STUDEIS ON THE SYNTHETIC POTENTIALITIES OF SOME CYANOACTAMIDE DERIVATIVES
Asmaa Mahmoud Fahim Abd Elwahed;
Abstract
Cyclohexylamine (14) reacts with ethyl cyanoacetate under solvent free condition to afford the 2-cyano-N-cyclohexylacetamide (16) (Chart 1).
When compound 16 was treated with aromatic aldehydes 17a-f, it afforded the novel acrylamide derivatives 18a-f. Treatment of compounds 18b with hydrazine hydrate and with phenylhydrazine gave the corresponding
aminopyrazole derivatives 20a and 20b, respectively. (Chart 1).
When compound 16 was treated with aromatic aldehydes 17a-f, it afforded the novel acrylamide derivatives 18a-f. Treatment of compounds 18b with hydrazine hydrate and with phenylhydrazine gave the corresponding
aminopyrazole derivatives 20a and 20b, respectively. (Chart 1).
Other data
| Title | STUDEIS ON THE SYNTHETIC POTENTIALITIES OF SOME CYANOACTAMIDE DERIVATIVES | Other Titles | " دراسات على الامكانات التخليقية لبعض مشتقات سيانواسيتاميد " | Authors | Asmaa Mahmoud Fahim Abd Elwahed | Issue Date | 2009 |
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