Catalyst‐free, one‐pot three‐component synthesis of N,3‐diphenybenzoimidazothiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones)
The present work, highlights a highly effective unique procedure for the synthesis of N,3‐diphenybenzo[d]imidazo[2,1‐b]thiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones) via the one‐pot three‐component reaction between aryl glyoxal, aryl amine, and 2‐aminobenzothiazole under catalyst‐free condi...
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Veröffentlicht in: | Journal of heterocyclic chemistry 2023-05, Vol.60 (5), p.879-888 |
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container_title | Journal of heterocyclic chemistry |
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creator | Hajipour, Mina Mehrabi, Hossein |
description | The present work, highlights a highly effective unique procedure for the synthesis of N,3‐diphenybenzo[d]imidazo[2,1‐b]thiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones) via the one‐pot three‐component reaction between aryl glyoxal, aryl amine, and 2‐aminobenzothiazole under catalyst‐free conditions. The present mild and green method uses EtOH without catalyst at reflux conditions. No catalyst with high yields, availability of the starting materials, operational simplicity, cleaner reaction profile, no harmful byproducts, and the isolated products in pure form are the advantages of this protocol. Structures of all the freshly synthesized products have been deduced by their FT‐IR, 1H‐NMR, 13C‐NMR, and elemental analysis. |
doi_str_mv | 10.1002/jhet.4638 |
format | Article |
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The present mild and green method uses EtOH without catalyst at reflux conditions. No catalyst with high yields, availability of the starting materials, operational simplicity, cleaner reaction profile, no harmful byproducts, and the isolated products in pure form are the advantages of this protocol. 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The present mild and green method uses EtOH without catalyst at reflux conditions. No catalyst with high yields, availability of the starting materials, operational simplicity, cleaner reaction profile, no harmful byproducts, and the isolated products in pure form are the advantages of this protocol. Structures of all the freshly synthesized products have been deduced by their FT‐IR, 1H‐NMR, 13C‐NMR, and elemental analysis.</description><subject>Aminobenzothiazoles</subject><subject>Aromatic compounds</subject><subject>Catalysts</subject><subject>Chemical analysis</subject><subject>Chemical synthesis</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqNTUtOwzAQtRBIhM-CG1hi00pNa8dNm6wrECtWLLqrXDKRHSWekHEl0hVH6Bk5CVPBAVjMzPvpjRAPWs21UtmicRDny5UpLkSiy6VJc12aS5Gwl6U6z7bX4oaoYarNep2I08ZG244Uv79O9QAwkxiAcY9RRscC43fselZDlDSG6IA8Sazl68ywWfneQRj3EI7oO1_ZI0bnebdA0oZK4ue49zTR59JzsmWQ8Ux-me18wClEZwP_oOmduKptS3D_d2_F4_PT2-Yl7Qf8OADFXYOHIbC1ywq1KlSZa2P-l_oBKSRkHw</recordid><startdate>20230501</startdate><enddate>20230501</enddate><creator>Hajipour, Mina</creator><creator>Mehrabi, Hossein</creator><general>Wiley Subscription Services, Inc</general><scope/></search><sort><creationdate>20230501</creationdate><title>Catalyst‐free, one‐pot three‐component synthesis of N,3‐diphenybenzoimidazothiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones)</title><author>Hajipour, Mina ; Mehrabi, Hossein</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_28068095133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Aminobenzothiazoles</topic><topic>Aromatic compounds</topic><topic>Catalysts</topic><topic>Chemical analysis</topic><topic>Chemical synthesis</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hajipour, Mina</creatorcontrib><creatorcontrib>Mehrabi, Hossein</creatorcontrib><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hajipour, Mina</au><au>Mehrabi, Hossein</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Catalyst‐free, one‐pot three‐component synthesis of N,3‐diphenybenzoimidazothiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones)</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><date>2023-05-01</date><risdate>2023</risdate><volume>60</volume><issue>5</issue><spage>879</spage><epage>888</epage><pages>879-888</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>The present work, highlights a highly effective unique procedure for the synthesis of N,3‐diphenybenzo[d]imidazo[2,1‐b]thiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones) via the one‐pot three‐component reaction between aryl glyoxal, aryl amine, and 2‐aminobenzothiazole under catalyst‐free conditions. The present mild and green method uses EtOH without catalyst at reflux conditions. No catalyst with high yields, availability of the starting materials, operational simplicity, cleaner reaction profile, no harmful byproducts, and the isolated products in pure form are the advantages of this protocol. Structures of all the freshly synthesized products have been deduced by their FT‐IR, 1H‐NMR, 13C‐NMR, and elemental analysis.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/jhet.4638</doi></addata></record> |
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subjects | Aminobenzothiazoles Aromatic compounds Catalysts Chemical analysis Chemical synthesis NMR Nuclear magnetic resonance |
title | Catalyst‐free, one‐pot three‐component synthesis of N,3‐diphenybenzoimidazothiazoles and oxybis(1‐phenyl‐2‐(phenylamino)ethanones) |
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