Anal. calcd. for C18H21Cl2N3O: C, 59.02; H, 5.78; Cl, 19.36; N, 11.47; O, 4.37. Found: C, 59.15; H, 5.88; N, 11.56. The synthesis of (SLN1–SLN10) successfully synthesised by using good literature. Majorly we selected related drug candidates, prepared skeleton. Simple convergent methodology worked for getting good yields overall. The final C–N coupling approached three techniques, where we concluded Sonication technique is see more good for getting good yield and time. We observed more spots in microwave reaction may be due to microwave other bonds also dislocated and afford low yield. The same conventional reaction yield shown less and taking long time. The explosive reactions, like azide and Mitsunobu reactions etc.,

are not useful for bulk scale. We recommend for small scale reactions in Ultra-Sonication SCR7 purchase reactions and microwave reactions based on our earlier experience. All authors have none to declare. The authors acknowledge the Osmania University for providing the research facility and the direct contributions for the staff of Department of Chemistry and Analytical team. “
“Vildagliptin chemically (S)-1-[N-(3-hydroxy-1-adamantyl) glycyl] pyrrolidine-2-carbonitrile, is a potent dipeptidyl peptidase IV (dip-IV) inhibitor, a drug for the treatment of diabetes. DPP IV

inhibitors represent a new class of oral antihyperglycemic agents to treat patients with type 2 diabetes. DPP IV inhibitors improve fasting and postprandial glycemic control without hypoglycemia or weight gain. Vildagliptin inhibits the inactivation below of GLP-1 and GIP by DPP IV, allowing GLP-1 and GIP to potentiate the secretion of insulin in the beta cells and suppress glucagon release by the alpha cells of the islets of Langerhans in the pancreas. 1, 2, 3 and 4 Literature survey reveals that vildagliptin can be estimated by UV spectroscopic method, 5 RP-HPLC method, which is a time consuming method

being the retention time is more than 10 min, 6 RP-LC/MS method, requires mass spectroscopy detection and the LOD and LOQ are more than the present method, and has a narrow linearity range, 7 HPLC method, which requires a solid-phase extraction and determination by high-performance liquid chromatography quadrupole time-of-flight mass spectrometry which requires a special attention throughout the study but the present work is a simple method. 8 So based on the above mentioned reasons the authors aim to develop a simple, sensitive and accurate RP-HPLC method for the estimation of vildagliptin in pure form and tablet dosage form. Waters 2695 HPLC system equipped with Agilent Eclipse XDB C18, 150 × 4.6 mm, 5 μ column, Rheodyne injector with 25 μL loop, 2996 PDA detector and Empower-2 software was used. Potassium dihydrogen orthophosphate of analytical grade, HPLC grade Milli-Q water and acetonitrile were used. Vildagliptin was a gift sample from Novartis, India. The tablets of vildagliptin were obtained from local pharmacy. 0.