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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446673Generated: October 25, 2026

Acetic Acid → HCID 57448664, compound

https://huagongshe.com/reaction/446673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethyl SulfoxideHCID 679—
ReactantSodium MethoxideHCID 10942334—
ReactantN-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamideHCID 57448672—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 57448664HCID 57448664—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a crude product of N-{3-[(2,6-dichloropyridin-4-yl)amino]quinoxalin-2-yl}-3-nitrobenzenesulfonamide (1.24 g) prepared using procedures similar to those for Example 151, was added anhydrous DMSO (10 mL), followed by sodium methoxide (273 mg). The resulting mixture was heated at 100° C. for 3 days. The mixture was diluted with EtOAc and water, and the pH was adjusted to about 4 by adding acetic acid. The product was extracted with EtOAc (3×). The combined extracts were washed with brine to give the crude product. A portion of the crude product was purified by prep HPLC to give N-(3-{[2-chloro-6-(methyloxy)pyridin-4-yl]amino}quinoxalin-2-yl)-3-nitrobenzenesulfonamide. 1H NMR (400 MHz, DMSO) δ 9.44 (s, 1H), 8.90 (s, 1H), 8.50 (d, 1H), 8.42 (d, 1H), 7.88-7.84 (m, 2H), 7.77 (s, 1H), 7.74 (s, 1H), 7.64 (d, 1H), 7.45-7.38 (m, 2H), 3.82 (s, 3H); MS (EI) m/z for C20H15ClN6O5S: 496.94 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481001B2
Source datasetuspto-grants-2013_07
ORD IDord-ee725ae26a1c4ee0ab0d766470fb3701
Source noteuspto-grants-2013_07