1334597-65-7

Upstream product

• 35676-70-1 2-chloro-3-hydroxy-quinoxaline 
• 31595-63-8 2-hydroxy-3-hydrazinebenzopyrazine 
• 95-54-5 1,2-diamino-benzene 
• 15804-19-0 quinoxaline-2,3-dione 
• 163402-50-4 C₁₅H₁₂N₄O₂ 
• 79-04-9 chloroacetyl chloride 

Relevant academic research and scientific papers

Synthesis and antimicrobial activity of novel thiazolidinone and azetidinone derivatives

Reaction of 2,3-diketoquinoxaline in presence of phosphorus pentachloride and hydrazine hydrate gives 2-hydrazino-3-hydroxyquinoxalin (4) which on treatment with various aldehydes in appropriate solvent gives 2-p-anisyl-3-(3-hydroxy quinoxalin-2 yl-amino)-4-thiazolidinones (6) and 1-N-(3-hydroxy quinoxalin-2'yl-amino)-4-aryl-3-chloro-2-azetidinones (7). The structure of compounds 6a-6l and 7a-7l has been confirmed by IR and 1H NMR data. All these compounds were tested for their antimicrobial and antifungal activity against different microorganisms.