1795-78-4

Usage

Chemical class

quinoxalinone

Biological activities

antitumor, antimicrobial, and anti-inflammatory properties

Uses

scientific research (potential therapeutic applications), building block in the synthesis of other organic compounds for pharmaceutical and medicinal purposes

Unique properties

phenyl group and a methoxy group attached to the quinoxalinone ring, which contributes to its potential pharmacological activities.

Upstream product

• 536-74-3 phenylacetylene 
• 102-51-2 4-methoxy-1,2-phenylenediamine 

Relevant academic research and scientific papers

Visible-light-induced, copper(i)-catalysed C-N coupling between o-phenylenediamine and terminal alkynes: One-pot synthesis of 3-phenyl-2-hydroxy-quinoxalines

Visible-light-initiated aerobic direct C-N coupling between o-phenylenediamines and terminal acetylenes was performed using simple copper(i) chloride as a catalyst for the synthesis of quinoxaline derivatives. The current method works well for a wide range of electron rich as well as electron poor group-substituted o-phenylenediamines and phenylacetylenes. The key component in the reaction is the direct photo-excitation of in situ generated copper arylacetylide (λabs = 420-480 nm). Moreover, as compared to the literature reports (thermal process), the current photochemical method is simple, mild, high yielding, and more viable towards the construction of biologically important quinoxaline derivatives from easily accessible raw materials, without the need of ligands and strong oxidants.