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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 387745생성일: 2026년 10월 25일

Potassium Carbonate → 6,7-Dimethoxy-4-(5-nitro-pyridin-2-yloxy)-quinoline

https://huagongshe.com/reaction/387745

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-Bromo-5-nitropyridineHCID 78240—
반응물6,7-Dimethoxy-4-hydroxyquinolineHCID 459611—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물6,7-Dimethoxy-4-(5-nitro-pyridin-2-yloxy)-quinolineHCID 2293625134.1%

반응 단계

6,7-Dimethoxy-1,4-dihydro-4-quinolinone (4.10 g, 20.0 mmol), 2-bromo-5-nitropyridine (4.46 g, 22.0 mmol) and potassium carbonate (5.53 g, 40.0 mmol) were heated and stirred at 70° C. for 3 hours in N,N-dimethylformamide (20 ml). The reaction solution was diluted with ethyl acetate, the insoluble portion was filtered off, and after washing with water and saturated saline and drying the organic layer over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was distilled off under reduced pressure. The obtained crude product was subjected to silica gel column chromatography (eluent: ethyl acetate), and the fraction containing the target substance was concentrated, suspended in ethyl acetate and diluted with hexane, after which the crystals were filtered out, washed with hexane and then blow-dried to obtain the title compound (2.23 g, 6.81 mmol, 34%) as yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08372981B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-f00eee7b12e14240881234f9afacc957
출처 메모uspto-grants-2013_02