Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Heterocyclic imines and amines. Part XIII. 3,6-Dihydrazinopyridazine and the nature of the reaction between 3,6-dimethoxypyridazine and hydrazine

Elvidge, J. A. and Pickett, J. A. ORCID: https://orcid.org/0000-0002-8386-3770 1972. Heterocyclic imines and amines. Part XIII. 3,6-Dihydrazinopyridazine and the nature of the reaction between 3,6-dimethoxypyridazine and hydrazine. Journal of the Chemical Society, Perkin Transactions 1 , pp. 1483-1488. 10.1039/p19720001483

Full text not available from this repository.

Abstract

A route to 3,6-dihydrazinopyridazine from dithiomaleohydrazide is confirmed and improved and the product now characterised. Possible alternative routes,e.g, from 3,6-dichloro-, -diphenoxy-, and -dimethylthio-pyridazine, yielded the monohydrazino-compounds, whilst 3,6-di-p-tolylsulphonyloxypyridazine with hydrazine afforded maleodihydrazide. A previously described method from 3,6-dimethoxypyridazine and hydrazine is shown to yield a mixture of oxygen-containing products, deduced as comprising 6-hydrazino-5-amino-2,3-dihydro-3-oxopyrid-azine together with some of the 6-methoxy-analogue.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Schools > Chemistry
ISSN: 1364-5463
Last Modified: 26 Jan 2026 10:57
URI: https://orca.cardiff.ac.uk/id/eprint/184117

Actions (repository staff only)

Edit Item Edit Item