𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and in vitro antimicrobial activity of new 3-(2-morpholinoquinolin-3-yl) substituted acrylonitrile and propanenitrile derivatives

✍ Scribed by Jigar A. Makawana; Manish P. Patel; Ranjan G. Patel


Book ID
111491486
Publisher
Versita
Year
2011
Tongue
English
Weight
194 KB
Volume
65
Category
Article
ISSN
0366-6352

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A series of new 3-(2-morpholinoquinolin-3-yl)acrylonitrile derivatives (IVa-IVf) has been synthesised by the base-catalysed condensation reaction of 2-morpholinoqionoline-3-carboxaldehydes (IIa-IIc) and 2-cyanomethylbenzimidazoles (IIIa-IIIb). Subsequent regiospecific reduction of the C—C double bond in acrylonitrile moiety afforded 3-(2-morpholinoquinolin-3-yl)propanenitrile derivatives (Va-Vf). All the compounds synthesised were subjected to in vitro antimicrobial screening against some representatives of bacteria and fungi. The majority of the compounds were found to be active against Gram-positive bacteria Bacillus subtilis and Clostridium tetani as well as against the fungal pathogen Candida albicans.


📜 SIMILAR VOLUMES


Convenient Synthesis and Antimicrobial A
✍ Bakr F. Abdel-Wahab; Hatem A. Abdel-Aziz; Essam M. Ahmed 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 474 KB 👁 2 views

## Abstract The reaction of ethyl 4‐(benzofuran‐2‐yl)‐2,4‐dioxobutanoate **2** with two moles of hydrazine hydrate afforded 5‐(benzofuran‐2‐yl)‐1__H__‐pyrazole‐3‐carbohydrazide **4a**, while its reaction with equimolar amount of phenylhydrazine gave ester **3b** which then converted to 5‐(benzofura

Synthesis and antimicrobial activity of
✍ Adel A.-H. Abdel-Rahman; Wael A. El-Sayed; El-Sayed G. Zaki; Asem A. Mohamed; Ah 📂 Article 📅 2011 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 160 KB

## Abstract A number of new [(pyrazol‐4‐yl)methylene]hydrazono‐2,3‐dihydrothiazole derivatives, their sugar hydrazones and __N__‐glycosides were synthesized. Furthermore, __N__‐substituted oxygenated alkyl and hydroxyl derivatives and 1,3,4,‐oxadiazoline acyclic nucleoside analogs were prepared. Th