Issue 8, 1978

Triazines and related products. Part 21. Cyclisation of 3-amino-5-hydrazinopyrazole and 3-amino-5-hydrazino-1,2,4-triazole to azolo[5,1-c][1,2,4]triazines

Abstract

Interaction of malononitrile with two equivalents of hydrazine hydrate affords 3-amino-5-hydrazinopyrazole in high yield. The pyrazole reacts with ethyl pyruvate, diacetyl, and benzil to yield derivatives of 2-aminopyrazolo[5,1-c][1,2,4]triazine: amino-1,2,4-triazolo[5,1-c][1,2,4]triazines are similarly formed from 3-amino-5-hydrazino-1,2,4-triazole.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1978, 885-888

Triazines and related products. Part 21. Cyclisation of 3-amino-5-hydrazinopyrazole and 3-amino-5-hydrazino-1,2,4-triazole to azolo[5,1-c][1,2,4]triazines

E. J. Gray, H. N. E. Stevens and M. F. G. Stevens, J. Chem. Soc., Perkin Trans. 1, 1978, 885 DOI: 10.1039/P19780000885

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