Synthesis and Biological Evaluation of Pyrido(2,3-d)pyrimidines

被引:14
作者
Yousif, Mahmoud N. M. [1 ]
El-Gazzar, Abdel-Rahman B. A. [1 ]
El-Enany, Mervat M. [2 ]
机构
[1] Natl Res Ctr, Photochem Dept, Cairo, Egypt
[2] Cairo Univ, Fac Pharm, Pharmaceut Organ Chem Dept, Cairo, Egypt
关键词
Anticancer activity; antimicrobial activity; preparation; pyridines; pyridopyrimidines; pyrimidines; DERIVATIVES; INHIBITORS; AGENTS; ACID; 6-AMINO-2-THIOURACIL; PYRIMIDINE;
D O I
10.2174/1570193X17999200511010402
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
There are four types of pyridopyrimidines namely pyrido[2,3-d], pyrido[3,4-d], pyrido[4,3-d]pyrimidines, and pyrido[3,2-d]pyrimidines. Different methods of preparation of pyrido[2,3-d]pyrimidines are summarized. Synthesis of pyrido[2,3-d]pyrimidines can be from pyrimidines derivatives or pyridine derivatives. We can start from pyrimidine derivatives and build a pyridine ring. 5,7-Diphenylpyrido[2,3-d]pyrimidines 3 and 4 were obtained by the reaction of 6-aminouracil (1) with alpha,beta-unsaturated ketone. 6-Amino-1,3-dimethyluracil 10 was reacted with an equimolar amount of Mannich bases 11a-c under an atmosphere of nitrogen to give pyridopyrimidines 14a-c via the formation of the intermediates 12a-c& 13a-c. 4-Benzylamino derivative 19 could be converted to pyrido[2,3-d]pyrimidine derivative 20 by the reaction with dimethylformamide/ dimethylacetal. In the same way, we can start from pyridine derivatives and build a pyrimidine ring. Different reported biological activities of pyrido[2,3-d]pyrimidines are discussed e.g. selective adenosine kinase inhibitors, analgesic, anti-inflammatory, antimicrobial and herbicides, selective inhibitor of the tyrosine kinase activities of the fibroblast growth factor (FGF) and vascular endothelial growth factor (VEGF) receptors.
引用
收藏
页码:43 / 54
页数:12
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