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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331193Generated: October 25, 2026

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

https://huagongshe.com/reaction/331193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloroquinoxalineHCID 16659—
Reactantm-ToluenesulphonamideHCID 74697—
SolventDimethylacetamideHCID 31374—
ProductN-(3-chloroquinoxalin-2-yl)-3-methylbenzenesulfonamideHCID 420029165.7%

Reaction Conditions

Temperature170 °C

Reaction Steps

A suspension of 2,3-dichloroquinoxaline (500 mg; 2.5 mmol; 1 eq), 3-methylbenzene sulfonamide (430.1 mg, 2.5 mmol, 1 eq.), dry K2CO3 (347.2 mg, 2.5 mmol, 1 eq.) in DMA (5 ml) is heated up at 170° C. in the microwave for 30 min under normal absorption. The solvent is evaporated to dryness. Water (20 ml) is added then AcOH until acidic pH. The residual suspension is left at 4° C. for 1 h and the precipitate formed is filtered off, washed with water until neutral, then ACN and dried under vacuum at 40° C. overnight, to afford 548.3 mg (65%) of the title compound. 1H NMR (DMSO-d6) δ 11.53 (brs, 1H), 7.99 (m, 2H), 7.87 (t, J=8.6 Hz, 2H), 7.77 (dt, J=1.5, 7.5 Hz, 1H), 7.67 (t, J=8.0 Hz, 1H), 7.56-7.43 (m, 2H), 2.42 (s, 3H). HPLC (max plot) 99%; Rt 3.70 min. LC/MS: (ES+): 334.2, (ES−): 332.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877757B2
Source datasetuspto-grants-2014_11
ORD IDord-079c40edb76b49d1abd5d71b77b97614
Source noteuspto-grants-2014_11