2005
DOI: 10.1080/104265090508091
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Reactions with Hydrazonoyl Halides 421: Synthesis of Some New 2,3-Dihydro-1,3,4thiadiazoles, 2,3-Dihydro-1,3,4-selenadiazoles and Triazolino[, ]pyrimidines

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Cited by 17 publications
(2 citation statements)
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“…Treatment of 2‐(2‐phenylhydrazono)‐1‐(5‐bromobenzofuran‐2‐yl)‐2‐chloroethanone ( 4 ) with ethyl 4‐methyl‐6‐phenyl‐2‐thioxo‐1,3,6‐trihydropyrimidine‐5‐carboxylate ( 5a ) in chloroform and triethylamine gave ethyl 1,5‐dihydro‐3‐(5‐bromobenzofuran‐2‐oyl)‐7‐dimethyl‐1,5‐diphenyl‐[1,2,4]triazolo[4,3‐ a ]pyrimidine‐6‐carboxylate ( 9a ; Scheme ). The structure of 9a was elucidated on the basis of both elemental analysis and spectral data as well as alternative synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…Treatment of 2‐(2‐phenylhydrazono)‐1‐(5‐bromobenzofuran‐2‐yl)‐2‐chloroethanone ( 4 ) with ethyl 4‐methyl‐6‐phenyl‐2‐thioxo‐1,3,6‐trihydropyrimidine‐5‐carboxylate ( 5a ) in chloroform and triethylamine gave ethyl 1,5‐dihydro‐3‐(5‐bromobenzofuran‐2‐oyl)‐7‐dimethyl‐1,5‐diphenyl‐[1,2,4]triazolo[4,3‐ a ]pyrimidine‐6‐carboxylate ( 9a ; Scheme ). The structure of 9a was elucidated on the basis of both elemental analysis and spectral data as well as alternative synthesis.…”
Section: Resultsmentioning
confidence: 99%
“…23 1,3,4-Selenadiazoles have been prepared by the reaction of potassium selenocyanate with hydazonoyl bromide. 24 Oxidation of aryl selenoamides with N-bromosuccinimide and iodine yielded 1,2,4-selenadiazoles. 25 Some of the disadvantages such as basic conditions, longer reaction duration and low yields limit the applicability of these methods.…”
Section: Introductionmentioning
confidence: 99%