Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH

<p class="orbitalabstract">Eco-friendly synthesis of some selected Barbiturates, Thiobarbiturates and Dimedone derivatives has been developed by using task specific ionic liquid Bmim[OH], which not only act as catalyst but also  are best solvent media for the Knoevenagel condensation...

Full description

Bibliographic Details
Main Authors: Giribala Madhavrao Bondle, Sandeep T. Atkore
Format: Article
Language:English
Published: Universidade Federal de Mato Grosso do Sul 2019-07-01
Series:Orbital: The Electronic Journal of Chemistry
Subjects:
Online Access:http://orbital.ufms.br/index.php/Chemistry/article/view/1175
id doaj-deec73dbfaa340fc9b5f26b8fdd5333a
record_format Article
spelling doaj-deec73dbfaa340fc9b5f26b8fdd5333a2021-07-07T19:22:40ZengUniversidade Federal de Mato Grosso do SulOrbital: The Electronic Journal of Chemistry1984-64282019-07-0111314215010.17807/orbital.v11i3.1175555Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OHGiribala Madhavrao Bondle0Sandeep T. Atkore1Dept. of Chemistry Dr. BAMUni. Aurangabad IndiaDepartment of Biochemistry, Dr. Babasaheb Ambedkar Marathwada University,Aurangabad- 431004, Maharashtra,India.<p class="orbitalabstract">Eco-friendly synthesis of some selected Barbiturates, Thiobarbiturates and Dimedone derivatives has been developed by using task specific ionic liquid Bmim[OH], which not only act as catalyst but also  are best solvent media for the Knoevenagel condensation reaction between heteroaryl (pyrazole, 2-chloro-quinoline and Indole) aldehydes with barbituric/ thiobarbituric acid and dimedone. High yield and less reaction time are the advantages of this methodology. All the synthesized compounds were tested for their antimicrobial activities. Most of the compounds showed very good antibacterial and antifungal activity.</p><p class="orbitalabstract"> </p><p class="orbitalabstract">DOI: <a href="http://dx.doi.org/10.17807/orbital.v11i3.1175">http://dx.doi.org/10.17807/orbital.v11i3.1175</a></p><p class="orbitalabstract"> </p>http://orbital.ufms.br/index.php/Chemistry/article/view/1175antimicrobial activitybarbituric acid1-butyl-3-methyl-imidazolium hydroxidedimedonequinoline
collection DOAJ
language English
format Article
sources DOAJ
author Giribala Madhavrao Bondle
Sandeep T. Atkore
spellingShingle Giribala Madhavrao Bondle
Sandeep T. Atkore
Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
Orbital: The Electronic Journal of Chemistry
antimicrobial activity
barbituric acid
1-butyl-3-methyl-imidazolium hydroxide
dimedone
quinoline
author_facet Giribala Madhavrao Bondle
Sandeep T. Atkore
author_sort Giribala Madhavrao Bondle
title Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
title_short Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
title_full Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
title_fullStr Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
title_full_unstemmed Synthesis and Biological Evaluation of Some Newly Synthesized Barbiturates and Their Derivatives by Using Task Specific Ionic Liquid [Bmim]OH
title_sort synthesis and biological evaluation of some newly synthesized barbiturates and their derivatives by using task specific ionic liquid [bmim]oh
publisher Universidade Federal de Mato Grosso do Sul
series Orbital: The Electronic Journal of Chemistry
issn 1984-6428
publishDate 2019-07-01
description <p class="orbitalabstract">Eco-friendly synthesis of some selected Barbiturates, Thiobarbiturates and Dimedone derivatives has been developed by using task specific ionic liquid Bmim[OH], which not only act as catalyst but also  are best solvent media for the Knoevenagel condensation reaction between heteroaryl (pyrazole, 2-chloro-quinoline and Indole) aldehydes with barbituric/ thiobarbituric acid and dimedone. High yield and less reaction time are the advantages of this methodology. All the synthesized compounds were tested for their antimicrobial activities. Most of the compounds showed very good antibacterial and antifungal activity.</p><p class="orbitalabstract"> </p><p class="orbitalabstract">DOI: <a href="http://dx.doi.org/10.17807/orbital.v11i3.1175">http://dx.doi.org/10.17807/orbital.v11i3.1175</a></p><p class="orbitalabstract"> </p>
topic antimicrobial activity
barbituric acid
1-butyl-3-methyl-imidazolium hydroxide
dimedone
quinoline
url http://orbital.ufms.br/index.php/Chemistry/article/view/1175
work_keys_str_mv AT giribalamadhavraobondle synthesisandbiologicalevaluationofsomenewlysynthesizedbarbituratesandtheirderivativesbyusingtaskspecificionicliquidbmimoh
AT sandeeptatkore synthesisandbiologicalevaluationofsomenewlysynthesizedbarbituratesandtheirderivativesbyusingtaskspecificionicliquidbmimoh
_version_ 1721314721205846016