Issue 14, 1970

1,2,3-Triazole analogues of 2-aminobenzylamine

Abstract

4-Amino-5-aminomethyl-1,2,3-triazoles, further substituted in the 1-, 2-, or 3-position by a methyl- or benzyl-group, were made by reducing the corresponding 4-amino-5-cyanotriazoles, obtained by the reaction of 4-amino-1,2,3-triazole-5-carboxamides with phosphoryl chloride in dimethylformamide [4-dimethylaminomethyleneamino-analogues, e.g.(III), were isolated as intermediates].

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 858-858

1,2,3-Triazole analogues of 2-aminobenzylamine

A. Albert, J. Chem. Soc. D, 1970, 858 DOI: 10.1039/C29700000858

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements