Fused Pyrimidine Systems: XVII. Imidazo- and Pyrimidopyrido[3,2-d]pyrimidin-4(3H)-ones
- Authors: Dyachenko I.V.1, Vas’kevich R.I.1, Vas’kevich A.I.2, Polovinko V.V.3, Vovk M.V.1
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Affiliations:
- Institute of Organic Chemistry
- “Igor Sikorsky Kyiv Polytechnic Institute” National Technical University of Ukraine
- “Enamin” Scientific Industrial Association
- Issue: Vol 54, No 3 (2018)
- Pages: 436-443
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/217325
- DOI: https://doi.org/10.1134/S1070428018030119
- ID: 217325
Cite item
Abstract
2-(Allylamino)pyrido[3,2-d]pyrimidin-4(3H)-one was converted to linearly fused dihydroimidazo- [1,2-a]pyrido[3,2-d]pyrimidine on heating in polyphosphoric acid, whereas its reactions with molecular iodine and chlorosulfanylarenes afforded mainly angularly fused analogs. 2-(Cinnamylamino)pyrido[3,2-d]pyrimidin- 4(3H)-one reacted with polyphosphoric acid and chlorosulfanylarenes to give linear pyrido[3,2-d]pyrimido-[1,2-a]pyrimidinones, and its iodocyclization led to the formation of angularly fused derivative.
About the authors
I. V. Dyachenko
Institute of Organic Chemistry
Author for correspondence.
Email: irina_chem@ukr.net
Ukraine, ul. Murmanskaya 5, Kiev, 02094
R. I. Vas’kevich
Institute of Organic Chemistry
Email: irina_chem@ukr.net
Ukraine, ul. Murmanskaya 5, Kiev, 02094
A. I. Vas’kevich
“Igor Sikorsky Kyiv Polytechnic Institute” National Technical University of Ukraine
Email: irina_chem@ukr.net
Ukraine, Pr. Peremohy 37, Kiev, 03056
V. V. Polovinko
“Enamin” Scientific Industrial Association
Email: irina_chem@ukr.net
Ukraine, Kiev
M. V. Vovk
Institute of Organic Chemistry
Email: irina_chem@ukr.net
Ukraine, ul. Murmanskaya 5, Kiev, 02094
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