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Regioselective synthesis of new 2-(E)-cyano(oxazolidin-2-ylidene)thiazolesDOI: 10.5155/eurjchem.2.3.356-358.389 Keywords: Thiazole , Oxazolidine , Hantzsch’s synthesis , Heterocyclization , Regioselective synthesis , Phosphorus pentasulfide Abstract: Reaction of 2-(oxazolidin-2-ylidene)malononitrile (1) with phosphorus pentasulfide gave the corresponding thioamide derivative (2a) in a regioselective manner. Reaction of this compound with several α-bromocarbonyl compounds gave new 2-(E)-cyano(oxazolidin-2-ylidene)thiazoles (3a-g). The chemical structures of novel compounds were confirmed by 1H NMR, elemental analysis, FT-IR spectrometry and mass spectrophotometric analyses.
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