Believes versus evidence-based regio-orientation in the structure assignment of pyrazolo[1,5-a]pyrimidines
Loading...
Date
2019-11
Journal Title
Journal ISSN
Volume Title
Publisher
Open Science Publishers LLP
Abstract
This review aims to focus and highlight the regio-orientation and regioselectivity of the reactions of 3(5)-aminopyrazoleswith 1,3-bielectrophilic reagents that lead to the formation of pyrazolo[1,5-a]pyrimidines. To clarify the significance ofregio-orientation, reactions of 3(5)-aminopyrazoles with symmetric 1,3-bielectrophilic reagents such as acetylacetoneand malononitrile are also included. The comparable nucleophilicity of the exocyclic NH2 group and endocyclicNH in 3(5)-aminopyrazoles is considered as it causes literature controversy associated with regio-orientation of thesubstituents on the pyrimidine ring of pyrazolo[1,5-a]pyrimidine when unsymmetrical 1,3-bielectrophilic reagentreacts with 3(5)-aminopyrazole. To the best of our knowledge, this review would be the first collective and confinedreport to the regio-orientation of pyrazolo[1,5-a]pyrimidines.
Description
Keywords
Regio-orientation, regioselectivity, 3(5)-Aminopyrazoles, pyrazolo[1,5-a]pyrimidines, 1,3-bielectrophilic reagents, symmetrical, unsymmetrical, exocyclic NH2, endocyclic NH.
Citation
Mohamed Mosaad Sayed, Mahmoud Asmaa Mahmoud. Believes versus evidence-based regio-orientation in the structure assignment of pyrazolo[1,5-a]pyrimidines. Journal of Applied Pharmaceutical Science. 2019 Nov; 2019 Nov: 126-144