Synthesis and comparative anticancer studies of Novel amide functoinalised thienopyridine and pyridothienopyrimidinone derivatives

Amide functionalized trifluoromethyl thieno[2,3-b] pyridine derivatives as a series were prepared starting from reaction between 1,3 di-ketone and thiocyanoacetamide. Compound 3 reacts with bromoethyl acetate to give compound 4. Compound 4 on reaction with diverse substituted aromatic and aliphatic amines gives amide derivatives 5a-f and these amide derivatives on reaction with triethylorthoformate give pyridothienopyrimidinone derivatives 6a-f. All the final compounds were evaluated for anti cancer activity against four human cancer cell lines such as A549—Lung cancer (CCL-185), MCF7—Breast cancer (HTB-22), DU145—Prostate cancer (HTB-81) and HeLa—Cervical cancer (CCL-2) by using MTT assay. Promising compound 5d was identified.

Authors

Publication Details

Journal
Research Journal of Chemistry and Environment
Published
2024-08-30
DOI
https://doi.org/10.25303/2810rjce049054
Citations
1
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.25
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis and comparative anticancer studies of Novel amide functoinalised thienopyridine and pyridothienopyrimidinone derivatives

Naveen Puram, Sailu Betala, Udayasri Bhanothu
1 citations
Research Journal of Chemistry and Environment
Synthesis and biological activity
0.25
article

Synthesis and comparative anticancer studies of Novel amide functoinalised thienopyridine and pyridothienopyrimidinone derivatives

Naveen Puram, Sailu Betala, Udayasri Bhanothu
article en
1 citations

Abstract

Amide functionalized trifluoromethyl thieno[2,3-b] pyridine derivatives as a series were prepared starting from reaction between 1,3 di-ketone and thiocyanoacetamide. Compound 3 reacts with bromoethyl acetate to give compound 4. Compound 4 on reaction with diverse substituted aromatic and aliphatic amines gives amide derivatives 5a-f and these amide derivatives on reaction with triethylorthoformate give pyridothienopyrimidinone derivatives 6a-f. All the final compounds were evaluated for anti cancer activity against four human cancer cell lines such as A549—Lung cancer (CCL-185), MCF7—Breast cancer (HTB-22), DU145—Prostate cancer (HTB-81) and HeLa—Cervical cancer (CCL-2) by using MTT assay. Promising compound 5d was identified.

Research Journal of Chemistry and EnvironmentVol. 28(10)
Openalex Percentile: Top 48%
Synthesis and biological activity
0.25
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.