHCID 68701968—

反応手順

To a stirred solution of 5-(trifluoromethyl)pyridin-2-amine (0.405 g, 2.5 mmol) in a mixture of ethanol (12.5 mL) and acetic acid (0.25 mL) at room temperature was added 3,4-dimethoxy-5-nitrobenzaldehyde (0.53 g, 2.5 mmol). The reaction was heated at reflux temperature for two hours then ethanol was evaporated. The oily residue was dissolved in a mixture of methanol (17 mL) and 1,2-dimethoxyethane (7.5 mL), whereupon 1-(isocyanomethylsulfonyl)-4-methylbenzene (TOSMIC) (0.73 g, 3.75 mmol) and potassium carbonate (0.69 g, 5 mmol) were added in one portion. The resulting mixture was stirred at reflux temperature for 3 hours. The reaction was evaporated to dryness, and then taken up in dichloromethane (50 ml). The organic phase was washed with water (50 mL) and then dried over anhydrous magnesium sulphate, filtered and evaporated to leave brown oil. Column chromatography over silica gel (petroleum ether-ethyl acetate 9:1) gave 2-(5-(3,4-dimethoxy-5-nitrophenyl)-1H-imidazol-1-yl)-5-(trifluoromethyl)pyridine, 0.542 g (55%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536203B2
出典データセットuspto-grants-2013_09
ORD IDord-5fe24992b3e64f0c88110d47cb693837
出典メモuspto-grants-2013_09