A new synthetic route to 7H-imidazo[1,2-b][1,2,4]triazoles

Authors
Lee, KJSong, DHKim, DJPark, SW
Issue Date
1997-01
Publisher
Heterocorporation
Citation
Journal of Heterocyclic Chemistry, v.34, no.71, pp.71 - 76
Abstract
The reaction of benzil 1-ureidoethylidene hydrazones 8 with a mixture of triphenylphosphine, carbon tetrachloride, and triethylamine provides a general route to 7H-imidazo[1,2-b][1,2,4]triazoles 18 via the thermal reaction of the expected keto azine carbodiimide intermediates 13, and the structure of 18 was confirmed by X-ray crystallographic analysis.
Keywords
1,2,4-TRIAZOLE FUSED HETEROCYCLES; DERIVATIVES; 4H-1,2,4-TRIAZOLO<1,5-C><1,3,5>OXADIAZINES; REARRANGEMENT; AZINES; 7H-imidazo[1; 2-b][1; 2; 4]triazoles
ISSN
0022-152X
URI
https://pubs.kist.re.kr/handle/201004/144146
DOI
10.1002/jhet.5570340112
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KIST Article > Others
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