Ketones smoothly reacted with NBS in the presence of a catalytic amount of p-toluenesulfonic acid to give α-bromoketones in good yields in typical ionic liquids, such as [bmim]PF6 and [bmpy]Tf2N, and the ionic liquids could be repeatedly used for the same reaction after the extraction of the α-bromoketones. Then, the one-pot conversion of ketones into thiazoles by the treatment with NBS, and su...

Appearance and expansion of microbial resistance is one of the serious concerns in public health throughout the world. Thiazoles exhibits broad range of biological activities and was found in many active biological molecules. So far, it has proven that modifications of the thiazole ring are very effective with improved potency and less toxicity so that more than 90 % of novel drugs have the het...

A Simple and convenient protocol is described for preparation of some new 5-(2’hydroxy-3’,5’-dichlorophenyl)-4-(4’-chlorobenzyl)-2-amino-1,3-thiazole and 5-(2’hydroxy-3’,5’-dichlorophenyl)-4-(4’-chlorobenzyl)-2-aminophenyl-1,3-thiazole, were synthesized by refluxing dibrominated chalcone with thiourea or N-phenyl thiourea in good yields. The newly synthesized titled compounds were screened for ...

BACKGROUND Pyrazolo[1,5-a]pyrimidines are purine analogues. They have beneficial properties as antimetabolites in purine biochemical reactions. This division compounds have attracted wide pharmaceutical interest because of their antitrypanosomal activity. RESULTS The present work depicts an effective synthesis convention of pyrazolo[1,5-a]pyrimidines, pyrazolo[5,1-c]triazines, thieno[2,3-b]py...

Thiazolo[5,4-d]thiazoles are valuable materials for a range of technical and biological applications. They used as chemosensors, electroluminescent materials, organic light-emitting diodes (OLEDs), in solar cells, live-cell imaging, etc., those applications π-extended thiazolo[5,4-d]thiazole derivatives particularly attractive. A convenient synthetic route to non-symmetrical thiazolo[5,4-d]thia...

In the search for new fluorescent triphenylamine (TP) derivatives, we studied influence of position and substitution diverse heterocyclic substituents. A library 10 triphenylamines bearing either oxazoles or thiazoles pyridiniums, substituted at different positions has been developed. The approach is based on a convergent C−H activation reaction between pyridine-oxazoles pyridine-thiazoles di-i...

The reactivity of 2-deoxy-2-iodoglycosyl isothiocyanates toward O- and S-nucleophiles gives an easy access to 2-deoxy-2-iodoglycopyranosyl thiocarbamates and dithiocarbamates. Internal nucleophilic displacement of the iodine by the sulfur atom in these compounds allows the preparation of glycopyranoso[1,2-d]-1,3-thiazoles and glycopyranoso[1,2-d]-1,3-thiazolidin-2-one or -2-thione. Reaction wit...

Cyclocondensation of 2-[bis(methylthio)methylene]malononitrile (1) and cysteamine (2) afforded 2-(thiazolidin-2-ylidene)malononitrile (3). This compound on treatment with NaSH gave the corresponding thioamide derivative 4a in a regioselective manner on the basis of its single crystal X-ray diffraction analysis. Reaction of this compound with several alpha-bromocarbonyl compounds gave new 2-(E)-...

Reactions of 5-phenyl-3(3H)-thioxo-1,2,4-dithiazole (1) with unsaturated and active phosphonium salts as well as with phosphonates, at r. t. and under the effect of basic catalysis, afforded mainly 1,3,5dithiazines 5, 12, 17a, 17b, 23a or 23b. Substituted 1,3-dithiol 7 and 1,3-thiazoles 13, 19a, 19b, 22a and 22b were isolated as by-products. 1,3,5-Dithiazine products showed pharmacological pote...

Novel imidazo[2,1-b]thiazoles were synthesized in good yield via a mild reaction of thiophenytoin and diethyl oxalatein the presence of 10% mol p-TSA.