82450-99-5

Upstream product

• 2103-99-3 4-(4-chlorophenyl)-2-thiazolamine 
• 64310-34-5 3-(p-methylphenyl)-5-mercapto-4H-1,2,4-triazole 
• 87614-22-0 N-(4-p-chlorophenylthiazole-2-yl)p-tolylimidoyl chloride 
• 87614-01-5 2-p-methylbenzoylamino-4-p-chlorophenylthiazole 
• 874-60-2 4-methyl-benzoyl chloride 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 103966-18-3 1-(4-p-chlorophenylthiazol-2-yl)-5-p-tolyltetrazole 

Relevant academic research and scientific papers

Synthesis of 2,5-Diarylthiazolo-s-triazoles

2,5-Diarylthiazolo-s-triazoles (II) have been synthesised via 1-(4-arylthiazol-2-yl)-5-aryltetrazoles (VII).Compounds (VII) have been synthesised by the reaction of 2-aroylamino-4-arylthiazoles (V) with phosphorus pentachloride, and azidolysis of t

Heterocyclic Systems Containing Bridgehead Nitrogen Atoms: Part XLV - Reaction of 5-Mercapto-3-p-tolyl-s-triazole with α,β-Bifunctional Compounds

5-Mercapto-3-p-tolyl-s-triazole (II) on condensation with α-halogenoketones and subsequent cyclization of the intermediate ketones (III) with PPA furnishes the corresponding thiazolo-s-triazoles (IV) and not the isomeric thiazolo-s-triazoles

Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Syntheses of Thiazolo-s-triazoles & Isomeric Thiazolo-s-triazole

The reaction of 3-p-tolyl-5-mercapto-s-triazole (II) with α-haloketones in dry methanol gives thiazolo-s-triazole (III) derivatives in one-step and not the isomeric thiazolo-s-triazole (V) derivatives.Unequivocal synthesis of latter has also