2010
DOI: 10.1590/s0103-50532010000600010
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and antimicrobial activity of chromone-linked 2-pyridone fused with 1,2,4-triazoles, 1,2,4-triazines and 1,2,4-triazepines ring systems

Abstract: -diamino-(6-chloro-4-oxo-4H-chromen-3-yl)-2-oxo-1,2-dihydropyridine-3,5-dicarbonitrile (4) with some electrophilic reagents. The structures of the novel compounds were established by elemental analyses and spectral data. All the products were also screened in vitro for their antimicrobial activity. Compounds 7, 9 and 15 showed the highest activities when compared with the reference drugs.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
70
0

Year Published

2012
2012
2022
2022

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 86 publications
(70 citation statements)
references
References 20 publications
(21 reference statements)
0
70
0
Order By: Relevance
“…Chromone and related compounds are wide-spread in nature and exhibit a wide range of pharmacological activity like antibacterial, antifungal (Hatzade et al, 2010, Ali andIbrahim, 2010), antitumor, anti-oxidant, anti-HIV, antiulcerant, anti-inflammatory. As a continuation of our previous work (Nastasă et al, 2013), the present study shows the antimicrobial screening of a new series of 5-(chromene-3-yl)methy-lene-2,4-thiazolidinediones (Figure 1), for which the chemical synthesis and characterization haven't yet been revealed.…”
Section: Sirmentioning
confidence: 99%
“…Chromone and related compounds are wide-spread in nature and exhibit a wide range of pharmacological activity like antibacterial, antifungal (Hatzade et al, 2010, Ali andIbrahim, 2010), antitumor, anti-oxidant, anti-HIV, antiulcerant, anti-inflammatory. As a continuation of our previous work (Nastasă et al, 2013), the present study shows the antimicrobial screening of a new series of 5-(chromene-3-yl)methy-lene-2,4-thiazolidinediones (Figure 1), for which the chemical synthesis and characterization haven't yet been revealed.…”
Section: Sirmentioning
confidence: 99%
“…6‐Chloro‐3‐formylchromone 1 reacts with a primary aromatic amine 39 containing second nucleophilic center to form triazolopyridine derivatives. Cyclocondensation of 39 with 1 in DMF containing piperidine afforded 1,2,3,5‐tetrahydrotriazolo[1,5‐ a ]pyridine derivatives 40 , which was oxidized to 2,7‐ bis (6‐chloro‐4‐oxo‐4 H ‐chromen‐3‐yl)‐5‐oxo‐1,5‐dihdro‐1,2,4‐triazolo[1,5‐ a ]pyridine‐6,8‐dicarbonitrile 41 by ferric chloride in boiling DMSO (Scheme ).…”
Section: Reaction With Nitrogenous Nuclophilesmentioning
confidence: 99%
“…Knoevenagel condensation between 4‐oxo‐4 H ‐1‐benzopyran‐3‐carboxaldehyde 1 and malononitrile in the presence of water gave corresponding condensed product 80 , which further reacted with cyanoacetohydrazide in the presence of a catalytic amount of piperidine gave 39 (Scheme ) .…”
Section: Reaction With Carbon Nucleophilesmentioning
confidence: 99%
“…Condensed pyrido [1,2,4]triazepines are widely reported as important bioactive molecules owing to their versatile biological activities [1][2][3]. Among the significant biological activities of these molecules are the anticancer activities against various cancer cell lines [4,5].…”
Section: Introductionmentioning
confidence: 99%