Synthesis and biological Evaluation of Some Abbreviated New pyrimidine derivatives

Authors

  • Jatin Vora  Department of Chemistry, Sheth L. H. Science College, Mansa, India (Scholars of Gujarat University, Ahmedabad), Gujarat, India
  • Kartik Vyas  Department of Chemistry, Sheth L. H. Science College, Mansa, Gujarat, India

DOI:

https://doi.org//10.32628/IJSRST1207250

Keywords:

(E)-1-(3,5-bis(trifluoromethyl)phenyl)-3-(substituted phenyl)prop-2-en-1-one, Urea, KOH and Ethanol.

Abstract

A cogent synthesis of completely new compound series of by  6-(3,5-bis(trifluoromethyl)phenyl)-4-(4-chlorophenyl)-3,4-dihydro pyrimidine-2(1H)-one    (Biginelli reaction) was achieved by continue heating of (E)-1-(3,5-bis(trifluoromethyl)phenyl)-3-(substituted phenyl)prop-2-en-1-one and urea for 5 hours with 40% KOH and ethyl alcohol. (E)-1-(3,5-bis(trifluoromethyl)phenyl)-3-(substituted phenyl)prop-2-en-1-one is produced by Claisen-Schmidt Condensation. In this condensation 1-(3,5-bis(trifluoromethyl)phenyl)ethanone and different aldehyde are mixed. All the novel compound series were characterized by infrared and 1H nuclear magnetic resonance and mass spectroscopic techniques and by elemental analyses. The newly synthesized compounds were evaluated for their antibacterial and antifungal activity

References

  1. Biginelli, P. (1891). "Ueber Aldehyduramide des Acetessigäthers". Chemische Berichte, 24: 1317–1319. doi:10.1002/cber.189102401228.
  2. Song, Dailei; Wang, Runxia; Chen, Yongli; Zhang, Shaohua; Liu, Chunsheng; Luo, Genxiang (2008). "Copper(II) trifluoroacetate catalyzed synthesis of 3,4-dihydropyrimidin-2(1H)-ones under solvent-free conditions". Reaction Kinetics and Catalysis Letters. 95 (2).
  3. Rovnyak, G. C.; Atwal, K. S.; Hedberg, A.; Kimball, S. D.; Moreland, S.; Gougoutas, J. Z.; O'Reilly, B. C.; Schwartz, J.; Malley, M. F. (1992). & quot; Dihydropyrimidine calcium channel blockers. 4. Basic 3-substituted-4-aryl-1,4-dihydropyrimidine-5-carboxylic acid esters. Potent antihypertensive agents & quot;. J. Med. Chem. 35 (17): 3254–3263.
  4. Reilly, B. C.; Atwal, K. S. (1987). & quot; Synthesis of Substituted 1,2,3,4-Tetrahydro-6-methyl-2-thioxo-5-pyrimidinecarboxylic Acid Esters & quot Heterocycles. 26 (5): 1189–1192. doi:10.3987/R-1987-05-1189.
  5. Kumar, Atul; Maurya, Ram Awatar (2007). "An efficient bakers' yeast catalysed synthesis of 3,4-dihydropyrimidin-2-(1H)-ones". Tetrahedron Letters. 48 (26): 4569.
  6. Chetan K Jadhav, Amol S Nipate, Asha V Chate, Vishal D Songire, Anil P Patil, Charansingh H Gill (2019) Efficient Rapid Access to Biginelli for the Multicomponent Synthesis of 1,2,3,4-Tetrahydropyrimidines in Room-Temperature Diisopropyl Ethyl Ammonium Acetate, ACS Omega December 31, 4 (27): 22313-22324.
  7. Shuyan Yu, Jingxin Wu, Hongbing Lan, Lihong Gao, Hengyu Qian, Kaiqi Fan, Zhigang Yin, “palladium and Bronsted acid co-catalyzed biginelli-like multicomponent reactions via in situ generated cyclic enol ether : Access tospirofuran- hydropyrimidines. Organic Letters 2019 December 18.
  8. National Committee for Clinical and Laboratory Standards, Method for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically Approved Standard, fourth ed. NCCLS, Villanova, Italy, Document M 100-S7, S100-S157 (1997).
  9. D.H. Isenberg, Essential Procedure for Clinical Microbiology, American Society for Microbiology, Washington, (1998).
  10. J. R. Zgoda, J. R. Porter, Pharm. Biol., 39, 221-225 (2001).

Downloads

Published

2019-05-30

Issue

Section

Research Articles

How to Cite

[1]
Jatin Vora, Kartik Vyas, " Synthesis and biological Evaluation of Some Abbreviated New pyrimidine derivatives, International Journal of Scientific Research in Science and Technology(IJSRST), Online ISSN : 2395-602X, Print ISSN : 2395-6011, Volume 6, Issue 3, pp.354-361, May-June-2019. Available at doi : https://doi.org/10.32628/IJSRST1207250