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A novel crystalline tetrazolo‐azido isomer pair: Pyrido[ 2,3‐ e ] tetrazolo[5,1‐ c ]‐ as ‐triazine and 3‐azidopyrido[2,3‐ e ]‐ as ‐triazine; the synthesis of tetrazolo[5,1‐ c ] benzo‐ as ‐triazine and pyrido[2,3‐ e ]‐ s ‐triazolo[3,4‐ c ] ‐ as ‐triazine
Author(s) -
Messmer A.,
Hajós Cy.,
Benkó P.,
Pallas L.
Publication year - 1973
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570100426
Subject(s) - chemistry , triazine , ring (chemistry) , derivative (finance) , stereochemistry , medicinal chemistry , organic chemistry , economics , financial economics
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.