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Stadlbauer W., Hojas G., Fiala W.,
Proceedings of the Second International Electronic Conference on
Synthetic Organic Chemistry (ECSOC-2),
S.-K. Lin, E. Pombo-Villar (Eds), MPDI, Basel, 1999;
CD-ROM edition, ISBN 3-906980-01-4, A0001
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Abstract: 1-Azido-2-hydrazonoacyl-3-oxo-heterocycles , which were obtained from the corresponding acyl derivatives ,
cyclize upon thermolysis to give 2-arylamino-pyrazolo[4,3-c]fused compounds.
The cyclization conditione were studied by differential scanning calorimetry (DSC). Structure elucidation by 13C nmr excluded
the formation of triazino isomers.
Attempts to use a reversed reaction path by azidation of the tosylates
resulted always in the cyclization to the 1-aryl-pyrazolo[4,3-c]fused compounds.
Theses pyrazols could be obtained also from other precursors, the corresponding hydroxy-hydrazonoacyl compounds by thermal decomposition.
1-Aryl-pyrazolo[4,3-c]quinolin-2-ones are of interest because of their
potential biological activity
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