Benzimidazoles by Reaction of Lactones and Thiolactones with o-Phenylene-diamines

Autor:	W. Aten, K. H. Büchel
Rok vydání:	1970
Předmět:	chemistry.chemical_classification chemistry Phenylene General Chemistry Medicinal chemistry Lactone
Zdroj:	Zeitschrift für Naturforschung B. 25:928-931
ISSN:	1865-7117 0932-0776
DOI:	10.1515/znb-1970-0906
Popis:	By refluxing o-phenylene diamines and α-methyl-butyrolactone or γ-thiol-butyrolactone in conc. HCl 2- (γ-hydroxy-propyl) - or 2-(γ-mercapto-propyl) -benzimidazoles are obtained. By further heating or by carrying out the reaction in an excess of the lactone in some cases selfalkylation of the benzimidazoles occurs. The reaction of some more lactones with diamines is described.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9f30a420777571dba3dd4ccf68e92173 https://doi.org/10.1515/znb-1970-0906 Zobrazit plný text záznamu