66751-91-5Relevant academic research and scientific papers
Five-Membered 2,3-Dioxo Heterocycles. XXXIX. Reaction of 4-Aroyl-1-aryl-5-methoxycarbonyl- and 1-Aryl-4-isopropyloxalo-5-phenyl-2,3-dihydropyrrole-2,3-diones with o-Phenylenediamine
Maslivets, A. N.,Smirnova, L. I.,Ivanenko, O. I.,Andreichikov, Yu. S.
, p. 563 - 568 (2007/10/03)
4-Aroyl-1-aryl-5-methoxycarbonyl- and 1-aryl-4-isopropyloxalo-5-phenyl-2,3-dihydropyrrole-2,3-diones react with p-phenylenediamine to give substituted 1,2,3,5,10,10a-hexahydropyrrolobenzodiazepine-2,3-diones.Hydrolysis of the latter yields 3-phenacylidene-1,2,3,4-tetrahydroquinoxalin-2-ones.
CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXXV. KINETICS OF THE FORMATION OF 3-PHENACYLIDENE-3,4-DIHYDRO-2-QUINOXALONES FROM ARYLAMIDES OF AROYLPYRUVIC ACIDS AND o-PHENYLENEDIAMINE
Andreichikov, Yu.S.,Kozlov, A.P.,Kurdina, L.N.
, p. 752 - 756 (2007/10/02)
The kinetics of the acid-catalyzed reactions of the arylamides of aroylpyruvic acids with o-phenylenediamine, leading to the formation of 3-phenacylidene-2-quinoxalones, were investigated.It was established that the reaction rate is controlled by nucleophilic attack by the amide carbonyl at the cyclization stage.
