Синтез та діуретичні властивості n-арил-6-гідрокси-2-метил-4-оксо-2,4-дигідро-1н-піроло[3,2,1-ij] хінолін-5-карбоксамідів з електроно-акцепторними замісниками в анілідному фрагменті

• Дата: 2013
• Автори: Ukrainets, I. V., Golik, M. Yu., Shemchuk, O. L., Kravchenko, V. M.
• Формат: Стаття
• Мова: English
• Опубліковано: National University of Pharmacy 2013
• Теми: аніліди; 4-гідрокси-2-оксо-1; 2-дигідрохінолін-3-карбоксаміди; піролохіноліни; амідування; гідроліз; діуретична активність; УДК 547.298.1; 547.831.9; 615.254.1; 615.276
• Онлайн доступ: https://ophcj.nuph.edu.ua/article/view/ophcj.13.741
• Назва журналу: Journal of Organic and Pharmaceutical Chemistry

In numerous studies of 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxamides it has been convincingly shown that amidation of quinoline-3-carboxylic acids esters with alkyl-, aryl- and hetarylamines is the best way to obtain these compounds. As a rule, syntheses proceed smoothly and efficiently under rather mild conditions. However, in those cases when for formation of amides the temperature of 120-150°C and above is applied, partial destruction of the ester fragment may occur and, as a result, it pollutes the target products with specific impurities – the corresponding 4-hydroxy-1,2- dihydroquinolin-2-ones or their analogues. Application of 1H NMR spectroscopy allows to prove that the cause of ester fragments destruction, which sometimes can be observed when alkyl 4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylates react with amines under harsh conditions, is water presented in the reagents or in the solvents. It becomes clear from this study that at the temperature of 95°C and higher the sensitivity of 4-hydroxy-2-oxo-1,2-dihydroquinoline- 3-carboxylic acids esters in a solution or a melt to hydrolysis increases significantly. Simple methods to minimize this undesirable process have been proposed – if the synthesis of N-substituted amides based on them requires such severe conditions, water should be removed from the reagents and solvents in order to avoid contamination of the final products with 4-hydroxy-1,2-dihydroquinolin-2-ones. The results of the diuretic properties study of new substituted anilides of 6-hydroxy-2-methyl-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid are discussed.