Phosphorus, sulfur, and silicon and the related elements · 1994 · 21 citations · 1 references
PharmacyChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryAntibacterial AgentsNovel Antibacterial AgentsPyridazine ChemistryPyrimidine AnalogsPyrimidine AnaloguesPyrimidine Chemistry
Abstract The title compounds (4a-f) were prepared by S-alkylation of 4-cyano-5,6-difur-2′-yl-2H-pyridazine-3-thione (2) and subsequent cyclization in ethanol in the presence of potassium carbonate. Reaction of o-disubstituted thienopyridazines (4a-d) with different reagents afforded tricyclic compounds namely, imidazothienopyridazine (5), pyridazinothienooxazine (6) and pyridazinothienopyrimidines (7–9). Most of the prepared compounds exhibited pronounced antibacterial activity.
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Jpn. Kokai Tokkyo Koho JP 05, 112, 559
H. Shimamure · Medical Entomology and Zoology · 1993 · 481 citations