FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER

A new process is described for the production of 4-methyl-5-substituted- alkylthiomethyl-imidazoles, particularly Cimetidine of the formula by the following series of reactions wherein Alk is alkylene preferably -CH2-CH2- and Alk is C1-4 alkyl preferably CH3. The reactions for the selective reductio...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: CLAUSEN, FINN PRIESS, GELTING, NIELS, ALHEDE, BOERGE, PREIKSCHAT, HERBERT
Format: Patent
Sprache:dan
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 CLAUSEN, FINN PRIESS
GELTING, NIELS
ALHEDE, BOERGE
PREIKSCHAT, HERBERT
description A new process is described for the production of 4-methyl-5-substituted- alkylthiomethyl-imidazoles, particularly Cimetidine of the formula by the following series of reactions wherein Alk is alkylene preferably -CH2-CH2- and Alk is C1-4 alkyl preferably CH3. The reactions for the selective reduction of Y and the deoxygenation may be effected in reverse order. The starting compound may have a second oxime group replacing the keto group or the oxime and keto groups shown may be transposed. The thioether cyanoguandines produced in the first reaction step are claimed as new compounds.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DK159309BB</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DK159309BB</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DK159309BB3</originalsourceid><addsrcrecordid>eNrjZHBzC3L1dXf0cw_2dXR0cVUI8fRRAAkFAxk-nn7uCo5uCia6vq4hkT66prqOPt6RPiEenv4QAU9fTxfHKH8f1yAeBta0xJziVF4ozc0g7-Ya4uyhm1qQH59aXJCYnJqXWhLv4m1oamlsYOnkZExYBQASJyvH</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER</title><source>esp@cenet</source><creator>CLAUSEN, FINN PRIESS ; GELTING, NIELS ; ALHEDE, BOERGE ; PREIKSCHAT, HERBERT</creator><creatorcontrib>CLAUSEN, FINN PRIESS ; GELTING, NIELS ; ALHEDE, BOERGE ; PREIKSCHAT, HERBERT</creatorcontrib><description>A new process is described for the production of 4-methyl-5-substituted- alkylthiomethyl-imidazoles, particularly Cimetidine of the formula by the following series of reactions wherein Alk is alkylene preferably -CH2-CH2- and Alk is C1-4 alkyl preferably CH3. The reactions for the selective reduction of Y and the deoxygenation may be effected in reverse order. The starting compound may have a second oxime group replacing the keto group or the oxime and keto groups shown may be transposed. The thioether cyanoguandines produced in the first reaction step are claimed as new compounds.</description><edition>5</edition><language>dan</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1990</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=19901001&amp;DB=EPODOC&amp;CC=DK&amp;NR=159309B$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19901001&amp;DB=EPODOC&amp;CC=DK&amp;NR=159309B$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CLAUSEN, FINN PRIESS</creatorcontrib><creatorcontrib>GELTING, NIELS</creatorcontrib><creatorcontrib>ALHEDE, BOERGE</creatorcontrib><creatorcontrib>PREIKSCHAT, HERBERT</creatorcontrib><title>FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER</title><description>A new process is described for the production of 4-methyl-5-substituted- alkylthiomethyl-imidazoles, particularly Cimetidine of the formula by the following series of reactions wherein Alk is alkylene preferably -CH2-CH2- and Alk is C1-4 alkyl preferably CH3. The reactions for the selective reduction of Y and the deoxygenation may be effected in reverse order. The starting compound may have a second oxime group replacing the keto group or the oxime and keto groups shown may be transposed. The thioether cyanoguandines produced in the first reaction step are claimed as new compounds.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1990</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZHBzC3L1dXf0cw_2dXR0cVUI8fRRAAkFAxk-nn7uCo5uCia6vq4hkT66prqOPt6RPiEenv4QAU9fTxfHKH8f1yAeBta0xJziVF4ozc0g7-Ya4uyhm1qQH59aXJCYnJqXWhLv4m1oamlsYOnkZExYBQASJyvH</recordid><startdate>19901001</startdate><enddate>19901001</enddate><creator>CLAUSEN, FINN PRIESS</creator><creator>GELTING, NIELS</creator><creator>ALHEDE, BOERGE</creator><creator>PREIKSCHAT, HERBERT</creator><scope>EVB</scope></search><sort><creationdate>19901001</creationdate><title>FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER</title><author>CLAUSEN, FINN PRIESS ; GELTING, NIELS ; ALHEDE, BOERGE ; PREIKSCHAT, HERBERT</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DK159309BB3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>dan</language><creationdate>1990</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>CLAUSEN, FINN PRIESS</creatorcontrib><creatorcontrib>GELTING, NIELS</creatorcontrib><creatorcontrib>ALHEDE, BOERGE</creatorcontrib><creatorcontrib>PREIKSCHAT, HERBERT</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>CLAUSEN, FINN PRIESS</au><au>GELTING, NIELS</au><au>ALHEDE, BOERGE</au><au>PREIKSCHAT, HERBERT</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER</title><date>1990-10-01</date><risdate>1990</risdate><abstract>A new process is described for the production of 4-methyl-5-substituted- alkylthiomethyl-imidazoles, particularly Cimetidine of the formula by the following series of reactions wherein Alk is alkylene preferably -CH2-CH2- and Alk is C1-4 alkyl preferably CH3. The reactions for the selective reduction of Y and the deoxygenation may be effected in reverse order. The starting compound may have a second oxime group replacing the keto group or the oxime and keto groups shown may be transposed. The thioether cyanoguandines produced in the first reaction step are claimed as new compounds.</abstract><edition>5</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language dan
recordid cdi_epo_espacenet_DK159309BB
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title FREMGANGSMAADE TIL FREMSTILLING AF 4-METYL-5-ALKYLTHIOMETYL-IMIDAZOLER
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T02%3A43%3A01IST&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=CLAUSEN,%20FINN%20PRIESS&rft.date=1990-10-01&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDK159309BB%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