Cyclization Reactions of 5-Aminopyrazoles with β-Ketoesters, Enamines and β-Keto Anilides: New Synthetic Routes to Pyrazolo[1,5-a]Pyrimidine Derivatives
作者:F. M. A. El-Taweel、T. M. Abu Elmaati
DOI:10.1002/jccs.200200151
日期:2002.12
The pyrazolo[1,5-a]pyrimidines 4, 10, 11 and 14 were synthesized from reaction of 4-aryazo-2,5-diaminopyrazoles 1 with cyclic β-ketoesters 2a,b or cyclic β-ketoesters 7, 8 or acetoacetanilide 12, respectively. The reaction of 1 with the enamines 15, 16 and 17 yielded also the pyrazolo[1,5-a]pyrimidines 18, 20 and 21, respectively.
Selected compounds are effective for prophylaxis and treatment of inflammation and inflammatory disorders, such as NIK-mediated disorders. The invention encompasses novel compounds, analogs, prodrugs and pharmaceutically acceptable salts thereof, pharmaceutical compositions and methods for prophylaxis and treatment of diseases and other maladies or conditions involving, inflammation and the like.