Studies on potential antitubercular agents. Synthesis of 1-(2′-morpholino-3′-quinoxalinoyl)-2-benzalhydrazine and 2-aryl-3-(2′-morpholino-3′-quinoxalimido)-4-thiazolidinones was written by Fernandes, P. S.;Sonar, T. M.. And the article was included in Journal of the Indian Chemical Society in 1988.Recommanded Product: 49679-45-0 This article mentions the following:
Quinoxalinecarboxylic acid benzylidenehydrazides underwent cycloaddition-cyclocondensation with HSCH2CO2H to give thiazolidinones I [R1 = Ph, thienyl, HOC6H6, O2NC6H4, ClC6H4, (MeO)3C6H2, HO(MeO)C6H3]. Some I showed antitubercular activity. In the experiment, the researchers used many compounds, for example, Ethyl 3-chloroquinoxaline-2-carboxylate (cas: 49679-45-0Recommanded Product: 49679-45-0).
Ethyl 3-chloroquinoxaline-2-carboxylate (cas: 49679-45-0) belongs to quinoxaline derivatives. Condensed heterocycles of quinoxalines have become attractive targets in synthetic and medicinal chemistry due to their significant biological activities. The antitumoral properties of quinoxaline compounds have been of interest. Recently, quinoxaline and its analogs have been investigated as the catalyst’s ligands.Recommanded Product: 49679-45-0
Referemce:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider