Microwaves in organic synthesis: Facile synthesis of biologically active pyridazinone and iminopyridazine derivatives
β 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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β¦ 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 3aβe. 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 12aβc reacted with 1a to afford the pyridazinones 13aβc. 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.
π SIMILAR VOLUMES
## Abstract magnified image The phenylhydrazones **1aβd** condensed with ethyl cyanoacetate to yield pyridazinones **2aβd** 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