A Literature Review on the Imidazole
Muhammed
Abdel Hasan Shallal
M.Sc in Chemistry , Assist .Lecturer ,Thiqar
Government ,Iraq
Abstract
This review gives
some information about imidazole ring
as a ( ligand , complex , antimicrobial , antimalarial , anticancer ,
uses , applications , linked with active
groups such as
Schiff base , azo group , ..).
Keywords: Uses, Applications
Imidazole ring has five membered ring systems that
contain hydrogen binding domain, and electron donor nitrogen system(1-3).The first imidazole was described by Fischer (1882),
but the nature of the ring system was demonstrated by Freud and Kuhn (1890)(4-6).
Imidazole
are important because their biological activity among their
isomer, particularly the imidazole possessed a broad spectrum of biological
activities including antimicrobial (90)antituberculosis(7-11)
antioxidant(12-16) anti-inflammatory(17-20) anticonvulsants(21-25)
antidepressant and anxiolytic(26-31) antihypertensive(32-36)
anticancer(37-40) and antifungal activity(41-44).
Also, studying(45) reported thatmany imidazole
derivatives were dissolved in diluted acid , and
coupling reaction(46) hours at (0) 0Cto
give final product .
Coupling reaction that containing compounds react
with and
aromatic primary amine
to produce imidazole- azo dyes (47).These compounds have
wide attention because of
their pharmacological activities
such as hypertensive agents (48),anticholinergic agents (49),antispasmodics(50),
anticancer agents(51), oxo-tremorine antagonists (52) and
antibacterial agents (53).
Other paper(54): synthesizedazo dyes- linked
with phenol derivative
from coupling reaction
with different compounds in presence of diluted
hydrochloric acid to
yield ligands then
complexation with some
ions :
On the other
hand , other paper(55) reported that imidazole – mannich derivatives(56)were prepared through reaction
of secondary aromatic
amine compound with carbonyl
compound in presence of strong
base, this mixture was stirred
for (5) hours to formation
many antibacterial compounds :
While studying(57)
usedbis- carboxylic acid and
diamine compounds in
closure conditions under
refluxing for (6) hrs, then
basified to give imidazole
derivative as anti- HIV :
But in
paper(58) reacted the imidazolewith triazole in existence of closure
conditions in DMF and stirred
for (16 ) hours at room temperature
then refluxing for (7 ) hrs to give final product antifungal
compounds:
On
the other hand researcher(59) addedimidazole
ring to sulfur
and nitrogen compounds
to formation compounds
involving antitumor activities:
In new
paper60) reported the preparation ofimidazole -azo
with sulphone compounds
as antimlaria compounds:
Antmalaria compounds(61)was
yield from reaction of imidazole compound
with active ring
from thiadiazole or
oxadiazole ring :
But other studying(61) formatted hydrazo- imidazole derivatives
as antifungal compounds
Paper(62) succeed to format
imidazole – imine compounds fromsubstituted
compound reacted with different
aldehydes under reflux (4) hours.
Other literature (63):prepared azomethine –imidazole as analgesic
by reaction of aromatic aldehydes
with amine imidazole :
Imidazole derivative
was prepared by reaction
of benzimidazole(64)with sulfur
or disulfide compounds
to formation corrosion
inhibitors compounds:
Studying(65): prepared polymer (vinyl chloride) dissolved in dry
tetrahydrofuran, in reaction with amine under
reflux for (7) hours to give final products as a
polymers.
Imidazole in Mixed
Ligands , Complex –Mixed ,
which prepared from
condensation reaction of di
amine compounds with carbonyl
compounds(66) :
Also in other
studying , imidazole
ligand was prepared
from sulphone derivative(67) :
Other imidazole compounds
were prepared as
drugs in medical
fields(68):
But in new
studies, imidazole compounds
were prepared as
antitumor in medicinal
fields(69-70):
And other paper ,
antibacterial(71-73)sulphonamide compounds
were synthesized:
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