Home|Journals|Articles by Year|Audio Abstracts
 

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

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






Full-text options


Share this Article


Online Article Submission
• ejmanager.com




ejPort - eJManager.com
Refer & Earn
JournalList
About BiblioMed
License Information
Terms & Conditions
Privacy Policy
Contact Us

The articles in Bibliomed are open access articles licensed under Creative Commons Attribution 4.0 International License (CC BY), which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.