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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391822Generated: October 26, 2026

Water → 8-(2,6-Dichloro-3,5-dimethoxy-phenyl)-2-[(2-dimethylamino-ethyl)-methyl-amino]-quinoxaline-5-carboxylic acid

https://huagongshe.com/reaction/2391822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant8-(2,6-Dichloro-3,5-dimethoxy-phenyl)-2-[(2-dimethylamino-ethyl)-methyl-amino]-quinoxaline-5-carbonitrileHCID 59292938—
SolventEthylene GlycolHCID 174—
SolventDiethylether waterHCID 21584184—
Product8-(2,6-Dichloro-3,5-dimethoxy-phenyl)-2-[(2-dimethylamino-ethyl)-methyl-amino]-quinoxaline-5-carboxylic acidHCID 86641142—

Reaction Conditions

Temperature150 °C

Reaction Steps

A solution of KOH (268 mg, 4.79 mmol, 10 equiv) in H2O (2 mL) was added to 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-2-[(2-dimethylamino-ethyl)-methyl-amino]-quinoxaline-5-carbonitrile (Step 85.2) (220 mg, 0.48 mmol) in ethylene glycol (2 mL). The reaction mixture was stirred at 150° C. for 48 h, allowed to cool to rt, diluted with Et2O/H2O, and extracted with Et2O. The aqueous phase was acidified to pH 5 by addition of 6 N HCl. Vacuum filtration of the resulting suspension afforded 450 mg of the title compound as an impure yellow solid, which was used without further purification: ESI-MS: 479.0/480.9 [M+H]+; tR=3.75 min (System 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273882B2
Source datasetuspto-grants-2012_09
ORD IDord-553644d2a7ef42d18acc1c1ac2cc03fb
Source noteuspto-grants-2012_09