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HRID 1488967作成日:2026年10月27日

Hydrochloric Acid → 6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1488967

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Potassium HydroxideHCID 14797—
反応物6-Fluoro-7-nitro-1,4-dihydroquinoxaline-2,3-dioneHCID 9991230—
反応物HCID 178418642HCID 178418642—
溶媒Dimethyl SulfoxideHCID 679—
生成物6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dioneHCID 986112962.9%

反応条件

温度130 °C

反応手順

First, 9.007 g of 7-fluoro-6-nitro-1,4-dihydroquinoxaline-2,3-dione, 7.611 g of 4-hydroxypyridine, and 5.219 g of powdered potassium hydroxide were added to 120 ml of dry dimethylsulfoxide. The mixture was stirred at 130° C. for 2 hours in a nitrogen atmosphere. Then, 50 ml of ice water and 30 ml of 4N hydrochloric acid were added to the reaction mixture so as to make it weakly acidic (pH 3 to 4). The resultant yellow precipitate was filtered and washed with water. The precipitate was dissolved by heating in a mixture containing 560 ml of water and 56 ml of conc. aqueous ammonia. One gram of activated carbon was added to the resultant mixture, stirred, and filtered. The filtrate was neutralized with conc. hydrochloric acid and ice-cooled. The precipitated crystals were then filtered and washed with water, methanol, and ethanol, successively. The resultant crystals were dried to give 7.56 g of 6-nitro-7-(4-oxo-4H-pyridin-1-yl)-1,4-dihydroquinoxaline-2,3-dione (hereinafter, abbreviated as Ia).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05677305
出典データセットuspto-grants-1997_10
ORD IDord-08ff0463da474729a90d3320dd332b50
出典メモuspto-grants-1997_10