Synthesis of spiro(pyrrol-2,5'-pyrrolo[2,3-d]pyrimidine)2',4',5,6'-tetraones by the reaction of pyrrolo[2,1-c][1,4]oxazinetriones with 6-aminopyrimidine-2,4-diones

Cover Page

Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription Access

Abstract

8-Aroyl-3,4-dihydro-1 H -pyrrolo[2,1- c ][1,4]oxazine-1,6,7-triones react with 6-aminopyrimidine-2,4(1 H ,3 H )diones to form 3-aroyl-4-hydroxy-1-(2-hydroxyalkyl)spiro(pyrrole-2,5'-pyrrolo[2,3- d ]pyrimidine)2',4',5,6'(1 H ,1' H ,3' H ,7' H )-tetraones, the structure of which was confirmed by X-ray diffraction analysis.

About the authors

N. A Tretyakov

Perm State University

Email: koh2@psu.ru

M. V Dmitriev

Perm State University

Email: koh2@psu.ru

A. N Maslivets

Perm State University

Email: koh2@psu.ru

References

  1. Денисламова Е.С., Банникова Ю.Н., Масливец А.Н. ЖОрХ. 2009, 45, 1272-1273.
  2. Denislamova E.S., Bannikova Yu.N., Maslivets A.N. Russ. J. Org. Chem. 2009, 45, 1264-1265. doi: 10.1134/S1070428009080302
  3. Денисламова Е.С., Бубнов Н.В., Масливец А.Н. ЖОрХ. 2011, 47, 915-918.
  4. Denislamova E.S., Bubnov N.V., Maslivets A.N. Russ. J. Org. Chem. 2011, 47, 933-936. doi: 10.1134/S1070428011060170
  5. Силайчев П.С., Масливец А.Н. ЖОрХ. 2013, 49, 958-959.
  6. Silaichev P.S., Maslivets A.N. Russ. J. Org. Chem. 2013, 49, 945-946. doi: 10.1134/S1070428013060298
  7. ElKalyoubi S., Fayed E. J. Chem. Res. 2016, 40, 771-776. doi: 10.3184/174751916X14798125870610
  8. Mohammadizadeh M.R., Azizian J., Teimouri F., Mohammadi A.A., Karimi A.R., Tamari E. Can. J. Chem. 2008, 86, 925-929. doi: 10.1139/V08-117
  9. Dabiri M., Azimi S.C., Khavasi H.R., Bazgir A. Tetrahedron. 2008, 64, 7307-7311. doi: 10.1016/j.tet.2008.05.063
  10. Ghahremanzadeh R., Azimi S.C., Gholami N., Bazgir A. Chem. Pharm. Bull. 2008, 56, 1617-1620. doi: 10.1248/cpb.56.1617
  11. Baradarani M.M., Farshi H., Khodaie M., Fazlelahi H.Z., Rashidi A., Joulec J.A. J. Heterocycl. Chem. 2017, 55, 91-96. doi: 10.1002/jhet.3008
  12. Spek A.L. Acta Crystallogr., Sect. C. 2015, 71, 9-18. doi: 10.1107/S2053229614024929
  13. CrysAlisPro, Agilent Technologies, Version 1.171.37.33 (release 27-03-2014 CrysAlis171.NET).
  14. Sheldrick G.M. Acta Crystallogr., Sect. A. 2008, 64, 112-122. doi: 10.1107/S0108767307043930
  15. Sheldrick G.M. Acta Crystallogr., Sect. A. 2015, 71, 3-8. doi: 10.1107/S2053273314026370
  16. Sheldrick G.M. Acta Crystallogr., Sect. C. 2015, 71, 3-8. doi: 10.1107/S2053229614024218
  17. Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. J. Appl. Crystallogr. 2009, 42, 339. doi: 10.1107/S0021889808042726
  18. Третьяков Н.А., Шаврина Т.В., Масливец А.Н. ЖОрХ. 2019, 55, 791-793.
  19. Tretyakov N.A., Shavrina T.V., Maslivets A.N. Russ. J. Org. Chem. 2019, 55, 719-720. doi: 10.1134/S1070428019050221

Supplementary files

Supplementary Files
Action
1. JATS XML
Download

Copyright (c) 2023 Russian Academy of Sciences