Synthesis of Some New Thiazolo Pyrimidines Using Cyclocondensation Reaction
Corresponding Author(s) : M. Amrollahi
akbar_mobini@yahoo.com
Asian Journal of Chemistry,
Vol. 17 No. 2 (2005): Vol 17 Issue 2
Abstract
Reaction of pyrimidine derivative 1 with chloroacetyl chloride under reflux condition in dioxane afforded fused pyrimidines 2(a-d). In a similar way fused thiazolo pyrimidine compounds 3(a-f) were synthesized by reaction of 1, chloroacetic acid, acetic anhydride, acetic acid and corresponding aldehyde. Yields of the products following recrystallizaton from ethanol were of the order of 66-93%. IR, 1H NMR and mass spectroscopies and in some cases elemental analysis were used for identification of these compounds.
Keywords
Pyrimidine
Thiazolo
Carboxylate
Biginelli Reaction
Methylketone
Amrollahi, M., Mobinikhaledi, A., & Forughifar, N. (2016). Synthesis of Some New Thiazolo Pyrimidines Using Cyclocondensation Reaction. Asian Journal of Chemistry, 17(2), 902–906. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/14276
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