Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16471
Title: Synthesis and biological activity of 2-azetidinones, sulphonamides, arylamides and thiourea derivatives
Authors: Patel, Pankaj
Korgaokar, Sushil
Parikh, Khyati
Parekh, Hansa
Issue Date: Jun-1999
Publisher: NISCAIR-CSIR, India
Abstract: 2-Amino-4-[2-(p-chlorobenzenesulphonamido)phenyl]thiazole 1 on condensation with aromatic aldehydes afford 2-benzalamino-4-[2-(p- chlorobenzenesulphonamido)phenyl]thiazole of the type 2. The latter undergoes cyclisation with chloroacetyl chloride in the presence of triethylamine furnishing 2-(4'-aryl-3'-chloro-2'-azetidinon-1'-yl)-4-[2-(p-chlorobenzenesulphonamido) Phenyl]thiazole 3. Thiazole 1 on reaction with different arylsulphonyl chlorides, substituted benzoyl chlorides and various aryl isothiocyanates gives the corresponding 2-aryl sulphonamido-4-[2-(p-chlorobenzene-sulphonamido)phenyl]thiazoles 4, 2-aroylamino-4-[2-(p-chlorobenzenesulphonamido)phenyl]thiazoles 5 and 2- substituted arylthioureidoamino-4-[2-(p-chlorobenzene-sulphonamido)phenyl]thiazoles 6. The products display moderate to good antimicrobial and tuberculostatic activities. The structures of the products 2-6 have been elucidated by elemental analyses and spectral data.
Page(s): 696-700
Appears in Collections:IJC-B Vol.38B(06) [June 1999]

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