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...
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Published in: | Saudi pharmaceutical journal Vol. 18; no. 3; pp. 129 - 136 |
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Main Authors: | , |
Format: | Journal Article |
Language: | English |
Published: |
Saudi Arabia
Elsevier B.V
01-07-2010
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Subjects: | |
Online Access: | Get full text |
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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. |
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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 |