Abstract
The carbanions of ethylcyanoacetate, cyanoacetanilide, malononitrile and cyanoacetamide react with Aryl carbamoyl aryl hydrazidoyl cblorides (1 a-f) in ethanol at room temperaturc tc give the corresponding substituted pyrazoles (3a-f, 6a-c, 7a-e and 8a). The structural assignments have been made on the basis of elemental analysis, spectral data and the Chemical evidence fer the resulting pyrazoles. On the other hand, aminoacetonitrile was reacted with (1b) and 9 to give the corresponding substituted triazines (13b) and quinolino [1, 2-f) ] triazone derivative (12). The mechanism of the different reactions wcre discussed.
References
- Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
Abstract
References
- Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
Details
| Primary Language | English |
|---|---|
| Subjects | Chemical Engineering |
| Journal Section | Research Article |
| Authors | |
| Publication Date | January 1, 1985 |
| Published in Issue | Year 1985 Volume: 31 |
Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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