Synthesis and Some Reactions of 4-Aroyl-3-Chloro-6-p-Tolylpyridazines

Abstract

4-Aroyl-3-chloro-6-p-tolylpyridazines (3a &b) were prepared by the action of phosphorous oxychloride on (2). (3a &b) react with hydrazine hydrate to give the pyrazolinopyridazines (4a &b) and with hydroxylamine hydrochloride to give the isoxazolopyridazines (7a &b), respectively. (4b) was also synthesized by the action of phosphorous oxychloride on the hydrazone (5). The reaction of (3a &b) with primary amines in boiling ethanol gives (8a-e), while their reaction with primary aromatic amines in the presence of solvent gives the Schiff's bases (9a-c).