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July 1, 1987Journal of Heterocyclic Chemistry

“One pot” synthesis of 2,9‐disubstituted 8‐azaadenines (3,5‐disubstituted 7‐amino‐3H‐1,2,3‐triazolo[4,5‐d]pyrimidines)

P. L. BARILI Giuliana Biagi Oreste Livi Luciana Mucci Valerio Scartoni

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Abstract

A new simple method for the synthesis of title compounds is described starting from malononitrile, benzyl‐azide and an aliphatic or aromatic nitrile.

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BARILI et al. (1987) studied this question.

synapsesocial.com/papers/6a92298aa10c1849f25eeeac https://doi.org/10.1002/jhet.5570240419

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1A facile “one pot” synthesis of 2,9‐disubstituted 8‐azapurin‐6‐ones (3,5‐disubstituted 7‐hydroxy‐3H‐1,2,3‐triazolo[4,5‐d]pyrimidines)Original Research · 1985 · 22 citations
2The metabolism of 8-azapurinesOriginal Research · 1957 · 78 citations
3Structure of coformycin, an unusual nucleoside of microbial originOriginal Research · 1974 · 125 citations
4Synthesis and biological evaluation of 2-fluoro-8-azaadenosine and related compoundsOriginal Research · 1983 · 32 citations
5Antiallergic activity of 2-phenyl-8-azapurin-6-onesOriginal Research · 1975 · 54 citations

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