Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos

Detalhes bibliográficos
Ano de defesa: 2016
Autor(a) principal: Delling, Felix Nicolai
Orientador(a): Schpector, Júlio Zukerman lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Câmpus São Carlos
Programa de Pós-Graduação: Programa de Pós-Graduação em Química - PPGQ
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/20.500.14289/10216
Resumo: Using techniques/procedures of green chemistry, solid state grinding, solvent drop grinding and solvent drop grinding with heating, twenty compounds were synthesized. Eleven compounds of dropropizine (antitussive): two co-crystals and nine co-crystal salts, nine compounds of carbamazepine (anticonvulsant and mood stabilizer) were synthesized: eigth channel compounds and a possible co-crystal. The sulfamethoxazole (bactericidal) showed not to be a good choice as no new compounds could be synthesized in the reaction conditions used for all experiments, only its hemihydrate could be obtained. The compounds were characterized by powder X-ray diffraction, infrared spectroscopy, differential scanning calorimetry, mass spectrometry and single crystal X-ray diffraction methods. Using infrared spectroscopy it was possible to identify four characteristic vibrational modes for the salts, i.e. two vibrational modes of the COO- species (~1540 and ~1358 cm-1) and two of the N+–H species (~1385 and ~1258 cm-1). For the co-crystals the characteristic stretch of the carboxylic acids, at ~1700cm-1, did not disappear. The crystal, molecular and packing structures of two compounds, i.e. of the sulfamethoxazole hemihydrate and of the salt of dropropizine with 4-hydroxybenzoic acid, were determined by single crystal X-ray diffraction. Mechanisms were proposed for the solid state grinding and solvent drop grinding with heating reactions. Finally, a proton transfer mechanism was proposed for the solid state grinding and solvent drop grinding with heating to synthesize a salt.
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spelling Delling, Felix NicolaiSchpector, Júlio Zukermanhttp://lattes.cnpq.br/4252331837170383http://lattes.cnpq.br/63524109195560629df4d7f5-cf1b-42d7-a530-07a871dfd6392018-06-25T20:03:06Z2018-06-25T20:03:06Z2016-02-29DELLING, Felix Nicolai. Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/10216.https://repositorio.ufscar.br/handle/20.500.14289/10216Using techniques/procedures of green chemistry, solid state grinding, solvent drop grinding and solvent drop grinding with heating, twenty compounds were synthesized. Eleven compounds of dropropizine (antitussive): two co-crystals and nine co-crystal salts, nine compounds of carbamazepine (anticonvulsant and mood stabilizer) were synthesized: eigth channel compounds and a possible co-crystal. The sulfamethoxazole (bactericidal) showed not to be a good choice as no new compounds could be synthesized in the reaction conditions used for all experiments, only its hemihydrate could be obtained. The compounds were characterized by powder X-ray diffraction, infrared spectroscopy, differential scanning calorimetry, mass spectrometry and single crystal X-ray diffraction methods. Using infrared spectroscopy it was possible to identify four characteristic vibrational modes for the salts, i.e. two vibrational modes of the COO- species (~1540 and ~1358 cm-1) and two of the N+–H species (~1385 and ~1258 cm-1). For the co-crystals the characteristic stretch of the carboxylic acids, at ~1700cm-1, did not disappear. The crystal, molecular and packing structures of two compounds, i.e. of the sulfamethoxazole hemihydrate and of the salt of dropropizine with 4-hydroxybenzoic acid, were determined by single crystal X-ray diffraction. Mechanisms were proposed for the solid state grinding and solvent drop grinding with heating reactions. Finally, a proton transfer mechanism was proposed for the solid state grinding and solvent drop grinding with heating to synthesize a salt.Utilizando técnicas/procedimentos de química sustentável (moagem no estado sólido, moagem com gotas de solvente e moagem com gotas de solvente e aquecimento), foram sintetizados onze compostos com dropropizina (antitussígeno) sendo dois cocristais e nove sais-cocristais, nove compostos de carbamazepina (anticonvulsivo e estabilizador do humor) sendo oito compostos de canal e um possível cocristal. O sulfametoxazol (bactericida) mostrou não ter sido uma boa escolha nas condições reacionais utilizadas em todos os experimentos, somente pode ser obtido o hemihidrato. Os compostos foram caracterizados utilizando os métodos de difração de raio X de pó, espectroscopia de infravermelho, calorimetria diferencial de varredura, espectrometria de massa, microscopia eletrônica de varredura e difração de raio X de monocristal. Utilizando espectroscopia de infravermelho foram identificados quatro modos vibracionais característicos dos saiscocristais, sendo dois modos vibracionais relacionados com a espécie COO– (~1540 e ~1358 cm-1) e outros dois relacionados com a espécie N+–H (~1385 e ~1258 cm-1). No caso dos cocristais, o estiramento característico dos ácidos carboxílicos, em ~1700 cm-1, não desaparecem. Por difração de raio X de monocristal foram determinadas as estruturas cristalinas e moleculares de dois compostos (do sulfametoxazol hemihidratado e do sal-cocristal de dropropizina com ácido 4- hidroxibenzoico). Para as sínteses utilizando moagem no estado sólido e moagem com gotas de solvente foram propostos mecanismos reacionais. Finalmente, num caso de moagem com gotas de solvente no qual se forma um sal-cocristal, propomos um mecanismo para a transferência de prótons.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)porUniversidade Federal de São CarlosCâmpus São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarQuímica inorgânicaSínteseChemistry, InorganicSynthesisCIENCIAS EXATAS E DA TERRA::QUIMICASíntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativosSynthesis, characterization of co-crystals and salts of active pharmaceutical ingredientsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisOnline600600e0a7cf72-f4fb-48f4-93c2-3e7bc492b3cbinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINALTeseFND.pdfTeseFND.pdfapplication/pdf13643399https://repositorio.ufscar.br/bitstreams/a2e18259-9a41-485c-a965-538a32ad6e10/downloadc6168e0b5472be4454301e39e941cc25MD51trueAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81957https://repositorio.ufscar.br/bitstreams/5233265b-4542-4b5c-95b4-9baeef73e798/downloadae0398b6f8b235e40ad82cba6c50031dMD52falseAnonymousREADTEXTTeseFND.pdf.txtTeseFND.pdf.txtExtracted texttext/plain428931https://repositorio.ufscar.br/bitstreams/e4206bf2-dbf1-4bb9-b8fe-4b1e93155988/downloadce4bad5ebd2fa6c444cd0be08a6c7c13MD55falseAnonymousREADTHUMBNAILTeseFND.pdf.jpgTeseFND.pdf.jpgIM Thumbnailimage/jpeg6865https://repositorio.ufscar.br/bitstreams/cca65b7f-bcc1-42db-99ab-03884bb3bb36/downloadb7e588ee6f8c488068df4a51f3047cbfMD56falseAnonymousREAD20.500.14289/102162025-02-05 19:08:21.953Acesso abertoopen.accessoai:repositorio.ufscar.br:20.500.14289/10216https://repositorio.ufscar.brRepositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestrepositorio.sibi@ufscar.bropendoar:43222025-02-05T22:08:21Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)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
dc.title.por.fl_str_mv Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
dc.title.alternative.eng.fl_str_mv Synthesis, characterization of co-crystals and salts of active pharmaceutical ingredients
title Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
spellingShingle Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
Delling, Felix Nicolai
Química inorgânica
Síntese
Chemistry, Inorganic
Synthesis
CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
title_full Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
title_fullStr Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
title_full_unstemmed Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
title_sort Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos
author Delling, Felix Nicolai
author_facet Delling, Felix Nicolai
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/6352410919556062
dc.contributor.author.fl_str_mv Delling, Felix Nicolai
dc.contributor.advisor1.fl_str_mv Schpector, Júlio Zukerman
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4252331837170383
dc.contributor.authorID.fl_str_mv 9df4d7f5-cf1b-42d7-a530-07a871dfd639
contributor_str_mv Schpector, Júlio Zukerman
dc.subject.por.fl_str_mv Química inorgânica
Síntese
topic Química inorgânica
Síntese
Chemistry, Inorganic
Synthesis
CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.eng.fl_str_mv Chemistry, Inorganic
Synthesis
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA
description Using techniques/procedures of green chemistry, solid state grinding, solvent drop grinding and solvent drop grinding with heating, twenty compounds were synthesized. Eleven compounds of dropropizine (antitussive): two co-crystals and nine co-crystal salts, nine compounds of carbamazepine (anticonvulsant and mood stabilizer) were synthesized: eigth channel compounds and a possible co-crystal. The sulfamethoxazole (bactericidal) showed not to be a good choice as no new compounds could be synthesized in the reaction conditions used for all experiments, only its hemihydrate could be obtained. The compounds were characterized by powder X-ray diffraction, infrared spectroscopy, differential scanning calorimetry, mass spectrometry and single crystal X-ray diffraction methods. Using infrared spectroscopy it was possible to identify four characteristic vibrational modes for the salts, i.e. two vibrational modes of the COO- species (~1540 and ~1358 cm-1) and two of the N+–H species (~1385 and ~1258 cm-1). For the co-crystals the characteristic stretch of the carboxylic acids, at ~1700cm-1, did not disappear. The crystal, molecular and packing structures of two compounds, i.e. of the sulfamethoxazole hemihydrate and of the salt of dropropizine with 4-hydroxybenzoic acid, were determined by single crystal X-ray diffraction. Mechanisms were proposed for the solid state grinding and solvent drop grinding with heating reactions. Finally, a proton transfer mechanism was proposed for the solid state grinding and solvent drop grinding with heating to synthesize a salt.
publishDate 2016
dc.date.issued.fl_str_mv 2016-02-29
dc.date.accessioned.fl_str_mv 2018-06-25T20:03:06Z
dc.date.available.fl_str_mv 2018-06-25T20:03:06Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.citation.fl_str_mv DELLING, Felix Nicolai. Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/10216.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/20.500.14289/10216
identifier_str_mv DELLING, Felix Nicolai. Síntese, caracterização de cocristais e sais-cocristais de ingredientes farmacêuticos ativos. 2016. Tese (Doutorado em Química) – Universidade Federal de São Carlos, São Carlos, 2016. Disponível em: https://repositorio.ufscar.br/handle/20.500.14289/10216.
url https://repositorio.ufscar.br/handle/20.500.14289/10216
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Câmpus São Carlos
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