Abstract

Design, Synthesis and Biological Activity of Some Benzimidazoles Derivatives 3-Chloro-4-(Substituted--phenyl-1-(4-{1-[2'-(2H-tetrazol-5-yl)-biphenyl-4- ylmethyl]-1H-benzimidazol-2yl}-phenyl)-azetidin-2-ones

A novel method for the synthesis of novel 3-Chloro-4(4-chloro-phenyl-1-(4-{1-[2'-(2H-tetrazol- 5-yl)-biphenyl-4-ylmethyl]-1H-benzimidazol-2yl}-phenyl)-azetidin-2-one derivatives have been reported. Structures of all the synthesized compounds have been corroborated on the basis of elemental IR, 1H NMR, 13C NMR and Mass spectro-analytical data. Many Schiff bases were prepared by condensation reaction of nitro compound containing biphenyl tetrazole with aromatic aryl aldehydes derivatives with azetidin-2-one. The synthesized compounds were screened for AT1 Angiotension (A II) Receptor Antagonist activity. The nitro, chlorine, hydroxy, florine, iodo compound containing biphenyl tetrazole Schiff bases azetidin-2-one shows good activity compared with losartan and Telmisartan


Author(s): M. C. Sharma a, D. V. Kohli a, Smita Sharmab and A. D. Sharmac

Abstract | PDF

Share This Article
Awards Nomination 17+ Million Readerbase
Google Scholar citation report
Citations : 5682

Der Chemica Sinica received 5682 citations as per Google Scholar report

Der Chemica Sinica peer review process verified at publons
Abstracted/Indexed in
  • Google Scholar
  • Open J Gate
  • Genamics JournalSeek
  • China National Knowledge Infrastructure (CNKI)
  • Directory of Research Journal Indexing (DRJI)
  • Publons
  • MIAR
  • International Committee of Medical Journal Editors (ICMJE)
  • Serials Union Catalogue (SUNCAT)
  • Geneva Foundation for Medical Education and Research
  • Secret Search Engine Labs
  • Euro Pub
  • CAS (Chemical Abstracting Services)
  • University of Barcelona

View More »

Flyer image
T�rkiye'nin Yeni Nesil Bahis Adresi Matadorbet giris Adresi G�ncellenmistir!