---

Antimicrobial Activity of Synthesised Novel N10-Alkyl Substituted Acridine-9-one Derivatives

Full Text PDF

---

Original Article

Author Details : S. K. Gupta, Pankaj Baboo

Volume : 1, Issue : 1, Year : 2014

Article Page : 39-46

Suggest article by email

Get Permission

Abstract

  

N-Phenyl anthranilic acid was prepared by Ullmann condensation of o-chlorobenzoic acid and aniline. The N-phenyl anthranilic acid was cyclized with polyphosphoric acid over a water bath at 100°C to form acridin-9(10H)-one. N¹⁰-Alkylated acridin-9-ones were synthesized in two series, in first series, N¹⁰-alkylation with 1-bromo-3-chloro propane and in second series with 1, 2-dichloroethane were done by using tetrabutyl ammonium bromide as phase transfer catalyst. Later both were derivatized by refluxing with different secondary amines in presence of potassium carbonate using anhydrous acetonitrile as solvent. The newly synthesized compounds were purified by column chromatography. The formation of title compounds confirmed by physical and spectral data. The synthesized compounds were subjected to microbiological screening. 

 

 

How to cite : Gupta S K, Baboo P, Antimicrobial Activity of Synthesised Novel N10-Alkyl Substituted Acridine-9-one Derivatives. Int J Pharm Chem Anal 2014;1(1):39-46

This is an Open Access (OA) journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.