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Original Article

ECB. 2014; 3(7): 713-718


SYNTHESIS OF THIENO[3,2-d]PYRIMIDIN-4-ONES AND ALKYLATION THEREOF

Alexander S. Shestakov, Mikhail A. Prezent, Victor G. Kartsev, Khidmet S. Shikhaliev.



Abstract
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The 3-R-thieno[3,2-d]pyrimidine-2,4(1H,3H)-diones (5a-с) and 3-R-2-thioxo-2,3-dihydrothieno[3,2-d]pyrimidine-4(1H)-ones (5d-g) were
synthesized using methyl 3-aminothiophene-2-carboxylate and alkyl-, arylisocyanates and isothiocyanates respectively, which in turn
converted into its N- и S- alkyl derivates (8a-e, 9a-g). 2-Aminothieno[3,2-d]pyrimidin-4(3H)-one (14a-c, 16) were received as a result the
interaction the methyl 3-aminothiophene-2-carboxylate with benzoyl- and pyrimidin-2-yl cyanamides.

Key words: thiophenes, thienopyrimidinones, 3-R-thieno[3,2-d]pyrimidine-2,4(1H,3H)-dione, 3-R-2-thioxo-2,3-dihydrothieno[3,2- d]pyrimidin-4(1H)-one, 2-aminothieno[3,2-d]pyrimidin-4(3H)-one, alkylation





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