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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669951Generated: October 30, 2026

Hydrochloric Acid → HCID 698553, compound

https://huagongshe.com/reaction/1669951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfonamideHCID 7370—
ReactantCesium carbonateHCID 10796—
Reactant2,3-DichloroquinoxalineHCID 16659—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 698553HCID 698553—

Reaction Conditions

Temperature150 °C

Reaction Steps

A flask was charged with 2,3-dichloroquinoxaline (3.5 g, 18 mmol), 85 mL of dimethylsulfoxide, benzene sulfonamide (2.8 g, 18 mmol), and cesium carbonate (5.8 g, 18 mmol). The reaction mixture was stirred under an N2 atmosphere for 15 h at 150° C., after which time, it was transferred to a separatory funnel and 100 mL of water were added. Concentrated HCl was then added in order to acidify the reaction mixture to pH<2. The aqueous layer was subsequently washed three times with 90 mL ethyl acetate. The ethyl acetate layers were then washed two times with 150 mL water, three times with 100 mL brine and then dried over sodium sulfate. The ethyl acetate was removed on a rotary-evaporator. A slurry was formed by adding ethyl acetate and dichloromethane to the dried crude product, filtration yielded N-(3-chloroquinoxalin-2-yl)-benzenesulfonamide which was used without further purification. MS (EI) m/z C14H10ClN3O2S: 319.9 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989622B2
Source datasetuspto-grants-2011_08
ORD IDord-ef01fca9fe8345c4b7790ce18ef321c8
Source noteuspto-grants-2011_08