One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions

To develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic a...

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Detalles Bibliográficos
Autores principales: Li, Wei Lin, Wang, Li Li, Luo, Qiu Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683505/
https://www.ncbi.nlm.nih.gov/pubmed/23818828
http://dx.doi.org/10.1155/2013/702929
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author Li, Wei Lin
Wang, Li Li
Luo, Qiu Yan
author_facet Li, Wei Lin
Wang, Li Li
Luo, Qiu Yan
author_sort Li, Wei Lin
collection PubMed
description To develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic aldehydes (1 mmol), and 2-aminobenzothiazole (1 mmol) at 60°C under solvent-free conditions.
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spelling pubmed-36835052013-07-01 One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions Li, Wei Lin Wang, Li Li Luo, Qiu Yan ScientificWorldJournal Research Article To develop a new facile protocol for the synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthol derivatives, N-bromosuccinimide (NBS) was used as an efficient catalyst for the one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols in excellent yields from β-naphthol (1 mmol), aromatic aldehydes (1 mmol), and 2-aminobenzothiazole (1 mmol) at 60°C under solvent-free conditions. Hindawi Publishing Corporation 2013-05-30 /pmc/articles/PMC3683505/ /pubmed/23818828 http://dx.doi.org/10.1155/2013/702929 Text en Copyright © 2013 Wei Lin Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Wei Lin
Wang, Li Li
Luo, Qiu Yan
One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title_full One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title_fullStr One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title_full_unstemmed One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title_short One-Pot Synthesis of 2′-Aminobenzothiazolo-Arylmethyl-2-Naphthols Catalyzed by NBS under Solvent-Free Conditions
title_sort one-pot synthesis of 2′-aminobenzothiazolo-arylmethyl-2-naphthols catalyzed by nbs under solvent-free conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3683505/
https://www.ncbi.nlm.nih.gov/pubmed/23818828
http://dx.doi.org/10.1155/2013/702929
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