Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities

A total of 12 bis(acylthiourea) derivatives with different pharmacophores have been synthesized via nucleophilic substitution reaction of benzene-1,4-dicarbonyl isothiocyanate intermediate with aromatic amine bearing halogens at the ortho, meta and para positions. The structures of the synthesised c...

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Main Authors: Ainaa Nadiah, Abd Halim, Zainab, Ngaini
Format: Article
Published: Taylor & Francis 2017
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Online Access:http://ir.unimas.my/id/eprint/18505/
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author Ainaa Nadiah, Abd Halim
Zainab, Ngaini
author_facet Ainaa Nadiah, Abd Halim
Zainab, Ngaini
author_sort Ainaa Nadiah, Abd Halim
building UNIMAS Institutional Repository
collection Online Access
description A total of 12 bis(acylthiourea) derivatives with different pharmacophores have been synthesized via nucleophilic substitution reaction of benzene-1,4-dicarbonyl isothiocyanate intermediate with aromatic amine bearing halogens at the ortho, meta and para positions. The structures of the synthesised compounds were confirmed by CHN elemental analysis, FT-IR, ¹H NMR and ¹³C NMR spectroscopies. Antibacterial studies of the compounds via the Kirby Bauer disc diffusion method against Escherichia coli (E.coli) ATCC 25922 and Staphylococcus aureus (S. aureus) S48/81 demonstrated that bis(acylthiourea) N¹,N⁴-bis[(2-chlorophenyl)carbamothioyl]terephthalamide (4) and N¹,N⁴-bis[(2-bromophenyl)carbamothioyl]terephthalamide (7) bearing Cl and Br at the ortho position exhibited excellent activities against both bacteria strains compared to ampicillin standard.
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spelling unimas-185052017-11-09T07:36:16Z http://ir.unimas.my/id/eprint/18505/ Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities Ainaa Nadiah, Abd Halim Zainab, Ngaini Q Science (General) A total of 12 bis(acylthiourea) derivatives with different pharmacophores have been synthesized via nucleophilic substitution reaction of benzene-1,4-dicarbonyl isothiocyanate intermediate with aromatic amine bearing halogens at the ortho, meta and para positions. The structures of the synthesised compounds were confirmed by CHN elemental analysis, FT-IR, ¹H NMR and ¹³C NMR spectroscopies. Antibacterial studies of the compounds via the Kirby Bauer disc diffusion method against Escherichia coli (E.coli) ATCC 25922 and Staphylococcus aureus (S. aureus) S48/81 demonstrated that bis(acylthiourea) N¹,N⁴-bis[(2-chlorophenyl)carbamothioyl]terephthalamide (4) and N¹,N⁴-bis[(2-bromophenyl)carbamothioyl]terephthalamide (7) bearing Cl and Br at the ortho position exhibited excellent activities against both bacteria strains compared to ampicillin standard. Taylor & Francis 2017 Article PeerReviewed Ainaa Nadiah, Abd Halim and Zainab, Ngaini (2017) Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities. Phosphorus, Sulfur, and Silicon and the Related Elements, 192 (9). ISSN 10426507 https://www.researchgate.net/publication/316030203 DOI: 10.1080/10426507.2017.1315421
spellingShingle Q Science (General)
Ainaa Nadiah, Abd Halim
Zainab, Ngaini
Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title_full Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title_fullStr Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title_full_unstemmed Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title_short Synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
title_sort synthesis and characterisation of halogenated bis(acylthiourea) derivatives and its antibacterial activities
topic Q Science (General)
url http://ir.unimas.my/id/eprint/18505/
http://ir.unimas.my/id/eprint/18505/
http://ir.unimas.my/id/eprint/18505/