PYRIDAZINE DERIVATIVES AND RELATED-COMPOUNDS .4. PYRROLO{[}2,3-C]PYRIDAZINES AND FURO{[}2,3-C]PYRIDAZINES, SYNTHESIS AND SOME REACTIONS

Ethyl 5-amino-3,4-diphenyl-7 H-pyrrolo{[}2,3-c]pyridazine-6-carboxylate (1), ethyl 5-amino-furo{[}2,3-c]pyridazine-6-carboxylate (2) and 5-aminofuro{[}2,3-c]pyridazine-6-carboxamide (3), are obtained from 4-cyano-5,6-diphenyl-3(2H)-pyridazinone. 5-Acetamido and 5-chloroacetamido derivatives prepared from 1, undergo cyclization on heating to form 2-substituted pyridazino{[}4',3':4,5]pyrrolo{[}3,2-d]oxazin-4(5 H)-one (5a, b). The The reaction of 1 and 2 with hydrazine gave 6-carbohydrazide derivatives (7a, b). Compound 3 undergoes condensation with acetyl chloride, chloroacetyl chloride, benzoyl chloride, formamide and carbon disulphide to furnish the corresponding pyrimido{[}4',5':4,5]furo{[}2,3-c]pyridazin-4(3 H)-one derivatives. The reaction of 1 with o-aminophenol gave 3,4-diphenyl-1 1-oxo-10, 11-dihydro-12 H-pyridazino{[}4',3':4,5]pyrrolo{[}3,2-b]{[}1,5]benzoxazepine.