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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336795Generated: October 29, 2026

Hydrochloric Acid → HCID 59249031, compound

https://huagongshe.com/reaction/336795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 25102201HCID 25102201—
SolventEthyl AcetateHCID 8857—
ProductHCID 59249031HCID 5924903194%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of N-(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)-3-cyanobenzenesulfonamide (6.02 g, 12.95 mmol), prepared using procedures similar to those in Example 115 or Example 423, in methanol (20 mL) and 1,4-dioxane (20 mL) was added 6.0 N aqueous sodium hydroxide (40 mL) at room temperature. The solution was stirred at 90° C. for 3.5 h. The reaction was cooled to room temperature and neutralized slowly by adding 2.0 N hydrochloric acid until the pH of the solution became in the 2-3 range at 0° C. The solution was diluted with ethyl acetate (300 mL). The organic layer was washed with saturated aqueous sodium chloride (50 mL) and dried over magnesium sulfate. Filtration and concentration at reduced pressure afforded 3-{[(3-{[2-chloro-5-(methoxy)-phenyl]amino}quinoxalin-2-yl)amino]sulfonyl}benzoic acid (5.921 g, 94%). MS (EI) m/z for C22H17ClN4O5S: 485.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889664B2
Source datasetuspto-grants-2014_11
ORD IDord-d4b94bacaba4414d98df07fcbcb409ba
Source noteuspto-grants-2014_11