Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles

A highly efficient, eco-friendly and one-pot synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles was developed involving the reaction of 2-acetyl benzofurans and 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole in the presence of molecular iodine under ultrasonic conditions to give 5-(ben...

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Main Authors:	Kumar Surender, Sharma Dinesh Kumar
Format:	Article
Language:	English
Published:	De Gruyter 2017-02-01
Series:	Green Processing and Synthesis
Subjects:	5-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles 5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole microwave conditions ultrasonic conditions
Online Access:	https://doi.org/10.1515/gps-2016-0099

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record_format	Article
spelling	doaj-dae8d7994c324276be960e2b14b3fb572021-10-02T19:10:00ZengDe GruyterGreen Processing and Synthesis2191-95422191-95502017-02-0161737710.1515/gps-2016-0099Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazolesKumar Surender0Sharma Dinesh Kumar1Department of Chemistry, Technological Institute of Textile and Sciences, Bhiwani, 127021, IndiaDepartment of Chemistry, Kishanlal Public College, Rewari, 123401, IndiaA highly efficient, eco-friendly and one-pot synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles was developed involving the reaction of 2-acetyl benzofurans and 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole in the presence of molecular iodine under ultrasonic conditions to give 5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles, which was further cyclised using Eaton’s reagent under microwave conditions to give 5-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles.https://doi.org/10.1515/gps-2016-00995-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles5-mercapto-3-(4-chlorophenyl)-1,2,4triazolemicrowave conditionsultrasonic conditions
collection	DOAJ
language	English
format	Article
sources	DOAJ
author	Kumar Surender Sharma Dinesh Kumar
spellingShingle	Kumar Surender Sharma Dinesh Kumar Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles Green Processing and Synthesis 5-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles 5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole microwave conditions ultrasonic conditions
author_facet	Kumar Surender Sharma Dinesh Kumar
author_sort	Kumar Surender
title	Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
title_short	Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
title_full	Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
title_fullStr	Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
title_full_unstemmed	Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
title_sort	ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles
publisher	De Gruyter
series	Green Processing and Synthesis
issn	2191-9542 2191-9550
publishDate	2017-02-01
description	A highly efficient, eco-friendly and one-pot synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles was developed involving the reaction of 2-acetyl benzofurans and 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole in the presence of molecular iodine under ultrasonic conditions to give 5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles, which was further cyclised using Eaton’s reagent under microwave conditions to give 5-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles.
topic	5-(benzofuran-2-yl)-2-(4-chlorophenyl)thiazolo[3,2-b][1,2,4]triazoles 5-(benzofuran-2-yl)-acylthio-3-(4-chlorophenyl)-1,2,4triazoles 5-mercapto-3-(4-chlorophenyl)-1,2,4triazole microwave conditions ultrasonic conditions
url	https://doi.org/10.1515/gps-2016-0099
work_keys_str_mv	AT kumarsurender ultrasoundpromotedgreensynthesisofbenzofuransubstitutedthiazolo32b124triazoles AT sharmadineshkumar ultrasoundpromotedgreensynthesisofbenzofuransubstitutedthiazolo32b124triazoles
_version_	1716848155738243072

Ultrasound promoted green synthesis of benzofuran substituted thiazolo[3,2-b][1,2,4]triazoles

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