Push-pull systems based on 2,4,6-triaryl pyrimidines. 2,4-diaryl-6- and 2-aryl-4,6-bis{4-[(E)-2-arylvinyl]phenyl}pyrimidines

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Тек жазылушылар үшін

Аннотация

Previously undescribed 2,4,6-triarylpyrimidines were synthesized by condensation of benzamidine and 4-(methyl-, 4-butoxy)benzamidine hydrochlorides with ( E )-1,3-diaryl-2-propen-1-ones in alcohol in the presence of KOH. The latter were reacted with ( E )- N -(2-chlorophenyl)-1-arylmethanimines in the KOH/LiH/DMF system to give 2,4-diaryl-6- and 2-aryl-4,6-bis{4-[( E )-2-arylvinyl]phenyl}-pyrimidines.

Авторлар туралы

A. Harutyunyan

Russian-Armenian (Slavonic) University;Scientific Technological Center of Organic and Pharmaceutical Chemistry (STCOPHCH)

Email: harutyunyan.arthur@yahoo.com

M. Safaryan

Scientific Technological Center of Organic and Pharmaceutical Chemistry (STCOPHCH)

Email: harutyunyan.arthur@yahoo.com

S. Dilanyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry (STCOPHCH)

Email: harutyunyan.arthur@yahoo.com

H. Panosyan

Scientific Technological Center of Organic and Pharmaceutical Chemistry (STCOPHCH)

Email: harutyunyan.arthur@yahoo.com

G. Danagulyan

Russian-Armenian (Slavonic) University;Scientific Technological Center of Organic and Pharmaceutical Chemistry (STCOPHCH)

Email: harutyunyan.arthur@yahoo.com

Әдебиет тізімі

  1. Selivanova D.G., Gorbunov A.A., Mayorova O.A., Vasyanin A.N., Lunegov I.V., Shklyaeva E.V., Abashev G.G. Beilstein J. Org. Chem. 2017, 13, 1583-1595. doi: 10.3762/bjoc.13.158
  2. Verbitskiy E.V., Dinastiya E.M., Baranova A.A., Khokhlov K.O. Chuvashov R.D., Yakovleva Y.A., Makarova N.I., Vetrova E.V., Metelitsa A.V., Slepukhin P.A., Rusinov G.L., Chupakhin O.N., Charushin V.N. Dyes Pigm. 2018, 159, 35-44. doi: 10.1016/j.dyepig.2018.05.075
  3. Achelle S., Rodríguez-López J., Robin-le Guen F. ChemistrySelect. 2018, 3, 1852-1885. doi: 10.1002/slct.201702472
  4. Achelle S., Rodríguez-López J., Larbani M., Plaza-Pedroche R., Robin-le Guen F. Molecules. 2019, 24, 1742. doi: 10.3390/molecules24091742
  5. Harutyunyan A.A., Panosyan H.A., Ghukasyan G.T., Danagulyan G.G. Chem. J. Arm. 2018, 71, 634-637.
  6. Арутюнян А.А., Паносян Г.А., Сафарян М.С., Арутюнян Г.К., Гукасян Г.Т., Данагулян Г.Г. ЖОрХ. 2020, 56, 269-276.
  7. Harutyunyan A.A., Panosyan H.A., Safaryan M.S., Harutyunyan G.K., Gukasyan G.T., Danagulyan G.G. Russ. J. Org. Chem. 2020, 56, 269-275. doi: 10.1134/S1070428020020153
  8. Komatsu R., Sasabe H., Kido J. J. Photon. Energy. 2018, 8, 032108. doi: 10.1117/1.JPE.8.032108
  9. Ouyang Y., Li J., Chen X., Fu X., Sun S., Wu Q. Biomolecules. 2021, 11, 894. doi: 10.3390/biom11060894
  10. Tekale S., Mashele S., Pooe O., Thore S., Kendrekar P., Pawar R. Biological Role of Chalcones in Medicinal Chemistry. Vector-Borne Diseases - Recent Developments in Epidemiology and Control. Ed. D. Claborn. London: IntechOpen, 2020. doi: 10.5772/intechopen.91626
  11. Aldaghri O. Materials. 2021, 14, 2766. doi: 10.3390/ma14112766
  12. Bhat P., Shridhar G., Ladage S., Ravishankar L. J. Chem. Sci. 2017, 129, 1441-1448. doi: 10.1007/s12039-017-1327-x
  13. Jin J., Zhao Y., Sze E.M.L., Kothandaraman P., Chan P.W.H. Adv. Synth. Catal. 2018, 360, 4744-4753. doi: 10.1002/adsc.201801178
  14. Zhao J., Qiu J., Gou X., Hua C., Chen B. Chin. J. Catal. 2016, 37, 571-578. doi: 10.1016/S1872-2067(15)61043-9
  15. Арутюнян А.А., Паносян Г.А., Данагулян Г.Г. ЖОрХ. 2020, 56, 1748-1754.
  16. Harutyunyan A.A., Panosyan G.A., Danagulyan G.G. Russ. J. Org. Chem. 2020, 56, 1952-1957. doi: 10.1134/S1070428020110093
  17. Moreau M., Karadavidoff I. Пат. 2.301.160 (1973). ФРГ. С.А. 1973, 79, 126064y.
  18. Sint Org. Prep. 1949, 1, 75.
  19. Yoshifuji M., Nagase R., Kawashima T., Inamoto N. Bull. Chem. Soc. Jpn. 1982, 55, 870-872. doi: 10.1246/bcsj.55.870
  20. Bule M.H., Esfandyari R., Tafesse T.B., Amini M., Faramarzi M.A., Abdollahi M. J. Chem. Pharm. Res. 2019, 11, 27-37.

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML

© Russian Academy of Sciences, 2023