Journal of Chemical and Pharmaceutical Research (ISSN : 0975-7384)

header
Reach Us reach to JOCPR whatsapp-JOCPR +44 1625708989
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.

Original Articles: 2012 Vol: 4 Issue: 4

Synthesis and antifungal activity of 2-azetidinones, 4-thiazolidinones and 5-imidazolidinones incorporating benzthiazole moiety

Abstract

Starting material 2-amino-5-(benzthiazol-21-yl-thiomethyl)-1, 3, 4-thiadiazole (1) have been synthesized from easily available 2-carboxymethyl thio benzthiazole, thiosemicarbazide and phosphorous oxychloride. Compound (1) reacts with arylaldehyde and methanol gives 2-arylamino-5-(benthiazol-21-yl-thiomethyl)-1, 3, 4-thiadiazole (2 a-g) were reacts with monochloroacetyl chloride and triethyl amine in dioxin to give 2-azetidinones (3 a-g). Compounds (2 a-g) were reacts with mercapto propionic acid / mercapto acetic acid to give 4-thiazolidinones (4 a-n). Compound (1) reacts with 2-phenyl-4-arylidene -5-oxazolone refluxed in pyridine to give 5-imidazolinones (5 a-g). Antifungal activity has been comparied with Dithane M-45, commercial fungicides, for their fungitoxic action against Phytophthora infestans and Collectotricum falcatum and the results correlated with their structural features.