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Original Article

ECB. 2015; 4(9): 436-441


SYNTHESIS OF NEW MERCAPTOPYRIMIDINES AND THIENOPYRIMIDINES

Abdelreheem A. Saddik, Khairy M. Hassan, Adel M. Kamal El-Dean, Mohamed S. Abbady.



Abstract
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2-Alkylmercapto- 4-Chloro-6-phenyl-pyrimidine-5-carbonitrile (4a-c) were synthesized and converted into 2-alkylmercapto 4-mercapto-6-
phenyl-pyrimidine-5-carbonitriles (7a-c). Compounds (7a-b) were alkylated with halogenated compounds to afford compounds (8a-g).
Compounds (8a-g) underwent Thorpe-Ziegler Cyclization to give thienopyrimidines (9a-g). 5-Amino-2-alkylmercapto-4-phenyl-thieno-
[2,3-d]pyrimidine-6-carboxamide derivatives (9a-f) underwent cyclization reaction using triethyl orthoformate to afford pyrimidothienopyrimidines (10a-e).

Key words: benzaldehyde, thiourea, ethyl cyanoacetate, α-halo carbonyl compounds





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