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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331192Generated: October 26, 2026

Potassium Carbonate → N-(3-chloroquinoxalin-2-yl)-3-fluorobenzenesulfonamide

https://huagongshe.com/reaction/331192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloroquinoxalineHCID 16659—
Reactant3-FluorobenzenesulfonamideHCID 150924—
SolventDimethylformamideHCID 6228—
ProductN-(3-chloroquinoxalin-2-yl)-3-fluorobenzenesulfonamideHCID 5762536584.6%

Reaction Conditions

Temperature135 °C

Reaction Steps

3-fluorobenzenesulfonamide (250 mg, 1.4 mmol), 2,3-dichloroquinoxaline (284.1 mg, 1.4 mmol) and dry K2CO3 (198.4 mg, 1.4 mmol) are dissolved in dry DMF (0.8 ml) and heated up to 135° C. in a sealed tube for 2.5 h. When TLC confirms the completion of the reaction, the reaction mixture is cooled down to rt and quenched by addition of water (4 ml) and AcOH (0.03 ml). The residue obtained is triturated and the resulting solid is filtered and washed with water until neutral pH then dried under vacuum to afford 400 mg (83%) of the title compound as an off white solid. 1H NMR (DMSO-d6) δ 12.8-10.9 (br s, 1H), 8.05-7.62 (m, 7H), 7.54 (td, J=2.0, 8.5 Hz, 1H). HPLC (max plot) 94%; Rt 3.79 min. LC/MS: (ES+): 338.1, (ES−): 336.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877757B2
Source datasetuspto-grants-2014_11
ORD IDord-c3076cf4b3dc4172a67b7cbff330ec16
Source noteuspto-grants-2014_11