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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336797Generated: October 25, 2026

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

https://huagongshe.com/reaction/336797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloroquinoxalineHCID 16659—
ReactantBenzenesulfonamide, 3-nitro-HCID 67138—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-(3-chloroquinoxalin-2-yl)-3-nitrobenzenesulfonamideHCID 5007601—

Reaction Conditions

Temperature150 °C

Reaction Steps

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) m/z for C14H9ClN4O4S: 364.94, 366.97 (MH+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889664B2
Source datasetuspto-grants-2014_11
ORD IDord-3f417f4790b34ac1b597de3477d23e6f
Source noteuspto-grants-2014_11