13576-46-0

Upstream product

• 13148-65-7 2,5-dimethyl-1,3,4-oxadiazole 
• 62-53-3 aniline 
• 1068-57-1 acetic acid hydrazide 
• 103-84-4 Acetanilid 
• 58010-97-2 N-acetyl-N'-formyl-hydrazine 
• 637-53-6 thioacetanilide 
• 18871-66-4 N,N-dimethylacetamide dimethyl acetal 
• 1286211-01-5 C₈H₁₁N₃ 
• 108-24-7 acetic anhydride 

Downstream Products

• 41217-51-0 1,3,5-trimethyl-4-phenyl-[1,2,4]triazolium; iodide 
• 142506-28-3 (R,S)-3-((1-hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl)-5-methyl-4-phenyl-1,2,4-triazole 
• 142506-27-2 3-(2-hydroxy-2-methyl-1-propyl)-5-methyl-4-phenyl-1,2,4-triazole 
• 39753-99-6 3-ethyl-5-methyl-4-phenyl-1,2,4-triazole 

Relevant academic research and scientific papers

HClO4-SiO2: An efficient reusable catalyst for the synthesis of 3,4,5-trisubstituted 1,2,4-triazoles under solvent-free conditions

A series of 3,4,5-trisubstituted 1,2,4-triazoles have been synthesized from N3-substituted amidrazones and anhydrides using HClO 4-SiO2 at 80 °C under solvent-free conditions. The products were obtained in excellent yields

Microwave-assisted synthesis of substituted 1,2,4-triazoles

An efficient synthesis of substituted 1,2,4-triazoles has been extended, utilising a wide range of N-substituted amides and hydrazides.

Efficient and regiospecific one-pot synthesis of substituted 1,2,4-triazoles

(Equation Presented) An efficient one-pot, three-component synthesis of substituted 1,2,4-triazoles has been developed, utilizing a wide range of substituted primary amines and acyl hydrazides.

THE SYNTHESIS OF SPIROCYCLIC TRIAZOLOQUINOLINES AS POTENTIAL LIGANDS FOR THE BENZODIAZEPINE RECEPTOR

Two spirocyclic triazoloquinolines (1a and b) have been prepared as potential ligands for the benzodiazepine receptor.Both compounds were prepared using the strategy of doubly deprotonating an acetanilide derivative followed by reaction with