An economical and practical procedure of favipiravir synthesis for the treatment of Covid-19

dc.authorid0000-0002-7577-0320
dc.authorid0000-0002-1423-0435
dc.contributor.authorKarataş, Hacer
dc.contributor.authorHanashalshahaby, Essam Hamied Ahmed
dc.contributor.authorÇatal, Ünal
dc.contributor.authorBütün, Yaşar Enes
dc.contributor.authorKurt, Elif
dc.contributor.authorGürsel, Şahin
dc.contributor.authorKaya, Adil
dc.contributor.authorGüzel, Mustafa
dc.date.accessioned2023-10-05T06:55:10Z
dc.date.available2023-10-05T06:55:10Z
dc.date.issued2023
dc.departmentİstanbul Medipol Üniversitesi, Eczacılık Fakültesi, Eczacılık Meslek Bilimleri Bölümü, Farmasötik Kimya Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Rektörlük, Sağlık Bilim ve Teknolojileri Araştırma Enstitüsü
dc.departmentİstanbul Medipol Üniversitesi, Eczacılık Fakültesi, Eczacılık Meslek Bilimleri Bölümü, Klinik Eczacılık Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Sağlık Bilimleri Enstitüsü, Moleküler Tıp ve Biyoteknoloji Ana Bilim Dalı
dc.departmentİstanbul Medipol Üniversitesi, Uluslararası Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Farmakoloji Ana Bilim Dalı
dc.description.abstractFavipiravir is a wide-spectrum antiviral generic drug that has received large attention during the recent COVID-19 pandemic. While there are synthetic strategies for favipiravir synthesis, economical procedures could contribute to industrial scale synthesis and availability. Accordingly, our efforts focused on an economic and scalable procedure for favipiravir synthesis via the 3,6-dichloropyrazine-2-carbonitrile intermediate obtained from 3-aminopyrazine-2-carboxylic acid. The process afforded favipiravir with 43% yield (from 3,6-dichloropyrazine-2-carbonitrile, by fluorination, hydroxylation, and nitrile hydrolysis reactions) and greater than 99% purity without a chromatographic purification step. Graphical abstract: [Figure not available: see fulltext.]
dc.description.sponsorshipATABAY Fine Chemicals and Pharmaceutical Companyen_US
dc.identifier.citationKarataş, H., Hanashalshahaby, E. H. A., Çatal, Ü., Bütün, Y. E., Kurt, E., Gürsel, Ş. ... Güzel, M. (2023). An economical and practical procedure of favipiravir synthesis for the treatment of Covid-19. Chemical Papers, 77(3), 1695-1702. https://doi.org/10.1007/s11696-022-02595-1
dc.identifier.doi10.1007/s11696-022-02595-1
dc.identifier.endpage1702
dc.identifier.issn0366-6352
dc.identifier.issn2585-7290
dc.identifier.issue3
dc.identifier.pmid36466109
dc.identifier.scopus2-s2.0-85142345509
dc.identifier.scopusqualityQ2
dc.identifier.startpage1695
dc.identifier.urihttps://doi.org/10.1007/s11696-022-02595-1
dc.identifier.urihttps://hdl.handle.net/20.500.12511/11522
dc.identifier.volume77
dc.identifier.wos000886743800001en_US
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.institutionauthorKarataş, Hacer
dc.institutionauthorBütün, Yaşar Enes
dc.institutionauthorGüzel, Mustafa
dc.language.isoen
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.relation.ispartofChemical Papersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.relation.tubitakinfo:eu-repo/grantAgreement/TUBITAK/SOBAG/18AG020
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectFavipiravir Synthesis
dc.subject3,6-Dichloropyrazine-2-Carbonitrile
dc.subjectCovid-19 Treatment
dc.subjectProcess Development
dc.subjectActive Pharmaceutical Ingredient (API) Synthesis
dc.titleAn economical and practical procedure of favipiravir synthesis for the treatment of Covid-19
dc.typeArticle

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