A convenient synthesis of 5-(1,2,4-oxadiazol-5-yl)pyrimidine-2,4(1H,3H)-diones

被引:7
|
作者
Jakubiec, Dominika [1 ]
Walczak, Krzysztof Z. [1 ]
机构
[1] Silesian Tech Univ, Dept Organ Chem Bioorgan Chem & Biotechnol, PL-44100 Gliwice, Poland
关键词
5-Cyanouracil; 1,3-Dipolar cycloaddition; Nitrite oxide; Imidoyl chloride; 5-Heteroaryluracil; ANTIVIRAL ACTIVITY; NUCLEOSIDES; ANALOGS; ISOXAZOLINE;
D O I
10.1016/j.tetlet.2011.10.033
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of 5-heteroaryl-substituted uracil derivatives is presented. The 1,3-dipolar cycloaddition reaction was applied for the construction of a heterocyclic ring. The nitrile oxides were obtained from the appropriate 4-substituted benzaldoximes using N-chlorosuccinimide (NCS) under basic conditions. [2+3] Cycloaddition of nitrile oxides with 5-cyanouracil as a dipolarophile gave the corresponding 5-(3-substituited-1,2,4-oxadiazol-5-yl)uracils in satisfactory yields under mild conditions. 5-Substituted uracils having an additional heterocyclic ring were obtained as a result of the [2+3] cycloaddition of 5-cyanouracil to nitrile oxides generated from thiophene-2-carbaldehyde and 5-formyluracil derivatives. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6890 / 6891
页数:2
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