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A novel crystalline tetrazolo‐azido isomer pair: Pyrido[ 2,3‐<i>e</i>] tetrazolo[5,1‐<i>c</i>]‐<i>as</i>‐triazine and 3‐azidopyrido[2,3‐<i>e</i>]‐<i>as</i>‐triazine; the synthesis of tetrazolo[5,1‐<i>c</i>] benzo‐<i>as</i>‐triazine and pyrido[2,3‐<i>e</i>]‐<i>s</i>‐triazolo[3,4‐<i>c</i>] ‐<i>as</i>‐triazine
27
Citations
5
References
1973
Year
Chemical EngineeringEngineeringHeterocyclic‐Triazine 1‐OxideOrganic ChemistryNew Ring SystemChemistryHeterocycle ChemistryPharmacologySynthetic ChemistryInorganic SynthesisCrystalline Form
Abstract The deoxygenated derivative of 3‐azidobenzo‐ as ‐triazine 1‐oxide (II) exists in solution predominantly as 3‐azidobenzo‐ as ‐triazine form (IVa) but in the crystalline state as tetrazolo[5,]‐ c ]‐benzo‐ as ‐triazine (IVb), a new fused heteroaromatie ring system. With the pyrido[2,3‐ e ]‐ as ‐triazine derivatives, however, both 3‐azidopyrido[2,3‐ e ]‐ as ‐triazine (X) and pyrido[2,3‐ e ] tetra‐zolo[5,1‐ e ]‐ as ‐triazine (XI) can be isolated in crystalline form, and these are interconvertible. Another new ring system, the pyrido[2,3‐ e ] triazolo [3,4‐ c ]‐ as ‐triazine (XVII) and its derivatives has also been synthesized.
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