Imidazole is a planar, five membered heteroaromatic molecule with pyrrole type and pyridine type annular nitrogens. Several approaches are available of imidazoles from alpha halo ketones, aminonitrile, aldehyde ect. Reactivity of imidazole and benzimidazole is referred from sets of resonance structure in which the dipolar contributors have finite importance. Imidazoles among the principal groups of heterocyclic compounds that have biological properties. Due to the presence of imidazole rings in natural products and active pharmaceutical ingredients, different ways for the synthesis of heterocyclic compounds of this type investigated. The aim of this project is substituted derivatives 2,4,5-Imidazoles. In this study, three-substituted imidazole compounds synthesized using ammonium chloride as a catalyst cost in terms of reflux were studied. Reaction with aldehydes and ammonium acetate Acenaphthene quinone in crowding conditions in the presence of ammonium chloride was performed successfully and imidazole derivatives were prepared with good yields. The key advantages of this process are high yields,cost effectiveness of catalyst,easy work-up and purification of products by non-chromatographic method. Manuscript profile

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New pyrimido [4, 5-e] [1, 3, 4]thia- diazin-7-yl] hydrazines were synthesized via the cyclocondensation of alkyl-2-phenylhydrazinecarbodithioates as a binucleophile with 5-bromo-2,4-dichloro-6-methylpyrimidine as a bielectrophile , and replacement of C-7 chloro atom by hydrazine in ethanol as the solvent . This method has advantages over methods currently described in the literature for the construction of such heterocyclic ring systems. Manuscript profile

In This applicable research, investigating absorption of process ofErythrosine dye on Copper oxide Nano particles Adsorbent was studied. First, prepared dyeconcentrations of 6, 8 and 12 mg L-1 and then effects of parameters such as concentrations ofinitial dye, time and pH on dye absorption efficiency were investigated.The dyeconcentrations in different samples were measured via spectrophotometer (505.6 nm for dyeErythrosine wavelength).The results of absorption studies showed that Erythrosine absorption or removal rateswould increase with decreasing the primary dye concentration, increasing reaction time , anddecreasing pH on the basis of the results, copper oxide Nano particles can the absorbErythrosine dye appropriately and efficiency of the process is higher in acidic pH for dyeErythrosine. The maximum dye removal of 93.68 % could be achieved at initial pH 2 usingadsorbent dosage of 0.233gr in 50 ml (12 mg L-1 dye concentration) and agitation rate of 180rpm. Effect of different parameters as kinetic parameters, were calculated pseudo-First andsecond-order kinetic, the Langmuir and Freundlich models Isotherm for absorb of this dye onadsorbent. this results showed that second-order kinetic adherence possessing regressioncoefficient of R2 ≥ 0.999, absorption or removal of Erythrosine on Copper oxide nanoparticles and different parameters for investigating of process rate of absorption in to be thisexperience. Equilibrium data fitted well with the Langmuir model for dye with adsorbent. Manuscript profile

TiO2 nanoparticles/melamine Tri sulfonic acid (MTSA) supported on silica gel as an efficient catalytic system for simple, one pot, solvent-free and environmentally benign process for synthesis of dihydropyrimidines via Biginelli reaction at 110 °C is described. It was found that the catalyst is reusable and exhibited remarkable activity. The catalyst can be easily separated and reused several times without appreciable loss of activity. The availability and recoverability of the catalytic system with easy operation and work up make this catalytic system attractive for organic synthesis. Manuscript profile

New 1,5-tetra alkyl methyl- phenyl-1H-pyrimido[4,5-e][1,3,4]thiadiazine-3,7-diamine were synthesized via the cyclocondensation of 2-(5-bromo-2-chloro-6-methylpyrimidin-4-yl)-2-methylhydrazine with phenylthioisothiocyanate and further replacement of chlorine atom on the seven number position of pyrimido[4, 5- e][1, 3, 4]thiadiazin by appropriate secondary amines in simple and efficient methods. Manuscript profile

Tripropylammonium fluorochromate(VI) (TPAFC), is an efficient and new reagent, which isprepared easily and oxidizes thiols to the corresponding disulfides, quickly. The reactions areperformed cleanly and are controlled to stop at the disulfide stage, without over-oxidation andside products. Coupling of thiols to their corresponding disulfides, are studied in solution atroom temperature and in solution under microwave radiation. The easy procedure, simple workup,short reaction times, and excellent yields, are another advantages of this reagent. Manuscript profile