Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Reaction of N-Aminopyridinium Derivatives. XIII. Syntheses of Pyrazolodiazines by Cyclization of N-Aminodiazinium Salts
KAZUNORI KASUGAMASAAKI HIROBETOSHIHIKO OKAMOTO
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1974 Volume 22 Issue 8 Pages 1814-1826

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Abstract
N-Aminopyridazinium (IV) and N-aminopyrazinium (VI, VIII) derivatives were synthesized by N-amination of pyridazine (III) or pyrazine (V, VII) derivatives with hydroxylamine-O-sulfonic acid. By the reaction of pyrimidine derivatives (IX, XI) with hydroxylamine-O-sulfonic acid, N-aminopyrimidinium derivatives were not obtained, but pyrimidine N-oxide derivatives (X, XII) or 1-amino-4-methyl-6-oxo-1, 6-dihydropyrimidine (XIV, XVI, XVII) were obtained. Therefore, N-aminopyrimidinium derivatives (XXI, XXII, XXIV, and XXVI) were synthesized by N-amination of IX and XI with O-mesitylenesulfonylhydroxylamine. Pyrazolo-diazines (XXVII-XXX, XXXV-XXXVIII) were synthesized by cycloaddition reaction of these N-aminodiazinium derivatives with acetic anhydride and sodium acetate or methyl acetylenecarboxylate. Pyrazolo [1, 5-c] pyrimidine derivatives (XXXVII-XXXVIII), which are different in oriention, were obtained by 1, 3-dipolar cycloaddition reaction of XXI and XXIV with methyl acetylenecarboxylate.
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© The Pharmaceutical Society of Japan
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