27182-39-4

Upstream product

• 28740-63-8 5-methyl-3-phenyl-1,3,4-oxadiazol-2(3H)-one 
• 75-44-5 phosgene 
• 2719-13-3 N'-(4-Nitro-phenyl)-N-acetyl-hydrazin 
• 14606-04-3 4-bromo-3-(4-nitrophenyl)-1,2,3λ⁵-oxadiazol-3-ylium-5-olate 
• 108-24-7 acetic anhydride 
• 6299-51-0 3-(4-nitrophenyl)sydnone 

Downstream Products

• 894423-32-6 C₉H₉N₅O₃ 
• 1449770-55-1 2-(4-nitrophenyl)-5-methyl-4-(1H-tetrazol-1-yl)-2H-1,2,4-triazol-3(4H)-one 
• 2719-13-3 N'-(4-Nitro-phenyl)-N-acetyl-hydrazin 

Relevant academic research and scientific papers

Zinc triflate catalyzed facile synthesis of novel 1,2,4-triazolinone derivatives using 3-Arylsydnone as synthon

A series of novel tetrazoles (4a-k) and thiazolidinones (6a-k) appended to 2-Aryl-1,2,4-triazolin-3-ones were efficiently synthesized from 3-Arylsydnones (1a-k) in excellent yields using Zinc triflate as catalyst.

Transformation of the sydnone ring into oxadiazolinones. A convenient one-pot synthesis of 3-aryl-5-methyl-1,3,4-oxadiazolin-2-ones from 3- arylsydnones and their antimicrobial activity

3-Arylsydnones (Ia-u) have been converted into the corresponding 3-aryl- 5-methyl-1,3,4-oxadiazolin-2-ones (IIIa-u) by a single-step reaction with bromine in acetic anhydride. In the preliminary screening of all these compounds, the halogen-substituted de