AN EFFICIENT IMPROVED SYNTHESIS OF NPHENYLCINNAMAMIDE ANALOGOUS PROMOTED BY CDI / ET3N.
D. Ramakrishna, B. Priyanka and Dr. N. Krishna Rao*
Abstract
The synthetic pathways protocol followed by antimicrobial study of Nphenylcinnamamide
(4).These derivatives can be synthesized from
cinnamoylchloride (2) with substituted aromatic anilines (3)in the
presence of dehydro halogenating reagent such as triethyl amine and
CDI in methylene dichloride at reflux. The compound (2) also can be
prepared from cinnamic acid and thionylchloride in the presence of
MDC at 5-100C. All the derivatives evaluated by advanced spectral
data (1HNMR, 13CNMR & LCMS) and the structure of the all titled
compounds can be determined by elemental analysis. In addition to
evaluation of ant-microbial activities against four bacterial strains as
well as two fungal strains.
Keywords: Cinnamoylglycine substituted aromatic amines, CDI, N-phenylcinnamamide. Antimicrobial activity.
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