SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE

Favipiravir is a compound that appear to be one of pyrazine analogue that can act as Active Pharmaceutical Ingredients (API) and have been used as antiviral caused by Zika virus, Ebola virus, including SARS-CoV-2. The demand of favipiravir demand has been increased due to high cases of SARS-Co...

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Main Author: Lokitha, Angela
Format: Final Project
Language:Indonesia
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Online Access:https://digilib.itb.ac.id/gdl/view/82860
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Institution: Institut Teknologi Bandung
Language: Indonesia
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spelling id-itb.:828602024-07-22T11:25:05ZSYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE Lokitha, Angela Kimia Indonesia Final Project avipiravir, antiviral, 3-hydroxypyrazine-2-carboxamide, Selectfluor®, fluorination INSTITUT TEKNOLOGI BANDUNG https://digilib.itb.ac.id/gdl/view/82860 Favipiravir is a compound that appear to be one of pyrazine analogue that can act as Active Pharmaceutical Ingredients (API) and have been used as antiviral caused by Zika virus, Ebola virus, including SARS-CoV-2. The demand of favipiravir demand has been increased due to high cases of SARS-CoV-2 epidemic spread. Favipiravir play a big role as RNA-dependent RNA polymerase (RdRp) inhibitor which impactful by obstruct the growth of new virus. Various synthesis methods and routes have been developed with changes in stages, precursors, and conditions to determine the optimum condition of favipiravir synthesis method. In this experiment, optimization was conducted by deduct the reaction stages to one step, which is the fluorination of 3-hydroxypyrazine-2-carboxamide using Selectfluor®. Various reaction conditions were also varied to obtain conditions that could yield the optimum product yield. Thus, the favipiravir synthesis method can be carried out by reducing energy requirements, waste production, time, and being more economical. Synthesis of favipiravir derivative compounds is also carried out to improve modification of pyrazine widely developed as drugs, so structural analysis and effectiveness of new pyrazine compounds need to be conducted. The synthesized compound will then be characterized using 1H-NMR and 13C-NMR as well as 2D NMR. The yield value of the optimized synthesis of favipiravir compounds is determined by High Pressure Liquid Chromatography (HPLC) yield method and the highest HPLC yield value obtained is 23.41% out of 18 variations of reaction condition. In this research, five (5) favipiravir derivative that substituted at C-6 resulting in ether groups have been produced, which consist of one new compound and four compounds that previously have been reported text
institution Institut Teknologi Bandung
building Institut Teknologi Bandung Library
continent Asia
country Indonesia
Indonesia
content_provider Institut Teknologi Bandung
collection Digital ITB
language Indonesia
topic Kimia
spellingShingle Kimia
Lokitha, Angela
SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
description Favipiravir is a compound that appear to be one of pyrazine analogue that can act as Active Pharmaceutical Ingredients (API) and have been used as antiviral caused by Zika virus, Ebola virus, including SARS-CoV-2. The demand of favipiravir demand has been increased due to high cases of SARS-CoV-2 epidemic spread. Favipiravir play a big role as RNA-dependent RNA polymerase (RdRp) inhibitor which impactful by obstruct the growth of new virus. Various synthesis methods and routes have been developed with changes in stages, precursors, and conditions to determine the optimum condition of favipiravir synthesis method. In this experiment, optimization was conducted by deduct the reaction stages to one step, which is the fluorination of 3-hydroxypyrazine-2-carboxamide using Selectfluor®. Various reaction conditions were also varied to obtain conditions that could yield the optimum product yield. Thus, the favipiravir synthesis method can be carried out by reducing energy requirements, waste production, time, and being more economical. Synthesis of favipiravir derivative compounds is also carried out to improve modification of pyrazine widely developed as drugs, so structural analysis and effectiveness of new pyrazine compounds need to be conducted. The synthesized compound will then be characterized using 1H-NMR and 13C-NMR as well as 2D NMR. The yield value of the optimized synthesis of favipiravir compounds is determined by High Pressure Liquid Chromatography (HPLC) yield method and the highest HPLC yield value obtained is 23.41% out of 18 variations of reaction condition. In this research, five (5) favipiravir derivative that substituted at C-6 resulting in ether groups have been produced, which consist of one new compound and four compounds that previously have been reported
format Final Project
author Lokitha, Angela
author_facet Lokitha, Angela
author_sort Lokitha, Angela
title SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
title_short SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
title_full SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
title_fullStr SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
title_full_unstemmed SYNTHESIS OF FAVIPIRAVIR AND ITS DERIVATIVES FROM 3-HYDROXYPIRAZINE-2-CARBOXAMIDE
title_sort synthesis of favipiravir and its derivatives from 3-hydroxypirazine-2-carboxamide
url https://digilib.itb.ac.id/gdl/view/82860
_version_ 1822009892918001664