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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43104Generated: October 30, 2026

Water → 8-(2,6-Dichloro-3,5-dimethoxyphenyl)-3-[(4-ethyl-1-piperazinyl)methyl]-5-quinoxalinecarboxylic acid

https://huagongshe.com/reaction/43104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 59292888HCID 59292888—
ReactantHCID 59292890HCID 59292890—
SolventEthylene GlycolHCID 174—
Product8-(2,6-Dichloro-3,5-dimethoxyphenyl)-3-[(4-ethyl-1-piperazinyl)methyl]-5-quinoxalinecarboxylic acidHCID 59292956—

Reaction Conditions

Temperature150 °C

Reaction Steps

A solution of KOH (0.818 g, 14.6 mmol, 10 equiv) in H2O (20 mL) was added to 710 mg (1.46 equiv) of a mixture of 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-3-(4-ethyl-piperazin-1-ylmethyl)quinoxaline-5-carbonitrile and 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-2-(4-ethyl-piperazin-1-ylmethyl)-quinoxaline-5-carbonitrile (Step 82.2) (710 mg, 1.46 mmol) in ethylene glycol (20 mL). The reaction mixture was stirred at 150° C. for 3 h, allowed to cool to rt and washed with EtOAc (2×100 mL). The aqueous layer was acidified to pH 3-4 by addition of 1N HCl. The resulting suspension was filtered. The filtrate contains 8-(2,6-dichloro-3,5-dimethoxy-phenyl)-2-(4-ethyl-piperazin-1-ylmethyl)-quinoxaline-5-carboxylic acid (Step 83.1). The residue in the filter was triturated in 1N HCl (3 mL) and filtered. The filtrate was basified to pH 5 and extracted with DCM (2×100 mL). The organic layer was dried (Na2SO4), filtered and concentrated to afford 190 mg of the title compound as a white solid: ES-MS: 505.0/506.6 [M+H]+; tR=3.46 min (System 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536175B2
Source datasetuspto-grants-2013_09
ORD IDord-372bcb3be95548b28f55904b941fd4ac
Source noteuspto-grants-2013_09