Abstract:
The work presented in this thesis involves the synthesis, characterization and
antimicrobial studies of carbazoles. Carbazoles, both isolated and synthesized, are
privileged heterocyclic compound that are dowered with exclusive properties as
photoelectric material, florescent agent, dyes and have tremendous role in medicinal
chemistry as antitumor, antimicrobial, antihistaminic, antineoplastic, antioxidative,
anti-inflammatory, anti HIV agent etc. Carbazole nucleus has been stimulating the
researchers to find new pathways for its synthesis and its novel derivatives because of
their extensive biological properties especially their amazing pharmacological profile
and their role as an emerging antibiotic. The current thesis work was designed based
on the documented facts highlighting the incredible applications of carbazole
derivatives in the field of chemistry. The work undertaken in this project was divided
in two sections. The first portion of section I focuses on synthesis of some known
potential carbazole derivatives (140-144 and 146-148) by adopting novel and feasible
synthetic protocols affording comparably effective yield. While the second portion
presents synthesis of some new carbazole derivatives with efficient synthetic
protocols and novelty. Novel carbazoles (149-151) were synthesized and among these
compounds 151 was found very reactive towards different functional which strongly
assist its further role in design and development progress of carbazoles. 151 was
further derivatized to successfully synthesize other novel carbazole derivatives such
as 151-157, 163-164, 166-170. All the synthesized compounds were characterized
from their spectral analysis i.e., UV, IR, 1 HNMR and mass spectrometry.
Having succeeded in attempt to synthesize carbazoles, these compounds were
evaluated and discussed for their antibacterial and anti-fungal activities in section II.
For the purpose of primary screening by agar well diffusion method reference strains
(ATCC) of three microbes Multi resistant staphylococcus aureus (gram positive
bacteria), Salmonella typhi (gram negative bacteria) and Candida albicans (fungi)
were used and then the minimum inhibitory concentration of each of the synthesized
compounds to kill these pathogens was found by agar dilution assay using different
clinical isolates of all three microbes. Synthesized carbazoles showed significant
activities against the tested microbes ranging from 50mg/mL to 2μg/mL. Thesevii
synthesized compounds were having potential to serve as important leads to fight
against drug resistant microbes among biologically active carbazoles.
O
O
N
O
N
NH
N
HN
N
H
NH
O
N
H
O
151
O
170
O
O
N
N
MeO
N
NH
N
H
OMe
166
Some synthesized novel carbazoles