Loading…

Macrocycles Containing Nitrogen Heterocycles 11. Calixarene Type Macrocycles Based on m-bis(imidazo[1,5-а]quinoxalin-4(5H)-on-1-yl)benzene for the Encapsulation of Organic Guest Molecules

The interaction of m-bis(3-phenylimidazo[1,5-a]quinoxalin-4(5Н)-on-1-yl)benzene and 3,3'-dibromo-methyl-4-methoxybenzophenone in DMSO or DMF in the presence of t-BuOK or K2CO3, respectively, led to the formation of heterocyclophanes as a result of N,N'-alkylation according to the schemes [...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2014-05, Vol.50 (2), p.237-245
Main Authors: Mamedov, V. A., Gubaidullin, A. T., Khafizova, E. A., Samigullina, A. I., Bauer, I., Habicher, W. D.
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:The interaction of m-bis(3-phenylimidazo[1,5-a]quinoxalin-4(5Н)-on-1-yl)benzene and 3,3'-dibromo-methyl-4-methoxybenzophenone in DMSO or DMF in the presence of t-BuOK or K2CO3, respectively, led to the formation of heterocyclophanes as a result of N,N'-alkylation according to the schemes [1+1] and [2+2] in up to 86% total yield, and the main product from [1+1] N,N'-alkylation was formed in a 57% yield. It was established by X-ray structural analysis that the crystal structure of this product consisted of two independent diastereomeric molecules, and their macroheterocyclic cores were described by an enantiomeric relationship with the accuracy down to the position of the methoxy group in the phenyl fragment.
ISSN:0009-3122
1573-8353
DOI:10.1007/s10593-014-1466-7