Department of Pharmaceutical Chemistry, PES College of Pharmacy, Bangalore-50, Karnataka, India
*Corresponding Author E-mail: roopad24@gmail.com
Online published on 19 June, 2014.
2-amino-3-N-(substituted carboxanilido)-4, 5-disubstituted thiophenes 1a – 1h were synthesized using versatile Gewald reaction. First step is preparation of substituted cyanoacetanilides (Comp. No JSR a and b) which was carried out by Substituted anilines and Ethyl cyano acetate which was then reacted with Methylenic ketone, ammonium acetate, glacial acetic acid, benzene, sulphur to produce 2-amino-3-N-(substituted carboxanilido)-4, 5-disubstituted thiophenes JSR 1a–1h. Later the compound was subjected to diazotization to yield eight new thieno triazines. The compounds were characterized IR, 1H NMR and mass spectral data and screened for anti-fungal activity.
Synthesis, Thiophenes, Thienotriazines, Spectral analysis, Antifungal activity