Cyclocondensation of 5-chloro-4-formylpyrrole-3-carboxylates with arylamines. Synthesis and fluorescent properties of pyrrolo[2,3-b]quinoline-3-carboxylates and their benzo[f] analogs

Autor:	Eduard B. Rusanov, M. V. Vovk, Vladislav M. Polishchuk, A. N. Grozav, Nikolay P. Shandura, Mariana Z. Fedoriv, Vitaliy А. Chornous, Sergiy V. Kemskiy
Rok vydání:	2021
Předmět:	chemistry.chemical_compound chemistry Organic Chemistry Quinoline Alkaline hydrolysis (body disposal) Medicinal chemistry Fluorescence
Zdroj:	Chemistry of Heterocyclic Compounds. 57:1024-1030
ISSN:	1573-8353 0009-3122
Popis:	5-Chloro-4-formylpyrrole-3-carboxylates react with anilines or β-naphthylamine when heated in DMF under reflux to form ethyl pyrrolo[2,3-b]quinoline-3-carboxylates or their benzo[f] analogs, which exhibit moderate fluorescent properties. The corresponding carboxylic acids were obtained by alkaline hydrolysis of the synthesized carboxylates.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::1782cc4edd425858e7840ed485ec57ec https://doi.org/10.1007/s10593-021-03017-y Zobrazit plný text záznamu Plný text ve formátu PDF