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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632201Generated: October 30, 2026

Ammonia → 2-Amino-1-carbethoxycarbonylmethyl-3-chloroquinoxalinium bromide

https://huagongshe.com/reaction/1632201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2,3-DichloroquinoxalineHCID 16659—
ReactantEthyl bromopyruvateHCID 66144—
Reactant3-Chloroquinoxalin-2-amineHCID 817274—
SolventEthanolHCID 702—
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 2,3-dichloro-quinoxaline and ammonia in ethanol by method of Saikachi et al (Chem. Pharm. Bull. Tokyo (1961), Vol. 9, p. 941], 12 g of ethyl bromopyruvate and 180 ml of dimethoxy ethane was stirred overnight and was filtered to obtain 5.33 of 2-amino-1-carbethoxycarbonylmethyl-3-chloro-quinoxalinium bromide in the form of a pale yellow crystalline solid. The filtrate was held in a refrigerator for 2 days to obtain 2 more crops of 1.20 and 3.62 g of product for a total yield of 10.22 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474784
Source datasetuspto-grants-1984_10
ORD IDord-0572298f1fd24cb6b1e676d4ccd0d99b
Source noteuspto-grants-1984_10