INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME

The present invention provides intermediates useful for the synthesis of an aminopyrimidine derivative or pharmaceutically acceptable salt thereof having a selective inhibitory activity against protein kinases, especially against the protein kinases for mutant epidermal growth factor receptors; and...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: LEE DOO-BYUNG, KHOO JA-HEOUK, OH SANG-HO, LEE JUN-SUP, SHIN WOO-SEOB, LEE JUNG-AE, JU HYUN, LIM JONGUL, JEON SANG-SEOL
Format: Patent
Sprache:chi ; 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 LEE DOO-BYUNG
KHOO JA-HEOUK
OH SANG-HO
LEE JUN-SUP
SHIN WOO-SEOB
LEE JUNG-AE
JU HYUN
LIM JONGUL
JEON SANG-SEOL
description The present invention provides intermediates useful for the synthesis of an aminopyrimidine derivative or pharmaceutically acceptable salt thereof having a selective inhibitory activity against protein kinases, especially against the protein kinases for mutant epidermal growth factor receptors; and processes for preparing the same. And also, the present invention provides novel intermediates useful for said process and processes for preparing the same. 本发明提供了可用于合成对蛋白激酶,尤其是对突变表皮生长因子受体的蛋白激酶具有选择性抑制活性的氨基嘧啶衍生物或其药学上可接受的盐的中间体;及其制备方法。而且,本发明提供了可用于制备其的一种或多种所述方法的新型中间体。
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN111295381A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN111295381A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN111295381A3</originalsourceid><addsrcrecordid>eNqNjMEKgkAQQL10iOofpg_osElQx0lndUhH2VmDTiKxnaIEu_XzKfUBnR48Hm8evVk8uZJSRk8KjZJtCrCVA58T6EVGKCtUFhCUCko8nwlYcj6yHzPMkEU91K7yxAInFlQClHRSCamO2-lXO6rRsWTfM5a0jGa37j6E1Y-LaG3JJ_km9M82DH13DY_wahMxxmwPu3hvMP6n-QBcnTrZ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME</title><source>esp@cenet</source><creator>LEE DOO-BYUNG ; KHOO JA-HEOUK ; OH SANG-HO ; LEE JUN-SUP ; SHIN WOO-SEOB ; LEE JUNG-AE ; JU HYUN ; LIM JONGUL ; JEON SANG-SEOL</creator><creatorcontrib>LEE DOO-BYUNG ; KHOO JA-HEOUK ; OH SANG-HO ; LEE JUN-SUP ; SHIN WOO-SEOB ; LEE JUNG-AE ; JU HYUN ; LIM JONGUL ; JEON SANG-SEOL</creatorcontrib><description>The present invention provides intermediates useful for the synthesis of an aminopyrimidine derivative or pharmaceutically acceptable salt thereof having a selective inhibitory activity against protein kinases, especially against the protein kinases for mutant epidermal growth factor receptors; and processes for preparing the same. And also, the present invention provides novel intermediates useful for said process and processes for preparing the same. 本发明提供了可用于合成对蛋白激酶,尤其是对突变表皮生长因子受体的蛋白激酶具有选择性抑制活性的氨基嘧啶衍生物或其药学上可接受的盐的中间体;及其制备方法。而且,本发明提供了可用于制备其的一种或多种所述方法的新型中间体。</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</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=20200616&amp;DB=EPODOC&amp;CC=CN&amp;NR=111295381A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20200616&amp;DB=EPODOC&amp;CC=CN&amp;NR=111295381A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LEE DOO-BYUNG</creatorcontrib><creatorcontrib>KHOO JA-HEOUK</creatorcontrib><creatorcontrib>OH SANG-HO</creatorcontrib><creatorcontrib>LEE JUN-SUP</creatorcontrib><creatorcontrib>SHIN WOO-SEOB</creatorcontrib><creatorcontrib>LEE JUNG-AE</creatorcontrib><creatorcontrib>JU HYUN</creatorcontrib><creatorcontrib>LIM JONGUL</creatorcontrib><creatorcontrib>JEON SANG-SEOL</creatorcontrib><title>INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME</title><description>The present invention provides intermediates useful for the synthesis of an aminopyrimidine derivative or pharmaceutically acceptable salt thereof having a selective inhibitory activity against protein kinases, especially against the protein kinases for mutant epidermal growth factor receptors; and processes for preparing the same. And also, the present invention provides novel intermediates useful for said process and processes for preparing the same. 本发明提供了可用于合成对蛋白激酶,尤其是对突变表皮生长因子受体的蛋白激酶具有选择性抑制活性的氨基嘧啶衍生物或其药学上可接受的盐的中间体;及其制备方法。而且,本发明提供了可用于制备其的一种或多种所述方法的新型中间体。</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>HUMAN NECESSITIES</subject><subject>HYGIENE</subject><subject>MEDICAL OR VETERINARY SCIENCE</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><subject>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2020</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjMEKgkAQQL10iOofpg_osElQx0lndUhH2VmDTiKxnaIEu_XzKfUBnR48Hm8evVk8uZJSRk8KjZJtCrCVA58T6EVGKCtUFhCUCko8nwlYcj6yHzPMkEU91K7yxAInFlQClHRSCamO2-lXO6rRsWTfM5a0jGa37j6E1Y-LaG3JJ_km9M82DH13DY_wahMxxmwPu3hvMP6n-QBcnTrZ</recordid><startdate>20200616</startdate><enddate>20200616</enddate><creator>LEE DOO-BYUNG</creator><creator>KHOO JA-HEOUK</creator><creator>OH SANG-HO</creator><creator>LEE JUN-SUP</creator><creator>SHIN WOO-SEOB</creator><creator>LEE JUNG-AE</creator><creator>JU HYUN</creator><creator>LIM JONGUL</creator><creator>JEON SANG-SEOL</creator><scope>EVB</scope></search><sort><creationdate>20200616</creationdate><title>INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME</title><author>LEE DOO-BYUNG ; KHOO JA-HEOUK ; OH SANG-HO ; LEE JUN-SUP ; SHIN WOO-SEOB ; LEE JUNG-AE ; JU HYUN ; LIM JONGUL ; JEON SANG-SEOL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN111295381A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2020</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>HUMAN NECESSITIES</topic><topic>HYGIENE</topic><topic>MEDICAL OR VETERINARY SCIENCE</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><topic>PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</topic><toplevel>online_resources</toplevel><creatorcontrib>LEE DOO-BYUNG</creatorcontrib><creatorcontrib>KHOO JA-HEOUK</creatorcontrib><creatorcontrib>OH SANG-HO</creatorcontrib><creatorcontrib>LEE JUN-SUP</creatorcontrib><creatorcontrib>SHIN WOO-SEOB</creatorcontrib><creatorcontrib>LEE JUNG-AE</creatorcontrib><creatorcontrib>JU HYUN</creatorcontrib><creatorcontrib>LIM JONGUL</creatorcontrib><creatorcontrib>JEON SANG-SEOL</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LEE DOO-BYUNG</au><au>KHOO JA-HEOUK</au><au>OH SANG-HO</au><au>LEE JUN-SUP</au><au>SHIN WOO-SEOB</au><au>LEE JUNG-AE</au><au>JU HYUN</au><au>LIM JONGUL</au><au>JEON SANG-SEOL</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME</title><date>2020-06-16</date><risdate>2020</risdate><abstract>The present invention provides intermediates useful for the synthesis of an aminopyrimidine derivative or pharmaceutically acceptable salt thereof having a selective inhibitory activity against protein kinases, especially against the protein kinases for mutant epidermal growth factor receptors; and processes for preparing the same. And also, the present invention provides novel intermediates useful for said process and processes for preparing the same. 本发明提供了可用于合成对蛋白激酶,尤其是对突变表皮生长因子受体的蛋白激酶具有选择性抑制活性的氨基嘧啶衍生物或其药学上可接受的盐的中间体;及其制备方法。而且,本发明提供了可用于制备其的一种或多种所述方法的新型中间体。</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language chi ; eng
recordid cdi_epo_espacenet_CN111295381A
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
title INTERMEDIATES USEFUL FOR THE SYNTHESIS OF A SELECTIVE INHIBITOR AGAINST PROTEIN KINASE AND PROCESSES FOR PREPARING THE SAME
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T18%3A46%3A34IST&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=LEE%20DOO-BYUNG&rft.date=2020-06-16&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN111295381A%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