Methods of synthesizing a prostacyclin analog

The present invention provides processes for preparing a prostacyclin analogue of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R10 is a linear or branched C1-6 alkyl. The processes of the present invention comprise steps that generate improved yields and fewer byproducts than t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Chambournier, Gilles, Hering, Kirk William, Endres, Gregory William, Fedij, Victor, Krell, Mahmoud, Hussein Mahmoud
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Chambournier, Gilles
Hering, Kirk William
Endres, Gregory William
Fedij, Victor
Krell
Mahmoud, Hussein Mahmoud
description The present invention provides processes for preparing a prostacyclin analogue of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R10 is a linear or branched C1-6 alkyl. The processes of the present invention comprise steps that generate improved yields and fewer byproducts than traditional methods. The processes of the present invention employ reagents (e.g., the oxidizing reagent) that are less toxic that those used in the traditional methods (e.g., oxalyl chloride). Many of the processes of the present invention generate intermediates with improved e.e. and chemical purity; thereby eliminating the need of additional chromatography steps. And, the processes of the present invention are scalable to generate commercial quantities of the final compound.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_NZ708130A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>NZ708130A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_NZ708130A3</originalsourceid><addsrcrecordid>eNrjZND1TS3JyE8pVshPUyiuzCvJSC3OrMrMS1dIVCgoyi8uSUyuTM7JzFNIzEvMyU_nYWBNS8wpTuWF0twMcm6uIc4euqkF-fGpxQWJyal5qSXxflHmBhaGxgaOxgQVAAD6UClo</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Methods of synthesizing a prostacyclin analog</title><source>esp@cenet</source><creator>Chambournier, Gilles ; Hering, Kirk William ; Endres, Gregory William ; Fedij, Victor ; Krell ; Mahmoud, Hussein Mahmoud</creator><creatorcontrib>Chambournier, Gilles ; Hering, Kirk William ; Endres, Gregory William ; Fedij, Victor ; Krell ; Mahmoud, Hussein Mahmoud</creatorcontrib><description>The present invention provides processes for preparing a prostacyclin analogue of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R10 is a linear or branched C1-6 alkyl. The processes of the present invention comprise steps that generate improved yields and fewer byproducts than traditional methods. The processes of the present invention employ reagents (e.g., the oxidizing reagent) that are less toxic that those used in the traditional methods (e.g., oxalyl chloride). Many of the processes of the present invention generate intermediates with improved e.e. and chemical purity; thereby eliminating the need of additional chromatography steps. And, the processes of the present invention are scalable to generate commercial quantities of the final compound.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2020</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20200131&amp;DB=EPODOC&amp;CC=NZ&amp;NR=708130A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25562,76317</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20200131&amp;DB=EPODOC&amp;CC=NZ&amp;NR=708130A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Chambournier, Gilles</creatorcontrib><creatorcontrib>Hering, Kirk William</creatorcontrib><creatorcontrib>Endres, Gregory William</creatorcontrib><creatorcontrib>Fedij, Victor</creatorcontrib><creatorcontrib>Krell</creatorcontrib><creatorcontrib>Mahmoud, Hussein Mahmoud</creatorcontrib><title>Methods of synthesizing a prostacyclin analog</title><description>The present invention provides processes for preparing a prostacyclin analogue of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R10 is a linear or branched C1-6 alkyl. The processes of the present invention comprise steps that generate improved yields and fewer byproducts than traditional methods. The processes of the present invention employ reagents (e.g., the oxidizing reagent) that are less toxic that those used in the traditional methods (e.g., oxalyl chloride). Many of the processes of the present invention generate intermediates with improved e.e. and chemical purity; thereby eliminating the need of additional chromatography steps. And, the processes of the present invention are scalable to generate commercial quantities of the final compound.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</subject><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2020</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZND1TS3JyE8pVshPUyiuzCvJSC3OrMrMS1dIVCgoyi8uSUyuTM7JzFNIzEvMyU_nYWBNS8wpTuWF0twMcm6uIc4euqkF-fGpxQWJyal5qSXxflHmBhaGxgaOxgQVAAD6UClo</recordid><startdate>20200131</startdate><enddate>20200131</enddate><creator>Chambournier, Gilles</creator><creator>Hering, Kirk William</creator><creator>Endres, Gregory William</creator><creator>Fedij, Victor</creator><creator>Krell</creator><creator>Mahmoud, Hussein Mahmoud</creator><scope>EVB</scope></search><sort><creationdate>20200131</creationdate><title>Methods of synthesizing a prostacyclin analog</title><author>Chambournier, Gilles ; Hering, Kirk William ; Endres, Gregory William ; Fedij, Victor ; Krell ; Mahmoud, Hussein Mahmoud</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_NZ708130A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2020</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</topic><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>Chambournier, Gilles</creatorcontrib><creatorcontrib>Hering, Kirk William</creatorcontrib><creatorcontrib>Endres, Gregory William</creatorcontrib><creatorcontrib>Fedij, Victor</creatorcontrib><creatorcontrib>Krell</creatorcontrib><creatorcontrib>Mahmoud, Hussein Mahmoud</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Chambournier, Gilles</au><au>Hering, Kirk William</au><au>Endres, Gregory William</au><au>Fedij, Victor</au><au>Krell</au><au>Mahmoud, Hussein Mahmoud</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Methods of synthesizing a prostacyclin analog</title><date>2020-01-31</date><risdate>2020</risdate><abstract>The present invention provides processes for preparing a prostacyclin analogue of Formula (I) or a pharmaceutically acceptable salt thereof, wherein R10 is a linear or branched C1-6 alkyl. The processes of the present invention comprise steps that generate improved yields and fewer byproducts than traditional methods. The processes of the present invention employ reagents (e.g., the oxidizing reagent) that are less toxic that those used in the traditional methods (e.g., oxalyl chloride). Many of the processes of the present invention generate intermediates with improved e.e. and chemical purity; thereby eliminating the need of additional chromatography steps. And, the processes of the present invention are scalable to generate commercial quantities of the final compound.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_NZ708130A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title Methods of synthesizing a prostacyclin analog
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T18%3A24%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=Chambournier,%20Gilles&rft.date=2020-01-31&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ENZ708130A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true