Fremgangsmåte for fremstilling av 1,4-dihydropyridiner
A process for the preparation of 1,4-dihydropyridines of general formula (I) or acid addition salts thereof, comprising the steps of reacting an acetal of general formula (II) with R ONH2 or an acid addition salt thereof, so as to provide an oxime of general formula (III) in which formulae R each, i...
Gespeichert in:
Hauptverfasser: | , , |
---|---|
Format: | Patent |
Sprache: | nor |
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 | PEDERSEN, SOEREN BOLS KARUP, GUNNAR LEO PREIKSCHAT, HERBERT FRITZ |
description | A process for the preparation of 1,4-dihydropyridines of general formula (I) or acid addition salts thereof, comprising the steps of reacting an acetal of general formula (II) with R ONH2 or an acid addition salt thereof, so as to provide an oxime of general formula (III) in which formulae R each, independently, represents H, Cl or CF3, R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, n is 1 or 2, R and R , which may be the same or different, represents C1-C5 alkyl, C3-C6 cycloalkyl, aralkyl or together represent -(CH2)m-, wherein m is 2 or 3, and R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, and reducing the formed oxime of formula (III) so as to provide a 1,4-dihydropyridine of formula (I), and, if desired, converting a compound of formula (I) obtained as the free base into a pharmaceutically acceptable acid addition salt thereof or vice versa, and novel intermediates of the formulae (II) and (III) are described. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_NO314900BB1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>NO314900BB1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_NO314900BB13</originalsourceid><addsrcrecordid>eNrjZDB3K0rNTU_MSy_OPby0JFUhLb9IIQ0oVFySmZOTmZeukFimYKhjopuSmVGZUpRfUFmUmZKZl1rEw8CalphTnMoLpbkZFNxcQ5w9dFML8uNTiwsSk1PzUkvi_fyNDU0sDQycnAyNiVACANiBLls</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Fremgangsmåte for fremstilling av 1,4-dihydropyridiner</title><source>esp@cenet</source><creator>PEDERSEN, SOEREN BOLS ; KARUP, GUNNAR LEO ; PREIKSCHAT, HERBERT FRITZ</creator><creatorcontrib>PEDERSEN, SOEREN BOLS ; KARUP, GUNNAR LEO ; PREIKSCHAT, HERBERT FRITZ</creatorcontrib><description>A process for the preparation of 1,4-dihydropyridines of general formula (I) or acid addition salts thereof, comprising the steps of reacting an acetal of general formula (II) with R ONH2 or an acid addition salt thereof, so as to provide an oxime of general formula (III) in which formulae R each, independently, represents H, Cl or CF3, R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, n is 1 or 2, R and R , which may be the same or different, represents C1-C5 alkyl, C3-C6 cycloalkyl, aralkyl or together represent -(CH2)m-, wherein m is 2 or 3, and R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, and reducing the formed oxime of formula (III) so as to provide a 1,4-dihydropyridine of formula (I), and, if desired, converting a compound of formula (I) obtained as the free base into a pharmaceutically acceptable acid addition salt thereof or vice versa, and novel intermediates of the formulae (II) and (III) are described.</description><edition>7</edition><language>nor</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2003</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&date=20030610&DB=EPODOC&CC=NO&NR=314900B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20030610&DB=EPODOC&CC=NO&NR=314900B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>PEDERSEN, SOEREN BOLS</creatorcontrib><creatorcontrib>KARUP, GUNNAR LEO</creatorcontrib><creatorcontrib>PREIKSCHAT, HERBERT FRITZ</creatorcontrib><title>Fremgangsmåte for fremstilling av 1,4-dihydropyridiner</title><description>A process for the preparation of 1,4-dihydropyridines of general formula (I) or acid addition salts thereof, comprising the steps of reacting an acetal of general formula (II) with R ONH2 or an acid addition salt thereof, so as to provide an oxime of general formula (III) in which formulae R each, independently, represents H, Cl or CF3, R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, n is 1 or 2, R and R , which may be the same or different, represents C1-C5 alkyl, C3-C6 cycloalkyl, aralkyl or together represent -(CH2)m-, wherein m is 2 or 3, and R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, and reducing the formed oxime of formula (III) so as to provide a 1,4-dihydropyridine of formula (I), and, if desired, converting a compound of formula (I) obtained as the free base into a pharmaceutically acceptable acid addition salt thereof or vice versa, and novel intermediates of the formulae (II) and (III) are described.</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>2003</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDB3K0rNTU_MSy_OPby0JFUhLb9IIQ0oVFySmZOTmZeukFimYKhjopuSmVGZUpRfUFmUmZKZl1rEw8CalphTnMoLpbkZFNxcQ5w9dFML8uNTiwsSk1PzUkvi_fyNDU0sDQycnAyNiVACANiBLls</recordid><startdate>20030610</startdate><enddate>20030610</enddate><creator>PEDERSEN, SOEREN BOLS</creator><creator>KARUP, GUNNAR LEO</creator><creator>PREIKSCHAT, HERBERT FRITZ</creator><scope>EVB</scope></search><sort><creationdate>20030610</creationdate><title>Fremgangsmåte for fremstilling av 1,4-dihydropyridiner</title><author>PEDERSEN, SOEREN BOLS ; KARUP, GUNNAR LEO ; PREIKSCHAT, HERBERT FRITZ</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_NO314900BB13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>nor</language><creationdate>2003</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>PEDERSEN, SOEREN BOLS</creatorcontrib><creatorcontrib>KARUP, GUNNAR LEO</creatorcontrib><creatorcontrib>PREIKSCHAT, HERBERT FRITZ</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>PEDERSEN, SOEREN BOLS</au><au>KARUP, GUNNAR LEO</au><au>PREIKSCHAT, HERBERT FRITZ</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Fremgangsmåte for fremstilling av 1,4-dihydropyridiner</title><date>2003-06-10</date><risdate>2003</risdate><abstract>A process for the preparation of 1,4-dihydropyridines of general formula (I) or acid addition salts thereof, comprising the steps of reacting an acetal of general formula (II) with R ONH2 or an acid addition salt thereof, so as to provide an oxime of general formula (III) in which formulae R each, independently, represents H, Cl or CF3, R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, n is 1 or 2, R and R , which may be the same or different, represents C1-C5 alkyl, C3-C6 cycloalkyl, aralkyl or together represent -(CH2)m-, wherein m is 2 or 3, and R represents H, C1-C5 alkyl, C3-C6 cycloalkyl or aralkyl, and reducing the formed oxime of formula (III) so as to provide a 1,4-dihydropyridine of formula (I), and, if desired, converting a compound of formula (I) obtained as the free base into a pharmaceutically acceptable acid addition salt thereof or vice versa, and novel intermediates of the formulae (II) and (III) are described.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | nor |
recordid | cdi_epo_espacenet_NO314900BB1 |
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 | Fremgangsmåte for fremstilling av 1,4-dihydropyridiner |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T11%3A54%3A29IST&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=PEDERSEN,%20SOEREN%20BOLS&rft.date=2003-06-10&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ENO314900BB1%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 |