Azole heterocyclic compounds exhibit wide range of medicinal applications in the treatment of various types of diseases [1]. Especially, triazole derivatives as medicinal drugs have been playing important roles in medicinal chemistry [2-4], and a lot of triazole analogs including imidazole [5], thiazole [6], carbazole [7,8], oxazole [9] and benzimidazole [10,11], etc. have also been found to be...

A series of 1-(2-hydroxyethyl)-3,5-dimethylpyrazolylazo derivatives, incorporating thiosemicarbazide 2a-c, 1,3,4-thiadiazole 3a-c, and 1,2,4-triazole-3-thione 4a-c were synthesized. The structure of these novel synthesized compounds 2a-c, 3a-c, and 4a-c was confirmed by spectral analysis. All these compounds were screened for their analgesic activity. Hot-plate and tail-immersion tests were use...

Purpose: To synthesize new triazole derivatives in order to overcome the problem of side effects antimicrobial agents and microbial resistance, while broadening spectrum activity.
 Methods: The starting triazole, compound 1, was prepared through click chemistry reacted with chloroacetyl chloride yield II. Triazole 1 acids aldehydes produce oxadiazole (III) azomethine (IV) which cyclized ac...

epilepsy is the most frequnt nearological affiction and afflicts 1% about of the worlds population. currently there is an urgent need for the development of novel anticonvulsants with higher levels of potency and lower levels of toxicity. in this paper, a series of new 6-(substituted-phenyl)thiazolo[3,2-b][1,2,4]triazole derivatives were synthesized and tested for their anticonvulsant activity ...

Iminoester hydrochlorides 1 have been synthesized. These compounds were then converted into ester ethoxycarbonyl hydrazones 2, from which in turn a new series of substituted 4-amino-4,5-dihydro-1H-1,2,4-triazole-5-ones, 3, was then prepared. Finally a set of isatin imine derivatives 4 was obtained from the reaction of compounds 3 with isatin. The structures of all the new synthesized compounds ...

A facile synthetic method to access 3-substituted isoquinoline or dihydroisoquinoline derivatives has been developed via a novel cyclization reaction of N-sulfonyl-1,2,3-triazole derivatives by thermally induced rearrangement.

A method for the synthesis of N-aryl-C-nitroazoles is presented. A coupling reaction between variously substituted arylboronic acids and 3(5)-nitro-1H-pyrazole catalyzed by copper salt has been carried out in methanol in the presence of sodium hydroxide to afford the desired N-aryl-C-nitroazoles in good yields. This synthetic route has also been successfully applied to obtain N-phenyl derivativ...

3,4-diaryl-1,2,4-triazole-5-yl-propenoic acid derivatives as cis or trans isomers were tested for their antimicrobial activity.

A bioorthogonal 'catch and photorelease' strategy, which combines alkyne-azide cycloaddition between p-hydroxyphenacyl azide and alkyne derivatives to form a 1,2,3-triazole adduct and subsequent photochemical release of the triazole moiety via a photo-Favorskii rearrangement, is introduced. The first step can also involve photorelease of a strained alkyne and its Cu-free click reaction with azide.

Allene triazole derivatives were successfully synthesized for the first time through iron catalyzed regioselective triazole addition to tertiary propargyl alcohols. The reaction proceeds under mild conditions, giving the desired allene-triazoles in good to excellent yields (up to 96%). The resulting allene-triazoles were confirmed by X-ray crystallography and indicated improved stability.