Novel One-Pot Synthesis Of Thiazolo[3,2-A] Pyrimidin-5-One As A Key Compound For Poly Nuclear Heterocycles
EGYPTIAN JOURNAL OF CHEMISTRY(2016)
Abstract
3-AMINO-2-hydroxy-7-methyl-thiazolo[3,2-a] pyrimidin-5-one (5) was synthesized by one-pot reaction from 2-bromo cyanoacetamide, ethyl acetoacetate and thiourea. The new 3-amino-2-hydrazino derivatives (15,18), 2-pyrazol-thiazolo [3,2-a] pyrimidin -5-ones) 14,17,20) and 2-(4-arylidene) -pyrazol-thiazolo [3,2-a] pyrimidin-5-ones (22a-d) were synthesized through facile condensing procedures starting from 3-amino-2-hydrazino-7-methyl-thiazolo[3,2-a]pyrimidin-5-one (12). The newly synthesized products were characterized by their IR, ESI-MS, NMR and micro analytical data.
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Key words
Thiazolo [3,2-a] pyrimidin-5-one, One pot synthesis, Condensation, Intramolecular Cyclization and Tautomerism
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