Abstract
Procedures for high-yield syntheses of 2-ethoxy- and 2-dimethylamino-4-arylpyrido [2,3-d]pyridazines (3a, b, 5), 3-alkyl- and 1-alkyl-4-aryl-1,2-dihydro-2-oxopyrido[2,3-d]pyridazines (4b, 6) as well as ethyl 4-aryl-1,2-dihydro-2-oxopyrido[2,3-d]pyridazine-3-carboxylates (7a, b) starting from 5-amino-4-pyridazinyl aryl ketones (1a, b) are reported. Considerable variability of the substitution pattern in the pyridine moiety of this bicyclic system is provided by the proposed strategy of annelation of the pyridine ring to a preformed pyridazine nucleus.

This publication has 0 references indexed in Scilit: