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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 42650생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tosylmethyl isocyanideHCID 161915—
반응물2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
반응물3,4-Dimethoxy-5-nitrobenzaldehydeHCID 10867565—
용매Acetic AcidHCID 176—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매1,2-DimethoxyethaneHCID 8071—
생성물2-(5-(3,4-dimethoxy-5-nitrophenyl)-1H-imidazol-1-yl)-5-(trifluoromethyl)pyridineHCID 68701968—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536203B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-5fe24992b3e64f0c88110d47cb693837
출처 메모uspto-grants-2013_09