Synthesis and Antifungal Activity of Azetidinone and Thiazolidinones Derivatives of 2-Amino-6-(2-naphthalenyl)thiazolo[3,2-d]thiadiazole
Author(s) -
K. H. Patel,
A. G. Mehta
Publication year - 2006
Publication title -
journal of chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-9063
pISSN - 2090-9071
DOI - 10.1155/2006/186294
Subject(s) - antifungal , chemistry , combinatorial chemistry , stereochemistry , microbiology and biotechnology , biology
amino-6-(2-naphthalenyl)thiazolo(3,2-d)thiadiazole (1) was prepared by treatment of KCNS and Br 2 on 2-Amino-4-(2-naphthalenyl) thiazole. This amine on facile condensation with aromatic aldehydes afford Schiff Base/anils/azomethines(2a-h). These anils on cyclocondensation reaction with chloro acetyl chloride and thio glycolic acid (i.e. mercapto acetic acid) afford 2- azetidinones and 4-thiazolidinones respectively. The prepared compounds have been screened on some stains of fungai.
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