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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1578070Generated: October 31, 2026

Ethyl bromopyruvate → 2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromide

https://huagongshe.com/reaction/1578070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
Reactant3-Chloroquinoxalin-2-amineHCID 817274—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromideHCID 14067523—

Reaction Steps

A solution of 9 g of 2-amino-3-chloro-quinoxaline [prepared by heating under pressure in ethanol, ammonia and 2,3-dichlorquinoxaline as taught by Saikachi et al (Chem. Pharm. Bull. Tokyo (1961), Vol. 9, P. 94)], 12 g of ethyl bromopyruvate and 180 ml of dimethoxyethane was stirred overnight and was then vacuum filtered to recover 5.33 g of a pale yellow crystalline solid. The filtrate stood in the refrigerator for several days to recover 1.20g and 3.62 g of the same compound for a total yield of 10.22 g of 2-amino-1-carbethoxycarbonylmethyl-3-chloro-quinoxalinium bromide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04291033
Source datasetuspto-grants-1981_09
ORD IDord-e539911c83d8485bb0d8220ff14fb00d
Source noteuspto-grants-1981_09