A Literature Review on the Imidazole

 

MuhammedAbdel Hasan Shallal

M.ScinChemistry , Assist .Lecturer ,Thiqar Government ,Iraq

 

 

Abstract

This reviewgivessomeinformationaboutimidazoleringas a ( ligand , complex , antimicrobial , antimalarial , anticancer , uses , applications , linked�� withactivegroupssuchasSchiffbase , azogroup , ..).

 

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 thatmanyimidazole derivatives weredissolved in dilutedacid , andcoupling reaction(46) hours at (0) 0Cto give final product .

Couplingreaction that containing compounds react withandaromaticprimaryamineto produceimidazole- azodyes (47).These compounds have wide attention�� becauseoftheirpharmacological activities such as hypertensive agents (48),anticholinergic agents (49),antispasmodics(50), anticancer agents(51), oxo-tremorine antagonists (52) and antibacterial agents (53).

Otherpaper(54): synthesizedazo dyes- linkedwithphenolderivative�� fromcouplingreaction�� with different�� compoundsin presence ofdilutedhydrochloricacidto�� yieldligandsthencomplexationwithsomeions :

 

On the other hand , otherpaper(55)reportedthat imidazole � mannichderivatives(56)wereprepared through reaction ofsecondaryaromatic�� aminecompound withcarbonylcompound��� in presence ofstrong�� base, this mixture was stirredfor (5) hourstoformationmany�� antibacterialcompounds :

Whilestudying(57) usedbis- carboxylicacid and diaminecompounds�� inclosureconditions�� underrefluxingfor (6) hrs, then basified to giveimidazole derivative�� asanti- HIV :

 

Butinpaper(58) reacted the imidazolewith triazole in existence of ��closure�� conditions in DMF and stirred for (16 ) hours at room temperaturethenrefluxing�� for (7 ) hrs to give final productantifungalcompounds:

On the other hand�� researcher(59) addedimidazoleringtosulfur�� andnitrogencompounds�� toformationcompoundsinvolving�� antitumoractivities:

Innewpaper60) reported the preparation ofimidazole�� -azowithsulphonecompounds�� asantimlariacompounds:

 

Antmalariacompounds(61)was yield from reaction ofimidazolecompoundwithactiveringfromthiadiazoleoroxadiazolering:

Butotherstudying(61)formattedhydrazo- imidazolederivativesasantifungalcompounds

 

Paper(62) succeed to�� formatimidazole � iminecompoundsfromsubstituted compound reacted withdifferent aldehydesunder reflux (4) hours.

Otherliterature (63):prepared azomethine �imidazoleas analgesic�� by reaction of aromaticaldehydes withamine�� imidazole :

Imidazolederivativewas�� prepared by�� reactionofbenzimidazole(64)withsulfurordisulfidecompounds�� toformationcorrosioninhibitorscompounds:

Studying(65):preparedpolymer (vinyl chloride) dissolved in dry tetrahydrofuran, in reaction with amine underreflux for (7) hours to give final products�� asa polymers.

Imidazolein MixedLigands, Complex �Mixed , whichpreparedfromcondensationreactionofdi aminecompounds withcarbonylcompounds(66) :

Alsoinotherstudying,imidazoleligandwasprepared�� fromsulphonederivative(67) :

Other�� imidazolecompoundswereprepared�� as�� drugsinmedicalfields(68):

Butinnewstudies,imidazolecompoundswereprepared�� asantitumor�� inmedicinalfields(69-70):

Andother�� paper ,antibacterial(71-73)sulphonamide��� compoundswere synthesized:

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