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New [<i>g</i>]‐fused [1,2,4]triazolo[1,5‐<i>c</i>]pyrimidines: Synthesis of pyrido[3,2‐<i>e</i>] and [4,3‐<i>e</i>][1,2,4]triazolo[1,5‐<i>c</i>]pyrimidine, pyrimido[5,4‐<i>e</i>][1,2,4]triazolo[1,5‐<i>c</i>]pyrimidine and [1,2,4]triazolo[1,5‐<i>c</i>]pteridine derivatives
18
Citations
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References
1994
Year
DerivativesHeterocyclicMedicineDifferent PathwaysOrganic ChemistrySynthetic ChemistryDerivatives 7,8AChemistryHeterocycle ChemistryPharmacologyPharmaceutical ChemistryNew Tricyclic HeterocyclesDrug Discovery
Abstract A number of 2‐aryl‐substituted pyrido[3,2‐ e ] and [4,3‐ e ][1,2,4]triazolo[1,5‐ c ]pyrimidines and [1,2,4]triazolo[1,5‐ c ]pteridines 11,12a,b,e , their corresponding 5‐carbonyl derivatives 7,8a,b,e and some pyrimido[5,4‐ e ][1,2,4]triazolo[1,5‐ c ]pyrimidin‐5‐ones 7,8c,d have been synthesized, according to different pathways. The new tricyclic heterocycles were prepared with the aim of studying their possible benzodiazepine receptors affinity.
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