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HRID 1477457作成日:2026年10月26日

Potassium Iodide → 1-(4-Methoxybenzyl)-4-oxo-1,4-dihydrocinnoline-3-carboxylic acid

https://huagongshe.com/reaction/1477457

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物4-Methyloxybenzyl chlorideHCID 69993—
反応物Ethyl 4-oxo-1,4-dihydrocinnoline-3-carboxylateHCID 23320177—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物1-(4-Methoxybenzyl)-4-oxo-1,4-dihydrocinnoline-3-carboxylic acidHCID 117776995—

反応条件

温度70 °C

反応手順

To a solution of ethyl 4-oxo-1,4-dihydrocinnoline-3-carboxylate (2.0 g), potassium iodide (1.5 g) and potassium carbonate (2.5 g) in DMF (50 mL) was added 1-(chloromethyl)-4-methoxybenzene (1.4 mL), and the mixture was stirred at 70° C. for 14 hr. The reaction mixture was diluted with water and ethyl acetate, and the organic layer was separated, washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated. The obtained residue was dissolved in ethanol-THF (1:1, 30 mL), 1 N aqueous sodium hydroxide solution (15 mL) was added, and the mixture was stirred at room temperature for 6 hr. The reaction mixture was diluted with water, neutralized with 1 N hydrochloric acid (15 mL), and the precipitate was collected by filtration, washed with water, and dried to give the title compound (1.1 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09403802B2
出典データセットuspto-grants-2016_08
ORD IDord-eb55fa673b2a458ca59a618af578cb98
出典メモuspto-grants-2016_08