Firstly in this article, two series compounds ofN-(4-Hydroxy-4-methyl-3-aryl-thiazolidin-2-yl)-ferrocenylamide andN-(4-Hydroxy-4-phenyl-3-aryl-thiazolidin-2-yl)-ferrocenylamide weresynthesized from unsymmetric ferrocenyl thiourea derivatives, which wereformed by ferrocenyl formyl-acid.Secondary, benzimidazole derivatives were prepared by the reaction ofiodobenzene diacetate with N, N'-diphenylbenzamidine at room temperature.Finally, the compounds N-acetylbenzamide (5a~5j) andN-(5-oxo-5H-1,2,4-dithiazol-3-yl)arylamide 6 were formed by the reaction ofthe IBD with benzoyl isothiocyanate.The structures of compounds were confirmed by 1H NMR, 13C NMR, MS,IR data. In addition, the structure of 2b and 6b was comfirmed by RigakuMercurry CCD X-ray imaging.
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