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REACTİON OF ARYL CARBAMOYL ARYL HYDRAZİDOYL CHLO- RIDES WITH ACTIVATED NITRILE

Year 1990, Volume: 36 , - , 01.01.1990
https://doi.org/10.1501/Commub_0000000450

Abstract

The carbanions of ethyl cyanoacetate, cyanoacetanilide, malononitrile and cyanoacetami- de react with aryl carbamoyl aryl hydrazidoyl chlorides (1 a-f) in ethanol at room temperature to give the corresponding substituted pyrazoles (3 a-f, 6 a-c, 7 a-e and 8 a). The structural as- signments have been made on the basis of elemental analysis, spectral data and the Chemical evidence for the resulting pyrazoles. On the other hand, aminoacetonitriie was reacted with (1 b) and 9 to give the corresponding substituted triazines (13 b) and quinolino 1, 2-f triazine derivative (12). The mechanism of the different reactions were discussed.

References

  • Reaction of aryl carbamoyl aryl hydrazidoyl chlorides with activated nitrile
Year 1990, Volume: 36 , - , 01.01.1990
https://doi.org/10.1501/Commub_0000000450

Abstract

References

  • Reaction of aryl carbamoyl aryl hydrazidoyl chlorides with activated nitrile
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Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

M. K. A. Ibrahım This is me

Publication Date January 1, 1990
Published in Issue Year 1990 Volume: 36

Cite

Vancouver Ibrahım MKA. REACTİON OF ARYL CARBAMOYL ARYL HYDRAZİDOYL CHLO- RIDES WITH ACTIVATED NITRILE. Commun. Fac. Sci. Univ. Ank. Ser. B. 1990;36.

Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

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