Ethyl {4-[2-(saccharin-2-yl)acetylsulfamoyl]phenylazo}cyanoacetate in the synthesis of polyfunctionally heteroaromatic derivatives
β Scribed by A. A. Aly
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2009
- Tongue
- English
- Weight
- 122 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.176
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β¦ Synopsis
Abstract
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An efficient and direct oneβpot reaction of ethyl saccharinylcyanoacetate derivative 3 with a variety of active methylene reagents and nitrogen nucleophiles afforded novel series of polyfunctionally substituted heteroaromatic derivatives 5β13, respectively. The pyrazole derivative 13 was seemed to be the excellent precursors for the synthesis of pyrazolo[1,5βa]pyrimidine derivatives 14β24. The antimicrobial screening of some synthesized products was evaluated against some selected bacteria and fungi. The structures of the synthesized derivatives were established by elemental and spectral data. J. Heterocyclic Chem., (2009).
π SIMILAR VOLUMES
## Abstract __N__β[4β(Dicyanomethylazo)phenyl]β2βsaccharinβ2βylacetamide (**__2__**) proved to be a convenient precursor for the synthesis of a variety of pyridazine and pyrimidine derivatives **__4a,b,6__**, and **__7__**. Also a series of substituted pyrimidines **__10β16__** were prepared from t