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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44204Generated: October 26, 2026

Nitrogen → 4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamide

https://huagongshe.com/reaction/44204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloroquinoxalineHCID 16659—
Reactant4-ChlorobenzenesulfonamideHCID 66824—
SolventDimethylformamideHCID 6228—
Product4-Chloro-N-(3-chloro-quinoxalin-2-yl)-benzenesulfonamideHCID 2366510—

Reaction Steps

To a solution of 4-Chlorobenzenesulfonamide (1.92 g, 10 mmol) in anhydrous DMF (50 mL) was added solid potassium carbonate (1.38 g, 10 mmol) in one portion. The reaction mixture was stirred for 10 minutes, followed by the addition of 2,3-dichloroquinoxaline (1.99 g, 10 mmol). Heating the resultant mixture under refux conditions in an atmosphere of N2 for 2.5 h gave the desired product. The progress of the reaction was monitored by TLC using, hexanes/EtOAc 3:1. After cooling the reaction mixture is slowly added to a vigorously stirred aqueous solution of AcOH (1%, 500 mL). The desired product precipitates as grey crystals, which are filtered and dried overnight in desiccator. Yield 2.32 g, 66%; Rf=0.7 (hexanes/EtOAc 1:1); HPLC/MS: [M+H]+ m/z 354. 1H NMR: (DMSO-d6, 600 MHz) 7.68 (t, J=7.8 Hz, 1H), 7.72 (d, J=8.4 Hz, 2H), 7.78 (td, J=7.8 Hz, J=1.2 Hz, 1H), 7.89 (d, J=8.4 Hz, 2H), 8.19 (d, J=8.4 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541415B2
Source datasetuspto-grants-2013_09
ORD IDord-668aa4d5580442bc9eb04a23c849f206
Source noteuspto-grants-2013_09