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HRID 387745作成日:2026年10月26日

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

https://huagongshe.com/reaction/387745

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2-Bromo-5-nitropyridineHCID 78240—
反応物6,7-Dimethoxy-4-hydroxyquinolineHCID 459611—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物6,7-Dimethoxy-4-(5-nitro-pyridin-2-yloxy)-quinolineHCID 2293625134.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08372981B2
出典データセットuspto-grants-2013_02
ORD IDord-f00eee7b12e14240881234f9afacc957
出典メモuspto-grants-2013_02