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HRID 237362作成日:2026年10月25日

Hydrochloric Acid → N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/237362

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 CarbonateHCID 11430—
反応物2,3-DichloroquinoxalineHCID 16659—
反応物Benzenesulfonamide, 3-nitro-HCID 67138—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5007601—

反応条件

温度150 °C

反応手順

2,3-Dichloroquinoxaline (26.1 g, 131.1 mmol), m-Nitrobenzene sulfonamide (26.5 g, 131.1 mmol) and potassium carbonate (18.1 g, 131.1) were dissolved in anhydrous DMSO (500 mL). The reaction was heated to 150° C. for 2 h. The reaction mixture was poured into water (400 mL), followed by addition of 2M HCl (60 mL). The product was extracted with EtOAc (3×500 mL). The organic layers were combined and washed water (2×500 mL) and brine (2×500 mL). The product was then dried with sodium sulfate to give N-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamide. MS (EI) for C14H9ClN4O4S: 364.94, 366.97 (MH+)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642584B2
出典データセットuspto-grants-2014_02
ORD IDord-c2d2f7f0d90d43d5b762d39a4c2ce1a8
出典メモuspto-grants-2014_02