Chemistry of the Heterocyclic Pseudobasic Amino Alcohols, XXXVIII Ring‐Chain Tautomerism of Pyrimido[6,1‐a]isoquinolines

Dezsö Korbonits, GÁBor Horváth, KÁLmÁN Simon, P. Kolonits

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Abstract

In basis media, 4‐substituted pyrimido[6,1‐a]isoquinolin‐2‐imine hydrochlorides (4) constitute an equilibrium system involving the tautomeric forms characteristic of pseudobases 5, 6, 7 and the anhydro base 9. In aqueous solution in the pH range 7–13 the ammonium hydroxide form 5 is present. Between pH 13 and 14 the pseudobase 6 probably arises from this by covalent binding of the hydroxy group. 6 is then converted to the more stable imino type anhydrobase 9. Ring cleavage of 4 by excess alkali or of 9 by a small amount of water gives 1‐(acylamidinomethylen)isoquinolines 7. Compounds 7 and 9 are stable in the solid state or in aprotic solutions but revert to cation 5 in dilute protic solutions.

Original languageEnglish
Pages (from-to)493-498
Number of pages6
JournalChemische Berichte
Volume123
Issue number3
DOIs
Publication statusPublished - 1990

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Keywords

  • Pyrimido[6,1‐a]isoquinolines / Pseudobases, heterocyclic / Ring‐chain tautomerism

ASJC Scopus subject areas

  • Chemistry(all)

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