ChemInform Abstract: Synthesis of Quinolyl-Substituted 4,7-Phenanthrolines

Autor:	K. N. Gusak, V. A. Serzhanina, N. S. Kozlov
Rok vydání:	2010
Předmět:	chemistry.chemical_compound chemistry medicine.drug_class Polymer chemistry medicine Mass spectrum Organic chemistry Hydrochloric acid General Medicine Ring (chemistry) Aminoketone
Zdroj:	ChemInform. 22
ISSN:	0931-7597
DOI:	10.1002/chin.199112233
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_________::3109975cd74b764e93c6d60acdc35771 https://doi.org/10.1002/chin.199112233 Zobrazit plný text záznamu Plný text