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- DOI 10.18231/2394-2797.2018.0007
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Synthesis of novel pyridine containing azetidinone derivatives as a potential anti tubercular activity
- Author Details:
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N. Pramod
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B. Mayuri
Six novel pyridine containing azetidinones Azt 1-6 have been synthesized from Schiff base by treating Pyridine-4-carbaldehyde with Substituted aromatic amines each were taken equimolar concentration in presence of Glacial acetic acid as a catalyst using Grindstone technique. Further Schiff base add benzene, triethylamine and chloro acetyl chloride undergoes condensation followed by elimination reaction result into novel pyridine containing azetidinone derivatives. The newly synthesized derivatives were characterized by using spectroscopic methods (IR, 1H-NMR, MASS) and screened for selected anti-tubercular. In vitro anti-tubercular activity was performed using Micro plate Alamar Blue Assay (MABA) method. Among synthesized compounds Azt5 and azt6 showed more potent Anti TB activity than standards.
Keywords: Pyridine-4-carbaldehyde, Schiff base, Azetidinones, anti-tubercular activity.
References
- Sigma-Aldrich. Retrieved 28 November 2011.
- "Pyridine". Encyclopædia Britannica Online.
- Mootz, D. (1981). "Crystal structures of pyridine and pyridine trihydrate". The Journal of Chemical Physics. 75 (3):
- Bibcode:1981JChPh..75.1517M. doi:10.1063/1.442
[Google Scholar] - "Iodine Solution (0.02 M in THF/pyridine/H2O 70:20:10)". Sigma-Aldrich. Retrieved 28 November 2011.
- "Pyridine". Encyclopædia Britannica Online.
- IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Schiff base".
- Schiff, Hugo (1866). "Eine neue Reihe organischer Diamine. Zweite Abtheilung" [A new series of organic diamines. Second part.]. Annalen der Chemie und Pharmacie (in German). 140:92–137.
- IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "azomethines".
- IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "anils".
- Gilchrist, T. (1987). Heterocyclic Chemistry. Harlow: Longman Scientific. ISBN 0-582-01421-2.
- Brandt, C.; et al. (2017). "In silico serine β-lactamases analysis reveals a huge potential resistome in environmental and pathogenic species". SciRep. 7 (43232). Bibcode:2017NatSR...74323 2B. doi:10.1038/srep43232
[Google Scholar] - "Tuberculosis Fact sheet N°104". WHO. October
- Archived from the original on 23 August 2012. Retrieved 11 February 2016.
- The Chambers Dictionary. New Delhi: Allied Chambers India Ltd. 1998. p. 352. ISBN 978-81-86062-25-
- Archivedfrom the original on 6 September 2015.
- Dolin, [edited by] Gerald L. Mandell, John E. Bennett, Raphael (2010). Mandell, Douglas, and Bennett's principles and practice of infectious diseases (7th ed.). Philadelphia, PA: Churchill Livingstone/Elsevier. pp. Chapter 250. ISBN 978-0-443-06839-3
- Konstantinos A (2010). "Testing for tuberculosis". Australian Prescriber. 33 (1): 12–18. Archived from the original on 4 August 2010.
How to Cite This Article
Vancouver
Pramod N, Mayuri B. Synthesis of novel pyridine containing azetidinone derivatives as a potential anti tubercular activity [Internet]. Int J Pharm Chem Anal. 2018 [cited 2025 Oct 09];5(1):39-42. Available from: https://doi.org/10.18231/2394-2797.2018.0007
APA
Pramod, N., Mayuri, B. (2018). Synthesis of novel pyridine containing azetidinone derivatives as a potential anti tubercular activity. Int J Pharm Chem Anal, 5(1), 39-42. https://doi.org/10.18231/2394-2797.2018.0007
MLA
Pramod, N., Mayuri, B.. "Synthesis of novel pyridine containing azetidinone derivatives as a potential anti tubercular activity." Int J Pharm Chem Anal, vol. 5, no. 1, 2018, pp. 39-42. https://doi.org/10.18231/2394-2797.2018.0007
Chicago
Pramod, N., Mayuri, B.. "Synthesis of novel pyridine containing azetidinone derivatives as a potential anti tubercular activity." Int J Pharm Chem Anal 5, no. 1 (2018): 39-42. https://doi.org/10.18231/2394-2797.2018.0007