Synthesis of quinolyl-substituted 4,7-phenanthrolines

Autor:	K. N. Gusak, N. S. Kozlov, V. A. Serzhanina
Rok vydání:	1990
Předmět:	chemistry.chemical_compound Chemistry medicine.drug_class Organic Chemistry Mass spectrum medicine Hydrochloric acid Ring (chemistry) Medicinal chemistry Aminoketone
Zdroj:	Chemistry of Heterocyclic Compounds. 26:664-668
ISSN:	1573-8353 0009-3122
Popis:	1-(2-Quinolyl)-3-aryl-4,7-phenanthrolines were synthesized by reacting arylidene-6-quinolylamines with 2-acetylqidnoline in n-butanol in the presence of hydrochloric acid. It was found that the formation of the 4,7-phenanthroline ring is preceded by the stage of formation of an intermediate aminoketone, 1-(2-quinolyl)-3-phenyl-3-(6-quinolylamino)propan-1-one. The IR, UV, PMR, and mass spectra of the synthesized compounds are discussed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::245da449d1c0d386557d406b14486c73 https://doi.org/10.1007/bf00756419 Zobrazit plný text záznamu Full text from SpringerLink