Dergiler / Journal of Scientific Reports-A / 2022 / Sayı: 048

NEW SCHIFF BASES DERIVED from 3,4-DIAMINO-1H-1,2,4-TRIAZOLE-5(4H)-THIONE: SYNTHESIS and CHARACTERIZATION

Sayfa
25–41
Yayın Tarihi
2022-03-31
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The structures of the new compounds were characterized by spectral (IR, 1H and 13C NMR) and elemental analysis.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:A new synthetic approach has been applied to obtain a compound 3,4-diamino-1H-1,2,4-triazole-5(4H)-thione (2) by using 5-amino-1,3,4-thiadiazole-2-sulfonamide (1) and hydrazine hydrate as starting materials.
📊
Temel Bulgular & Veri:New Schiff bases (3a-d) are obtained by the reaction of the compound 3,4-diamino-1H-1,2,4-triazole-5(4H)-thione (2) and varied aldehydes.
💡
Sonuç & Katkı:The structures of the new compounds were characterized by spectral (IR, 1H and 13C NMR) and elemental analysis.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Thione · Schiff base · Sulfonamide

Abstract

A new synthetic approach has been applied to obtain a compound 3,4-diamino-1H-1,2,4-triazole-5(4H)-thione (2) by using 5-amino-1,3,4-thiadiazole-2-sulfonamide (1) and hydrazine hydrate as starting materials. New Schiff bases (3a-d) are obtained by the reaction of the compound 3,4-diamino-1H-1,2,4-triazole-5(4H)-thione (2) and varied aldehydes. The structures of the new compounds were characterized by spectral (IR, 1H and 13C NMR) and elemental analysis.

🔖

Bu Makaleye Atıf Yap

BÜYÜKKIDAN, B., BÜYÜKKIDAN, N., ATAR, A. (2022). NEW SCHIFF BASES DERIVED from 3,4-DIAMINO-1H-1,2,4-TRIAZOLE-5(4H)-THIONE: SYNTHESIS and CHARACTERIZATION. Journal of Scientific Reports-A, Sayı: 048, 25–41. https://ajindex.com/articles/778963

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (11)

  1. Klimeˇsova, V., Zahajka, L., Waisser, K., Kaustova, J., M¨ollmann, U., (2004), Synthesis and antimycobacterial activity of 1,2,4-triazole 3-benzylsulfanyl derivatives, Il Farmaco, 59, 279–288
  2. Zani, F., Vicini, P., Incerti, M., (2004), Synthesis and antimicrobial properties of 2-(benzylidene-amino)-benzo[d]isothiazol-3-ones, Eur. J. Med. Chem. 39, 135–40
  3. Tehranchian, S., Akbarzadeh, T., Fazeli, M. R., Jamalifar, H., Shafiee, A., (2005), Synthesis and antibacterial activity of 1-[1,2,4-triazol-3-yl] and 1-[1,3,4-thiadiazol-2-yl]-3-methylthio-6,7-dihydrobenzo[c]thiophen-4(5H)ones, Bioorg. Med. Chem. Lett. 15, 1023–1025
  4. Sahoo, S., Patwari, P. K., Kumar, M. C. B., Setty, C. M., (2013), Synthesis and Biological Activity of Certain Mannich Bases Derivatives from 1,2,4-Triazoles, Iranian J. Pharma. Sci., 9(4), 51–60
  5. Al-Khuzaie, M. G. A., Al-Majidi, S. M. H., (2014), Synthesis, Characterization and Evaluation Antimicrobial Activity of Some New substituted 2-Mercapto-3-Phenyl-4(3H)- Quinazolinone, Iraqi J. Sci., 55(2B), 582–593
  6. Mahmoud, M. R., Abou-Elmagd, W. S. I.,. El-Shahawi, M. M., Hekal, M. H., (2014), Novel Fused and Spiro Heterocyclic Compounds Derived from 4-(4-Amino-5-mercapto-4H1,2,4-triazol-3-yl)phthalazin-1(2H)-one, Eur. Chem. Bull., 3(7), 723–728
  7. Hanif, M., Saleem, M., Hussain, M. T., Rama, N. H., Zaib, S., Aslam, M. A. M., Jones, P. G., Iqbal, J., (2012), Synthesis, Urease Inhibition, Antioxidant and Antibacterial Studies of Some 4-Amino-5-aryl-3H-1,2,4-triazole-3- thiones and Their 3,6-Disubstituted 1,2,4-Triazolo[3,4- b]1,3,4-thiadiazole Derivatives, J. Braz. Chem. Soc., 23(5), 854–860
  8. Hope, W. W., Lewis, R., Smith, J. A., (2010), Clinical Primer: Potential Hepatic Complications with Triazole Therapy, USA: University of Wisconsin-Madison School of Medicine and Public Health, School of Pharmacy, and School of Nursing and Fallon Medica LLC
  9. Boraei, A. T. A., Singh, P. K., Sechi, M., Satta, S., (2019), Discovery of novel functionalized 1,2,4-triazoles as PARP-1 inhibitors in breast cancer: Design, synthesis and antitumor activity evaluation. Eur. J. Med. Chem., 182, 111621
  10. Arul, K., Smith, A. A., (2014), In-Silico Design, Synthesis and in vitro Anticancer Evaluation of Some Novel 1,2,4- Triazole Derivatives, The Experiment, 21(1), 1439–1452
  11. El-Sherief, H. A. M., Youssif, B. G. M., Abbas Bukhari, S. N., Abdelazeem, A. H., Abdel-Aziz, M., Abdel-Rahman, H. M., (2018), Synthesis, anticancer activity a