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Synthesis and Characterization of 4-Phenyl Substituted 2-Aminothiazoles Coupling Intermediate for Organic Synthesis

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dc.contributor.author ISHEGBE, Joyce
dc.date.accessioned 2024-06-17T15:37:55Z
dc.date.available 2024-06-17T15:37:55Z
dc.date.issued 2020
dc.identifier.citation Synthesis and Characterization of 4-Phenyl Substituted 2-Aminothiazoles Coupling Intermediate for Organic Synthesis J. E. Ishegbe,* K. A. Bello, P. O. Nkeonye, A. A. Kogo en_US
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/2065
dc.description.abstract : A series of 4-aryl-2-aminothiazole were synthesized with an objective to develop novel and potent coupling components of synthetic origin as well as in dye synthesis. The required derivatives of 4-phenylsubstituted-2- aminothiazole were synthesized via a multicomponent condensation between thiourea, acetophenone and iodine. The intermediates were obtained using acetophenone and various substituted aldehydes to synthesize the intermediates which on cyclization with sulphur yielded the final products. Synthesized compounds were purified, characterized using UV-Visible Spectrophotometer, Infra–red, GC-MS Spectrometer and NMR. They were also evaluated for their spectra properties. All the synthesized intermediates exhibited moderate to significant properties. They were found to possess good coupling properties as well as high degree of brightness and a colour deepening effect compared to other heterocyclic couplers obtained from aniline and anthraquinone dyes. en_US
dc.language.iso en en_US
dc.publisher Ariviyal publishing en_US
dc.subject : 4-Phenyl-2-aminothiazole; green synthesis; acetophenone; heterocyclic compounds; spectral analysis en_US
dc.title Synthesis and Characterization of 4-Phenyl Substituted 2-Aminothiazoles Coupling Intermediate for Organic Synthesis en_US
dc.type Article en_US


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