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Aminomethylation of 1,2,4-triazoles and tetrazoles

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Aminomethylation was accomplished in a series in which the starting amino compounds and the components of acidic character belong to the azole class. Two-ring Mannich bases are formed in the reaction of 4-amino-1,2,4-triazole or N-methyl-5-aminotetrazole in an aqueous medium with formaldehyde and NH-triazoles, the acidic properties of which are known.

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Literature cited

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 549–551, April, 1982.

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Ostapkovich, A.M., Shevtsov, V.P. Aminomethylation of 1,2,4-triazoles and tetrazoles. Chem Heterocycl Compd 18, 423–425 (1982). https://doi.org/10.1007/BF00503568

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  • DOI: https://doi.org/10.1007/BF00503568

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