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International Letters of Chemistry, Physics and Astronomy
Volume 51

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An Expeditious Synthesis of 1,2,4-Triazolo[1,5-<i>a</i>]Pyrimidine
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An Expeditious Synthesis of 1,2,4-Triazolo[1,5-a]Pyrimidine

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Abstract:

A simple, efficient, and diversity oriented synthesis of library of 1,2,4-triazolo [1,5-a] pyrimidine was undertaken using 5-amino,1,2,4-triazole as a building block. The synthesized analogues were fully characterized by known spectroscopic techniques like FT-IR, 1H NMR, 13C NMR, and mass spectroscopy.

Info:

Periodical:
International Letters of Chemistry, Physics and Astronomy (Volume 51)
Pages:
1-4
DOI:
https://doi.org/10.18052/www.scipress.com/ILCPA.51.1
Citation:
A.M. Shah and A.J. Rojivadiya, "An Expeditious Synthesis of 1,2,4-Triazolo[1,5-a]Pyrimidine", International Letters of Chemistry, Physics and Astronomy, Vol. 51, pp. 1-4, 2015
Online since:
May 2015
Authors:
A.M. Shah, A.J. Rojivadiya
Keywords:
1,2,4-Triazolo[1,5-a]Pyrimidine, 5-Amino,1,2,4-Triazole, Diversity Oriented Synthesis, Spectroscopic Techniques
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Open Access

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This work is licensed under a
Creative Commons Attribution 4.0 International License

References:

[1] Syamala M., Org. Prep. Proced. Int. 41 (2009) 1.

[2] Syamala M., Org. Prep. Proced. Int. 37 (2005) 103.

[3] Fischer, G., Adv. Heterocyclic Chem. 57 (1993) 81.

[4] Shaban, M.A.E. Morgan, A.E.A., Adv. in Hetero. Chem. 77 (2000) 345.

[5] Shaban, M.A.E. Morgan, A.E.A. Adv. in Hetero. Chem., 73 (2000) 131.

[6] Shaban, M.A.E. Morgan, A.E.A. Adv. in Hetero. Chem, 75, (2000 ) 243.

[7] Zhang, N. Semiramis, A. K. J. Med. Chem., 50 (2007) 319.

[8] Havlicek, L. Fuksova, K. Krystof, V. Bioorg. And Med. Chem. 13 (2005) 5399.

[9] Fraley M. E., Hoffman W. F. Rubino R. S. Bioorg. And Med. Chem. Lett. 12 (2002) 2767.

[10] Chen, Q. Zhu, X. L. Liu, Z. M. Europ. J. Med. Chem. 43 (2008) 595.

[11] Shaabani A., Farhangi E. Rahmati A., Comb. Chem. 9 (2006) 771.

[12] Heravi M. M., Derikvand F. Ranjbar L., Synth. Commun., 40 (2010) 677.

[13] Lipson V. V., Desenko S. M., Borodina V. V., Musatov V. I., Russ. J. Org. Chem. 41 (2005) 114.

[14] Shankar R. B. Pews R. G., J. Heterocycl. Chem. 30 (1993) 169.

[15] Fedorova O. V., Zhidovinova M. S., Rusinov G. L., Ovchinnikova I. G., Russ. Chem. Bull., Int. Ed. 52, (2003) 1768.

[16] Uryu, S., Tokuhiro, S., Murasugi, T., Brain Research 946 (2002) 298.

[17] Fairfield, B. J.; Andrew, C.; Allan, J. WO2004108136, (2004).

[18] Peng, H., Kumaravel, G., Yao, G., Sha, L., Wang, J., Van Vlijmen, H., Bohnert, T., Huang, C., Vu, C. B., Ensinger, C. L., Chang, H., Engber, T. M., Whalley, E. T., Petter, R. C., J. Med. Chem. 47 (2004) 6218.

DOI: https://doi.org/10.1021/jm0494321
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