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Heteroelectrocyclic reaction of 4‐azido‐3‐hydrazonoalkyl‐quinolines to 2‐arylaminopyrazolo[4,3‐<i>c</i>]quinolones
19
Citations
12
References
2000
Year
DerivativesHeterocyclicAzides 4Heteroelectrocyclic ReactionOrganic ChemistryThermal Decomposition ConditionsAbstract 4‐Azido‐3‐acylquinolonesChemistryHeterocycle ChemistryPharmacologySynthetic Chemistry
Abstract 4‐Azido‐3‐acylquinolones 4 obtained from 4‐hydroxy derivatives 1 via tosylates 3 or chlorides 5, reacted with arylhydrazines 6 to generate 4‐azido‐3‐hydrazonoalkylquinolines 7. Thermolysis of 7 gave ring closure products which were assigned to 2‐arylaminopyrazolo[4,3‐ c ]quinolones 10. The thermal decomposition conditions of the azides 4 and 7 were studied by differential scanning calorimetry (DSC).
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