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Microwaves in organic synthesis: Facile synthesis of biologically active pyridazinone and iminopyridazine derivatives

✍ Scribed by Nadia Ragab Mohamed; Manal Mohamed Talaat El-Saidi; Yasser Mahmoud Ali; Mohamed Hilmy Elnagdi


Publisher
Journal of Heterocyclic Chemistry
Year
2007
Tongue
English
Weight
301 KB
Volume
44
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

magnified image

Condensation of Wittig reagents 1a,b with arylhydrazones 2a,b by conventional and by microwave heating techniques furnished the corresponding pyridazines 3a‐e. The arylhydrazones 7a,b were allowed to react with 1a,b under the same conditions to produce the pyridazinones 10a,b and iminopyridazines 11a,b respectively. On the other hand, the arylhydrazones 12a‐c reacted with 1a to afford the pyridazinones 13a‐c. Treatment of 3b with dimethylformamide dimethyl acetal (DMFDMA) produced the adduct 15. The utility of microwave heating technique led to the reduction of the reaction times to few minutes and to the improvement of the yields of the products. The in vitro biological activity of some newly prepared compounds against four types of fungi was studied.


πŸ“œ SIMILAR VOLUMES


Microwaves in organic synthesis: Synthes
✍ Balkis Al-Saleh; Morsy Ahmed El-Apasery; Noha M. Hilmy; Mohamed H. Elnagdi πŸ“‚ Article πŸ“… 2006 πŸ› Journal of Heterocyclic Chemistry 🌐 English βš– 375 KB

## Abstract magnified image The phenylhydrazones **1a‐d** condensed with ethyl cyanoacetate to yield pyridazinones **2a‐d** that reacted with sulphur in presence of piperidine to yield the aminothienopyridazineones **3a,b** that reacted with electron poor olefins and acetylenes to yield phthalazin