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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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. |
format | Online Article Text |
id | pubmed-9078240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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