Convenient synthesis of some new thiazolidin-4-one, chromen-2-imine and pyrrol-2-one derivatives containing thiophene moiety | ||
Mansoura Journal of Chemistry | ||
Volume 46, Issue 4, December 2019, Pages 7-11 PDF (908.67 K) | ||
Document Type: Original Article | ||
DOI: 10.21608/mjcc.2019.413044 | ||
Authors | ||
Ahmed Mekabaty* 1; A. S . Fouda2; Ibrahim E . I. Shaaban2 | ||
1Chemistry Department, Faculty of Science, Mansoura University | ||
2Chemistry Department, Faculty of Science, Mansoura University, El-Gomhoria Street, ET-35516 Mansoura, Egypt | ||
Abstract | ||
In the present study, 2-amino-4-methyl-5-(pyridin-2-ylcarbamoyl)thiophene-3-ethylcarboxylate (2) has been achieved using Gewald’s methodology between 3-oxo-N-(pyridin-2-yl)butanamide (1), ethyl 2-cyanoacetate and elemental sulfur in refluxing ethyl alcohol containing a catalytic amount of morpholine. This 2-aminothiophene derivative was served as key synthon for the synthesis of new thiazolidin-4-one, chromen-2-imine and pyrrol-2-one derivatives via its reactions with the convenient chemical reagents. The mechanistic aspects for the achievement of the new thiophene derivatives were also discussed | ||
Keywords | ||
Thiophene; thiazolidinone; chromene; pyrrolone; Gewald’s methodology | ||
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