Synthesis of 1-substituted [1,2,3]triazolo[4,5-d]pyridazines as precursorsfor novel tetraazapentalene derivatives

Citation
Kcv. Ramanaiah et al., Synthesis of 1-substituted [1,2,3]triazolo[4,5-d]pyridazines as precursorsfor novel tetraazapentalene derivatives, J HETERO CH, 37(6), 2000, pp. 1597-1602
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF HETEROCYCLIC CHEMISTRY
ISSN journal
0022152X → ACNP
Volume
37
Issue
6
Year of publication
2000
Pages
1597 - 1602
Database
ISI
SICI code
0022-152X(200011/12)37:6<1597:SO1[AP>2.0.ZU;2-O
Abstract
A series of 1-substituted 4,5-diformyl-[1,2,3]triazole derivatives were pre pared by 1,3-dipolar cycloaddition of aryl azides with acetylene dicarboxal dehyde mono-diethylacetal. The triazoles were readily converted into 1-subs tituted [1,2,3]triazolo[4,5-6]pyridazines in good yields. The 1-(2-nitrophe nyl)-[1,2,3]triazolo[4,5-d]pyridazine was found to be a useful intermediate for the generation of the novel SH-benzo[1,2,3]triazolo[1',2':1,2]triazolo [4,5-d]pyridazin-6-ium inner salt ring system.