Abstract
Stable primary N-nitrosamines of the benzimidazole series were obtained by the action of sodium amide and isoamyl nitrite on 1-substituted 2-aminobenzimidazoles and subsequent acidification of the resulting benzimidazole-2-diazotates. The effect of the acidity of the solution on the activity of the benzimidazole-2-diazonium salts formed from the nitrosamines was traced.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 689–692, May. 1974.
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Simonov, A.M., Kolodyazhnaya, S.N. & Podladchikova, L.N. Diazo compounds of the heterocyclic series. Chem Heterocycl Compd 10, 596–599 (1974). https://doi.org/10.1007/BF00471337
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DOI: https://doi.org/10.1007/BF00471337