Abstract:Two general procedures involving the condensation of phthalonitrile or 1,3‐diiminoisoindoline with various aminopicolines, followed by ring expansion with hydrazine to the corresponding phthalazine are described. Syntheses are reported of 1, 4‐di(3′‐methyl‐2′‐pyridyl) aminophthalazine, 1,4‐di(5′‐methyl‐2′‐pyridyl)aminophthalazine, and 1,4‐di(4′, 6′‐dimethyl‐2′‐pyridyl)aminophthalazine.
“…Clearly the tautomeric mixture involves NH protons at both ring and exocyclic sites, a feature observed for the related ligand l,4-bis(2'pyridylaminojphthalazine and its alkylated derivatives. 13 In these compounds, NH resonances were observed at 8.7-8. "B^i s the mean of the principal axes of the thermal ellipsoid.…”
“…Clearly the tautomeric mixture involves NH protons at both ring and exocyclic sites, a feature observed for the related ligand l,4-bis(2'pyridylaminojphthalazine and its alkylated derivatives. 13 In these compounds, NH resonances were observed at 8.7-8. "B^i s the mean of the principal axes of the thermal ellipsoid.…”
2‐Amino‐pyridine (II) reagieren mit Phthalsäuredinitril (I) beim Erhitzen über die Diimino‐isoindoline (III) und anschließendem Behandeln mit Hydrazin zu den Pyridylamino‐phthalazinen (IV), die auch aus Diimino‐isoindolin (V) erhalten werden können.
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