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.
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Original Russian Text © I.V. Dyachenko, R.I. Vas’kevich, A.I. Vas’kevich, V.V. Polovinko, M.V. Vovk, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 3, pp. 431–438.
For communication XVI, see [1].
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Dyachenko, I.V., Vas’kevich, R.I., Vas’kevich, A.I. et al. Fused Pyrimidine Systems: XVII. Imidazo- and Pyrimidopyrido[3,2-d]pyrimidin-4(3H)-ones. Russ J Org Chem 54, 436–443 (2018). https://doi.org/10.1134/S1070428018030119
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DOI: https://doi.org/10.1134/S1070428018030119