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An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position

A facile synthetic procedure for the production of N-alkylated 3,4-dihydroisoquinolinone derivatives is described. The desired products were obtained by N-alkylation of 3,3′-dimethyl-3,4-dihydroisoquinoline derivatives followed by oxidation of the resulting iminium salts. Reaction conditions for bot...

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Detalles Bibliográficos
Autores principales: Tazawa, Aoi, Ando, Junki, Ishizawa, Kohei, Azumaya, Isao, Hikawa, Hidemasa, Tanaka, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078240/
https://www.ncbi.nlm.nih.gov/pubmed/35539622
http://dx.doi.org/10.1039/c7ra13627g
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author Tazawa, Aoi
Ando, Junki
Ishizawa, Kohei
Azumaya, Isao
Hikawa, Hidemasa
Tanaka, Minoru
author_facet Tazawa, Aoi
Ando, Junki
Ishizawa, Kohei
Azumaya, Isao
Hikawa, Hidemasa
Tanaka, Minoru
author_sort Tazawa, Aoi
collection PubMed
description A facile synthetic procedure for the production of N-alkylated 3,4-dihydroisoquinolinone derivatives is described. The desired products were obtained by N-alkylation of 3,3′-dimethyl-3,4-dihydroisoquinoline derivatives followed by oxidation of the resulting iminium salts. Reaction conditions for both steps were very mild and the desired cyclization products could be obtained in good yield. This strategy allows the generation of N-substituted 3,4-dihydroisoquinolinone derivatives with substituents at the 3-position.
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spelling pubmed-90782402022-05-09 An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position Tazawa, Aoi Ando, Junki Ishizawa, Kohei Azumaya, Isao Hikawa, Hidemasa Tanaka, Minoru RSC Adv Chemistry A facile synthetic procedure for the production of N-alkylated 3,4-dihydroisoquinolinone derivatives is described. The desired products were obtained by N-alkylation of 3,3′-dimethyl-3,4-dihydroisoquinoline derivatives followed by oxidation of the resulting iminium salts. Reaction conditions for both steps were very mild and the desired cyclization products could be obtained in good yield. This strategy allows the generation of N-substituted 3,4-dihydroisoquinolinone derivatives with substituents at the 3-position. The Royal Society of Chemistry 2018-02-07 /pmc/articles/PMC9078240/ /pubmed/35539622 http://dx.doi.org/10.1039/c7ra13627g Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tazawa, Aoi
Ando, Junki
Ishizawa, Kohei
Azumaya, Isao
Hikawa, Hidemasa
Tanaka, Minoru
An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title_full An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title_fullStr An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title_full_unstemmed An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title_short An efficient route to N-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
title_sort efficient route to n-alkylated 3,4-dihydroisoquinolinones with substituents at the 3-position
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078240/
https://www.ncbi.nlm.nih.gov/pubmed/35539622
http://dx.doi.org/10.1039/c7ra13627g
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