Síntese quimioenzimática do levetiracetam e análogos

Detalhes bibliográficos
Ano de defesa: 2015
Autor(a) principal: Amaral, Bruno Sérgio do [UNESP]
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Estadual Paulista (Unesp)
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/11449/124450
Resumo: Biocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium...
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spelling Síntese quimioenzimática do levetiracetam e análogosBiocatáliseSintese assimetricaMetaloenzimasEnantiomerosLíquidos iônicosAsymmetric synthesisBiocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium...Os biocatalisadores (enzimas e/ou micro-organismos) são amplamente utilizados na síntese de moléculas bioativas, em especial os fármacos, para gerar ou resolver centros quirais. O levetiracetam, comercialmente conhecido como Keppra®, é um composto quiral com propriedades anticonvulsivantes cuja atividade farmacológica está relacionada ao enantiômero (S). O aumento da opção pelo uso do levetiracetam em detrimento a outros fármacos anticonvulsivantes está intimamente associado à baixa ocorrência de efeitos colaterais provocados por este. Diversas rotas quimiossintéticas para sua produção são relatadas na literatura. A maioria delas envolve um elevado número de etapas, alto consumo energético, uso de catalisadores metálicos e baixos rendimentos globais. Em contrapartida, este projeto teve por objetivo empregar uma rota quimioenzimática, com menor número de etapas, condições mais brandas e ambientalmente amigáveis de reação para a síntese do levetiracetam e análogos (série alifática). A respectiva série aromática também foi sintetizada, uma vez que trata-se de blocos construtores quirais para a síntese de compostos com reconhecida atividade anti-malária. A primeira etapa consistiu na síntese das cianidrinas racêmicas seguida da substiuição da hidroxila destas por heterociclos nitrogenados. Uma coleção de enzimas do tipo nitrila hidratases (E.C. 4.2.1.84) foi empregada para catalisar a conversão das nitrilas α-substituidas por N-heterociclos nas respectivas amidas quirais. As enzimas foram utilizadas tanto na forma isolada (obtidas comercialmente) quanto em células íntegras de bactérias e leveduras da Coleção de Micro-organismos do Laboratório de Biocatálise do IQ-UNESP Araraquara. As reações enzimáticas foram conduzidas em meio aquoso tamponado e em sistemas binários líquido iônico : solução tampão (10, 20, 40 e 80%) a fim de avaliar a influência do...Universidade Estadual Paulista (Unesp)Milagre, Cintia Duarte de Freitas [UNESP]Universidade Estadual Paulista (Unesp)Amaral, Bruno Sérgio do [UNESP]2015-07-13T12:10:18Z2015-07-13T12:10:18Z2015-02-23info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis212 f. : il. -application/pdfAMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015.http://hdl.handle.net/11449/124450000825064000825064.pdf33004030072P833004030072P814257489168493760000-0001-5627-8616Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2025-05-28T11:23:55Zoai:repositorio.unesp.br:11449/124450Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-28T11:23:55Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Síntese quimioenzimática do levetiracetam e análogos
title Síntese quimioenzimática do levetiracetam e análogos
spellingShingle Síntese quimioenzimática do levetiracetam e análogos
Amaral, Bruno Sérgio do [UNESP]
Biocatálise
Sintese assimetrica
Metaloenzimas
Enantiomeros
Líquidos iônicos
Asymmetric synthesis
title_short Síntese quimioenzimática do levetiracetam e análogos
title_full Síntese quimioenzimática do levetiracetam e análogos
title_fullStr Síntese quimioenzimática do levetiracetam e análogos
title_full_unstemmed Síntese quimioenzimática do levetiracetam e análogos
title_sort Síntese quimioenzimática do levetiracetam e análogos
author Amaral, Bruno Sérgio do [UNESP]
author_facet Amaral, Bruno Sérgio do [UNESP]
author_role author
dc.contributor.none.fl_str_mv Milagre, Cintia Duarte de Freitas [UNESP]
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Amaral, Bruno Sérgio do [UNESP]
dc.subject.por.fl_str_mv Biocatálise
Sintese assimetrica
Metaloenzimas
Enantiomeros
Líquidos iônicos
Asymmetric synthesis
topic Biocatálise
Sintese assimetrica
Metaloenzimas
Enantiomeros
Líquidos iônicos
Asymmetric synthesis
description Biocatalysts (enzymes and/or microorganisms) are widely used in the synthesis of bioactive molecules, in particular pharmaceuticals, to generate or resolve chiral centers. Levetiracetam, commercially known as Keppra®, is a chiral compound with anticonvulsant properties whose pharmacological activity is related to the (S)-enantiomer. The increase in option for the use of levetiracetam over the others anticonvulsant drugs is closely associated with low incidence of side effects caused by this. Several chemosynthetic routes for its production are reported in the literature. Most of them involve numerous synthetic steps, high energy consumption, use of metal catalysts and low overall yields. On the other hand, this project aims to develop a chemoenzymatic route, with fewer steps, milder conditions and environmentally friendly reaction for the synthesis of levetiracetam and analogues (aliphatic series). The respective aromatic series was also synthesized, since it is chiral building blocks for the synthesis of compounds with known antimalarial activity. The first step was the synthesis of racemic cyanohydrin followed by substitution of the hydroxyl group by nitrogen heterocycles. Collections of nitrile hydratase enzymes type (EC 4.2.1.84) were used to catalyze the conversion of N-heterocycles α-substituted nitriles in the respective chiral amides. The enzymes were used both in isolated form (obtained commercially) as in whole cells bacteria and yeast Collection of Microorganisms of Biocatalysis Laboratory of IQ-UNESP Araraquara. The enzymatic reactions were performed in buffered aqueous medium and ionic liquid : buffer (10, 20, 40 and 80%) binary systems in order to evaluate the influence of the solvent on the enantioselectivity and yield of these reactions. The ionic liquids synthesized and used in this work were 1-butyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium...
publishDate 2015
dc.date.none.fl_str_mv 2015-07-13T12:10:18Z
2015-07-13T12:10:18Z
2015-02-23
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv AMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015.
http://hdl.handle.net/11449/124450
000825064
000825064.pdf
33004030072P8
33004030072P8
1425748916849376
0000-0001-5627-8616
identifier_str_mv AMARAL, Bruno Sérgio do. Síntese quimioenzimática do levetiracetam e análogos. 2015. 212 f. Dissertação (mestrado) - Universidade Estadual Paulista, Instituto de Química, 2015.
000825064
000825064.pdf
33004030072P8
1425748916849376
0000-0001-5627-8616
url http://hdl.handle.net/11449/124450
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 212 f. : il. -
application/pdf
dc.publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.source.none.fl_str_mv Aleph
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
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instname_str Universidade Estadual Paulista (UNESP)
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reponame_str Repositório Institucional da UNESP
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