Synthesis and antimicrobial activity of new 4-thiazolidinone derivatives containing 2-amino-6-methoxybenzothiazole

A novel series of Schiff bases 5a– j and 4-thiazolidinones 6a– j have been prepared from the building blocks 2-chloro pyridine-3-carboxylic acid [ 1] and 2-amino-6-methoxy-benzothiazole [ 2]. All of the synthesized compounds have been confirmed by elemental analyses, IR, 1H NMR and 13C NMR spectral...

Full description

Saved in:
Bibliographic Details
Published in:Saudi pharmaceutical journal Vol. 18; no. 3; pp. 129 - 136
Main Authors: Patel, Navin B., Shaikh, Faiyazalam M.
Format: Journal Article
Language:English
Published: Saudi Arabia Elsevier B.V 01-07-2010
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:A novel series of Schiff bases 5a– j and 4-thiazolidinones 6a– j have been prepared from the building blocks 2-chloro pyridine-3-carboxylic acid [ 1] and 2-amino-6-methoxy-benzothiazole [ 2]. All of the synthesized compounds have been confirmed by elemental analyses, IR, 1H NMR and 13C NMR spectral data. These newly synthesized compounds were screened for their antimicrobial activity. Variable and modest activity was observed against the investigated strains of bacteria and fungi, however, compound 6h revealed significant antibacterial activity against Escherichia coli. Compounds 1, 2, 3, 5c, 5g and 5h, on the other hand, revealed potent antifungal activity against Candida albicans compared to the reference drug greseofulvin.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1319-0164
2213-7475
DOI:10.1016/j.jsps.2010.05.002