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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422227Generated: November 1, 2026

Triethylamine → N-(7-bromo-2,3-dimethoxy-quinoxalin-5-ylmethyl)-oxalamic acid ethyl ester

https://huagongshe.com/reaction/1422227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 18706309HCID 18706309—
ReactantOxalic acid monoethylester chlorideHCID 23618337—
SolventTetrahydrofuranHCID 8028—
ProductN-(7-bromo-2,3-dimethoxy-quinoxalin-5-ylmethyl)-oxalamic acid ethyl esterHCID 54297612—

Reaction Conditions

Temperature0 °C

Reaction Steps

300 mg (1 mmol) of 5-aminomethyl-7-bromo-2,3-dimethoxyquinoxaline hydrochloride are suspended in 10 ml of THF and the suspension is cooled to 0° C. 0.183 ml (1.3 equiv.) of triethylamine is added and then 0.123 ml (1.1 equiv.) of oxalic acid monoethyl ester chloride is added dropwise in the course of 30 minutes. The mixture is stirred at 0° C. for 2 hours, then at 20° C. for 16 hours and is concentrated by evaporation. The residue is stirred in diethyl ether, and the solid is filtered off, washed with water and diethyl ether and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080743
Source datasetuspto-grants-2000_06
ORD IDord-3a4eeae901ef4f8f8829ea663f2041ce
Source noteuspto-grants-2000_06