( E )- N’ -(1-(Benzofuran-2-yl)ethylidene)-1-(4-Methoxyphenyl)-5-Methyl-1 H -1,2,3-Triazole-4-Carbohydrazide

Abdel-Wahab, Bakr F., Bekheit, Mohamed S., Kariuki, Benson M. ORCID: https://orcid.org/0000-0002-8658-3897 and El-Hiti, Gamal A. ORCID: https://orcid.org/0000-0001-6675-3126 2023. ( E )- N’ -(1-(Benzofuran-2-yl)ethylidene)-1-(4-Methoxyphenyl)-5-Methyl-1 H -1,2,3-Triazole-4-Carbohydrazide. Molbank 2023 (2) , M1657. 10.3390/m1657

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Abstract

The reaction of equimolar equivalents of 1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbohydrazide (1) and 2-acetylbenzofuran (2) in anhydrous ethanol containing a catalytic amount of concentrated hydrochloric acid under reflux for 2 h gave (E)-N’-(1-(benzofuran-2-yl)ethylidene)-1-(4-methoxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carbohydrazide (3) in 86% yield. The structure of the title heterocycle 3 was confirmed using nuclear magnetic resonance and X-ray diffraction.

Item Type:	Article
Date Type:	Published Online
Status:	Published
Schools:	Chemistry
Additional Information:	License information from Publisher: LICENSE 1: URL: https://creativecommons.org/licenses/by/4.0/, Type: open-access
Publisher:	MDPI
Date of First Compliant Deposit:	10 July 2023
Date of Acceptance:	1 June 2023
Last Modified:	11 Jul 2023 01:30
URI:	https://orca.cardiff.ac.uk/id/eprint/160893

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