Synthesis and Anticonvulsive Activity of 7-Amino-Substituted Cyclopenta[4′,5′]-pyrido[3′,2′:4,5]furo[3,2-d]pyrimidines

被引:0
作者
S. N. Sirakanyan
A. A. Ovakimyan
A. S. Noravyan
I. A. Dzhagatspanyan
A. A. Shakhatuni
I. M. Nazaryan
A. G. Akopyan
机构
[1] National Academy of Sciences of the Republic of Armenia,Institute of Fine Organic Chemistry, Scientific
来源
Pharmaceutical Chemistry Journal | 2013年 / 47卷
关键词
furo[3,2-; ]pyrimidines; cyclopenta[; ]pyridines; synthesis; cyclization; amino derivatives; anticonvulsive activity;
D O I
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中图分类号
学科分类号
摘要
Methods for the synthesis of new cyclopenta[4′,5′]pyrido[3′,2′:4,5]furo[3,2-d]pyrimidine derivatives based on 3-oxo-derivatives of cyclopenta[c]pyridines were developed. O-alkylated derivatives of these latter compounds were cyclized to furo[2,3-b]pyridines, which were converted to furo[3,2-d]pyrimidin-7-ones with formamide. Subsequent chlorination and amination of 7-oxo derivatives yielded 7-amino derivatives. The anticonvulsive and predicted tranquillizer activities of the compounds synthesized here were assessed. Compounds with anticonvulsant properties were identified.
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页码:130 / 134
页数:4
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