1983
DOI: 10.1002/jhet.5570200216
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Synthesis of some pyridylamino‐1,4‐disubstituted phthalazines

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.

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Cited by 12 publications
(1 citation statement)
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“…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.…”
Section: Resultsmentioning
confidence: 95%
“…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.…”
Section: Resultsmentioning
confidence: 95%