| Literature DB >> 23610964 |
Nehal A Hamdy1, Waled M El-Senousy.
Abstract
The enaminone 2 was reacted with hydrazonyl halides 3a-d to afford the corresponding pyrazole derivatives (6a-d) which reacted with hydrazine hydrate to afford the new pyrazolo[3,4-d]pyridazine derivatives 7a-d, respectively. In addition, compound 2 was reacted with some primary aromatic amines to afford the corresponding secondary enaminones 10a-c and reacted with sulfapyridine or sulfapyrimidine to afford the corresponding sulfonamide derivatives 12a and 12b. Evaluation of these new compounds against rotavirus Wa strain and adenovirus type 7 showed promising antiviral activity.Entities:
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Year: 2013 PMID: 23610964
Source DB: PubMed Journal: Acta Pol Pharm ISSN: 0001-6837 Impact factor: 0.330