Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines

A systematic study on the condensation reaction of 2,4-dichlorobenzo[h]quinoline and naphth-1-ylamine in the presence of CuI as catalyst to functionalised mono- and di-substituted (naphthalen-1-yl)benzo[h]quinoline amines was described. Subsequently these mono- and di-substituted amines on polyphosp...

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Detalles Bibliográficos
Autores principales: Prabha, Kolandaivel, Rajendra Prasad, K.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506974/
https://www.ncbi.nlm.nih.gov/pubmed/26199754
http://dx.doi.org/10.1016/j.jare.2014.02.007
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author Prabha, Kolandaivel
Rajendra Prasad, K.J.
author_facet Prabha, Kolandaivel
Rajendra Prasad, K.J.
author_sort Prabha, Kolandaivel
collection PubMed
description A systematic study on the condensation reaction of 2,4-dichlorobenzo[h]quinoline and naphth-1-ylamine in the presence of CuI as catalyst to functionalised mono- and di-substituted (naphthalen-1-yl)benzo[h]quinoline amines was described. Subsequently these mono- and di-substituted amines on polyphosphoric acid catalysed cyclisation reaction with aromatic/heteroaromatic carboxylic acids led to the construction of angular and linear aromatic/heteroaromatic substituted dinaphthonaphthyridines in good yields.
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spelling pubmed-45069742015-07-21 Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines Prabha, Kolandaivel Rajendra Prasad, K.J. J Adv Res Original Article A systematic study on the condensation reaction of 2,4-dichlorobenzo[h]quinoline and naphth-1-ylamine in the presence of CuI as catalyst to functionalised mono- and di-substituted (naphthalen-1-yl)benzo[h]quinoline amines was described. Subsequently these mono- and di-substituted amines on polyphosphoric acid catalysed cyclisation reaction with aromatic/heteroaromatic carboxylic acids led to the construction of angular and linear aromatic/heteroaromatic substituted dinaphthonaphthyridines in good yields. Elsevier 2015-07 2014-03-05 /pmc/articles/PMC4506974/ /pubmed/26199754 http://dx.doi.org/10.1016/j.jare.2014.02.007 Text en © 2014 Production and hosting by Elsevier B.V. on behalf of Cairo University. https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Original Article
Prabha, Kolandaivel
Rajendra Prasad, K.J.
Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title_full Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title_fullStr Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title_full_unstemmed Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title_short Benzoquinoline amines – Key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
title_sort benzoquinoline amines – key intermediates for the synthesis of angular and linear dinaphthonaphthyridines
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506974/
https://www.ncbi.nlm.nih.gov/pubmed/26199754
http://dx.doi.org/10.1016/j.jare.2014.02.007
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