125179-78-4Relevant articles and documents
FIVE-MEMBERED 2,3-DIOXOHETEROCYCLES. XII. THERMOLYSIS OF 1-ARYL-4-AROYL-5-METHOXYCARBONYL-2,3-DIHYDRO-2,3-PYRROLEDIONES
Maslivets, A. N.,Krasnykh, O. P.,Smirnova, L. I.,Andreichikov, Yu. S.
, p. 941 - 948 (2007/10/02)
The thermolysis of 1-aryl-4-aroyl-5-methoxycarbonyl-2,3-dihydro-2,3-pyrrolediones takes place with the elimination of CO and the formation of the substituted imidoylketene, which undergoes intramolecular cyclization to the 3-aroyl-2-methoxycarbonyl-4-quinolone.The latter reacts with hydrazine to form the 1-aryl-3,4,5,10-tetrahydropyridazinoquinoline-4,10-dione.