A series of novel 10-phenylsulfonyl-2-substituted-4,10 dihydrobenzo[4,5]imidazo[1,2-a]pyrimidin-4-one derivatives obtained from N-sulfonation of 2-substituted-pyrimido[1,2-a]benzimidazol-4(10H)-ones and screened for for their in vitro anti-tuberculosis activities against Mycobacterium tuberculosis H37Rv by Microplate Alamar Blue Assay (MABA) method. The structures were established on the basis of their IR, ¹H-NMR, ¹³C-NMR, ESI-MS data and also the compound with 3f were crystallized and analysed by single crystal X-ray diffraction studies.

An ionic liquid 1-Butyl-3-methylimidazoliumchloride[BMIm]Cl/sodium hydroxide system, was employed as a catalyst for the fast and one-pot crossed aldol-condensation of various aromatic aldehydes and cyclic ketones, to produce a variety of substituted ?,? & apos; -bis(benzylidene)-cycloalkanones under neat conditions. This process is simple, efficient and environmentally benign and proceeds in high yield and short reaction times. The ionic liquid can be recycled for subsequent reactions without any appreciable loss of efficiency.

The synthesis of Triphenylphosphonium trichloroiodoaluminate (III) ionic liquids (ILs) is reported here. The product was characterized by spectroscopic and analytical methods such as 31P-NMR, FT-IR, cyclic voltammetry, CHN, TGA and differential thermal analysis (DTA). Thermal analyses were used to investigate the thermal behavior of this compound. The results show that this ILs has excellent thermal stability below 110?C. Along with the experimental study; this compound has been studied computationally at the B3LYP/LANL2DZ level of theory using the Gaussian 98 program package. From these calculations, optimized geometries, molecular parameters, and vibrational spectra of ILs have been calculated. In addition, calculated frequencies are compared with the experimental frequencies after correction by the appropriate scaling factor. This comparison shows that our theoretical data are in good agreement with the experimental results.

An efficient and practical, three-component one-pot condensation reaction between 1, 2-phenylenediamine, 2-mercaptoacetic acid and aromatic aldehydes in ionic liquids have been reported for the synthesis of 1-aryl-1H, 3H-thiazolo [3, 4-a] benzimidazoles derivatives in excellent yields.