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Piperidine mediated synthesis of n-heterocyclic chalcones and their antibacterial activity

✍ Scribed by P. Venkatesan; S. Sumathi


Publisher
Journal of Heterocyclic Chemistry
Year
2009
Tongue
English
Weight
80 KB
Volume
47
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

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The chalcones 1‐(2′‐hydroxy‐aryl)‐3‐(1‐indol‐3‐yl)‐prop‐2‐en‐1‐one (3) and 1‐(2′‐hydroxy‐aryl)‐3‐(2‐chloroquinolin‐3‐yl)‐prop‐2‐en‐1‐one (6) were synthesised by piperidine mediated condensation of an ethanolic solution of an o‐hydroxyacetophenone (1) with corresponding heteroaryl‐3‐carboxaldehyde. The structures have been established on the basis of elemental (C, H, N) analysis, UV, IR, ^1^H NMR spectral data. The compounds 3 and 6 were screened for antimicrobial activities against a variety of bacterial agents. J. Heterocyclic Chem., 2010.


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Piperidine-mediated synthesis of thiazol
✍ P. Venkatesan; T. Maruthavanan 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 107 KB

## Abstract A series of new thiazolyl chalcones, 1‐[2‐amino‐4‐methyl‐1, 3‐thiazol‐5‐yl]‐3‐aryl‐prop‐2‐en‐1‐one were prepared by piperidine mediated Claisen‐Schmidt condensation of thiazolyl ketone with substituted aromatic aldehyde. These chalcones on cyclization gave 2‐amino‐6‐(2‐amino‐4‐methyl‐1,