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Simple and Efficient Microwave Assisted N-Alkylation of Isatin
We present herein the results of microwave promoted N-alkylations of isatin (1) with different alkyl, benzyl and functionalized alkyl halides. Reactions were carried out under different conditions, always employing methodologies compatible with MW assisted chemistry. Generation of isatin anion emplo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245312/ https://www.ncbi.nlm.nih.gov/pubmed/18463585 http://dx.doi.org/10.3390/molecules13040831 |
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author | Shmidt, María Sol Reverdito, Ana María Kremenchuzky, Lautaro Perillo, Isabel Amalia Blanco, María Mercedes |
author_facet | Shmidt, María Sol Reverdito, Ana María Kremenchuzky, Lautaro Perillo, Isabel Amalia Blanco, María Mercedes |
author_sort | Shmidt, María Sol |
collection | PubMed |
description | We present herein the results of microwave promoted N-alkylations of isatin (1) with different alkyl, benzyl and functionalized alkyl halides. Reactions were carried out under different conditions, always employing methodologies compatible with MW assisted chemistry. Generation of isatin anion employing diverse bases and solvents or using the preformed isatin sodium salt was tested. The best results were achieved using K(2)CO(3) or Cs(2)CO(3) and a few drops of N,N-dimethylformamide or N-methyl-2-pyrrolidinone. These reactions present noteworthy advantages over those carried out employing conventional heating. |
format | Online Article Text |
id | pubmed-6245312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62453122018-11-26 Simple and Efficient Microwave Assisted N-Alkylation of Isatin Shmidt, María Sol Reverdito, Ana María Kremenchuzky, Lautaro Perillo, Isabel Amalia Blanco, María Mercedes Molecules Article We present herein the results of microwave promoted N-alkylations of isatin (1) with different alkyl, benzyl and functionalized alkyl halides. Reactions were carried out under different conditions, always employing methodologies compatible with MW assisted chemistry. Generation of isatin anion employing diverse bases and solvents or using the preformed isatin sodium salt was tested. The best results were achieved using K(2)CO(3) or Cs(2)CO(3) and a few drops of N,N-dimethylformamide or N-methyl-2-pyrrolidinone. These reactions present noteworthy advantages over those carried out employing conventional heating. MDPI 2008-04-10 /pmc/articles/PMC6245312/ /pubmed/18463585 http://dx.doi.org/10.3390/molecules13040831 Text en © 2008 by MDPI(http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Article Shmidt, María Sol Reverdito, Ana María Kremenchuzky, Lautaro Perillo, Isabel Amalia Blanco, María Mercedes Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title | Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title_full | Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title_fullStr | Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title_full_unstemmed | Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title_short | Simple and Efficient Microwave Assisted N-Alkylation of Isatin |
title_sort | simple and efficient microwave assisted n-alkylation of isatin |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245312/ https://www.ncbi.nlm.nih.gov/pubmed/18463585 http://dx.doi.org/10.3390/molecules13040831 |
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