Synthesis and Cytotoxic Studies of Quinazoline-Triazole Hybrid Aza Heterocycles

dc.contributor.author Vodnala, Sumathi
dc.contributor.author Bhavani, Anagani Kanaka Durga
dc.contributor.author Pagilla, Shankaraiah
dc.contributor.author Allam, Muralidhar
dc.contributor.author Rayala, Nagamani
dc.contributor.author Mudiraj, Anwita
dc.contributor.author Babu, Phanithi Prakash
dc.date.accessioned 2022-03-27T05:16:20Z
dc.date.available 2022-03-27T05:16:20Z
dc.date.issued 2021-11-01
dc.description.abstract Abstract: Herein, we report a series of 1,2,3-triazole combined with quinazoline hybrid heterocyclic compounds by 1,3-dipolar cycloaddition reaction catalyzed by Cu(I). This reaction has been carried out between quinazoline based alkyne and aryl/benzyl azides under optimized conditions. Modification of 4-hydroxyquinazoline by propargyl bromide in presence of potassium carbonate gives a corresponding alkyne. Structure of the synthesized compounds has been characterized by IR, 1H, and 13C NMR, ESI-Mass, and HRMS spectra. The products have been tested for anticancer activity against C6 glioma cell lines and characterized by moderate cytotoxic activity.
dc.identifier.citation Russian Journal of General Chemistry. v.91(11)
dc.identifier.issn 10703632
dc.identifier.uri 10.1134/S1070363221110189
dc.identifier.uri https://link.springer.com/10.1134/S1070363221110189
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/7611
dc.subject 1,2,3-triazoles
dc.subject 1,3-dipolar cycloaddition
dc.subject azides
dc.subject cytotoxicity
dc.subject quinazoline
dc.title Synthesis and Cytotoxic Studies of Quinazoline-Triazole Hybrid Aza Heterocycles
dc.type Journal. Article
dspace.entity.type
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: