Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives

Amidoalkylation of secondary heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-chloroacetamide resulted the new compounds 5-10 that contain 1,3,4-thiadiazole-5-thione moiety alongside pyperidine, morpholine, and cytisine fragments. In vitro screening of antimicrobial activit...

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Main Authors: Turdibek Toshmurodov, Abdukhakim Ziyaev, Sobirdjan Sasmakov, Jaloliddin Abdurakhmanov, Mavluda Ziyaeva, Dilnoza Ismailova, Shakhnoz Azimova
Format: Article
Language:English
Published: Growing Science 2021-01-01
Series:Current Chemistry Letters
Online Access:http://www.growingscience.com/ccl/Vol10/ccl_2021_21.pdf
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author Turdibek Toshmurodov
Abdukhakim Ziyaev
Sobirdjan Sasmakov
Jaloliddin Abdurakhmanov
Mavluda Ziyaeva
Dilnoza Ismailova
Shakhnoz Azimova
author_facet Turdibek Toshmurodov
Abdukhakim Ziyaev
Sobirdjan Sasmakov
Jaloliddin Abdurakhmanov
Mavluda Ziyaeva
Dilnoza Ismailova
Shakhnoz Azimova
author_sort Turdibek Toshmurodov
collection DOAJ
description Amidoalkylation of secondary heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-chloroacetamide resulted the new compounds 5-10 that contain 1,3,4-thiadiazole-5-thione moiety alongside pyperidine, morpholine, and cytisine fragments. In vitro screening of antimicrobial activity of synthesized compounds showed that N-[5-(amylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-morpholinacetamide exhibited an appreciable antibacterial activity against gram-negative bacteria of Escherichia coli (inhibition zone diameter of 16 mm) and gram-positive bacteria of Staphylococcus aureus and Bacillus subtilis (10-13 mm).
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spelling doaj.art-bcb8b005f02548c6b094e445a4ddeabc2022-12-22T00:07:35ZengGrowing ScienceCurrent Chemistry Letters1927-72961927-730X2021-01-0110442743410.5267/j.ccl.2021.5.002Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivativesTurdibek ToshmurodovAbdukhakim ZiyaevSobirdjan SasmakovJaloliddin AbdurakhmanovMavluda ZiyaevaDilnoza IsmailovaShakhnoz AzimovaAmidoalkylation of secondary heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-chloroacetamide resulted the new compounds 5-10 that contain 1,3,4-thiadiazole-5-thione moiety alongside pyperidine, morpholine, and cytisine fragments. In vitro screening of antimicrobial activity of synthesized compounds showed that N-[5-(amylsulfanyl)-1,3,4-thiadiazol-2-yl]-2'-morpholinacetamide exhibited an appreciable antibacterial activity against gram-negative bacteria of Escherichia coli (inhibition zone diameter of 16 mm) and gram-positive bacteria of Staphylococcus aureus and Bacillus subtilis (10-13 mm).http://www.growingscience.com/ccl/Vol10/ccl_2021_21.pdf
spellingShingle Turdibek Toshmurodov
Abdukhakim Ziyaev
Sobirdjan Sasmakov
Jaloliddin Abdurakhmanov
Mavluda Ziyaeva
Dilnoza Ismailova
Shakhnoz Azimova
Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
Current Chemistry Letters
title Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
title_full Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
title_fullStr Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
title_full_unstemmed Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
title_short Amidoalkylation of heterocyclic amines by N-[5-(alkylsulfanyl)-1,3,4-thiadiazol-2-yl]- 2'-chloroacetamide and antimicrobial activity of derivatives
title_sort amidoalkylation of heterocyclic amines by n 5 alkylsulfanyl 1 3 4 thiadiazol 2 yl 2 chloroacetamide and antimicrobial activity of derivatives
url http://www.growingscience.com/ccl/Vol10/ccl_2021_21.pdf
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