Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide

1,243,838. Analgesics. AMERICAN CYANAMID CO. 8 Nov., 1968 [12 Jan., 1968], No. 53147/68. Heading A5B. [Also in Division C2] Analgesic compositions in the form of injectable solutions or unit dosages for oral administration, comprise compounds of formula their non-toxic acid addition salts and their...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: JOHNSTON BROWN,JOHN, ALLIS HARDY,ROBERT
Format: Patent
Sprache:ger
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 JOHNSTON BROWN,JOHN
ALLIS HARDY,ROBERT
description 1,243,838. Analgesics. AMERICAN CYANAMID CO. 8 Nov., 1968 [12 Jan., 1968], No. 53147/68. Heading A5B. [Also in Division C2] Analgesic compositions in the form of injectable solutions or unit dosages for oral administration, comprise compounds of formula their non-toxic acid addition salts and their alkali metal salts (when R 1 =H) wherein R 1 is H or C 1-4 alkyl or C 2-5 alkanoyl, R 2 is H, CN, propargyl, C 1-4 alkyl (possibly Ph-substituted), C 2-6 alkenyl or cycloalkylmethyl (C 4-7 ), R 3 is H or Me, Y is -CH:CH- or -CH 2 CH 2 -, Q is a group of formula where R 4 is H or C 1-7 alkyl, is -NR 5 N=, -ON= or -N=C(NH 2 )N=, and R 5 is H, C 1-4 alkyl, Ph (possibly halo, CF 3 or C 1-4 alkyl or alkoxy substituted), pyridyl, quinolyl, benzothiazolyl, dimethylpyrimidyl or dimethyl-s-triazinyl. These compounds may be adminstered in combination with salicylates such as aspirin.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CH511232A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CH511232A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CH511232A3</originalsourceid><addsrcrecordid>eNqFy00KglAYhWEnDaLaQtxhgd9AK20aUriAaCrmPXYFvZ_cH8hW0ELaSRvLoHmjlwfOmQbPC0xdKgMtHt6IHMY6tK3XN6HhYYT1V-sa5xsYNzKlHGO5GqqWKQ33JBs1SMOUUAen-D5QEkZbgpZMq_fLKWgWLMfvF6XmNVUsGwnhtRTUsenVqHkwqcvWYvHrLFiejucsJ_RcwPZlBQ1XZPkuiuJNfNj8HXwACe5Ktg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide</title><source>esp@cenet</source><creator>JOHNSTON BROWN,JOHN ; ALLIS HARDY,ROBERT</creator><creatorcontrib>JOHNSTON BROWN,JOHN ; ALLIS HARDY,ROBERT</creatorcontrib><description>1,243,838. Analgesics. AMERICAN CYANAMID CO. 8 Nov., 1968 [12 Jan., 1968], No. 53147/68. Heading A5B. [Also in Division C2] Analgesic compositions in the form of injectable solutions or unit dosages for oral administration, comprise compounds of formula their non-toxic acid addition salts and their alkali metal salts (when R 1 =H) wherein R 1 is H or C 1-4 alkyl or C 2-5 alkanoyl, R 2 is H, CN, propargyl, C 1-4 alkyl (possibly Ph-substituted), C 2-6 alkenyl or cycloalkylmethyl (C 4-7 ), R 3 is H or Me, Y is -CH:CH- or -CH 2 CH 2 -, Q is a group of formula where R 4 is H or C 1-7 alkyl, is -NR 5 N=, -ON= or -N=C(NH 2 )N=, and R 5 is H, C 1-4 alkyl, Ph (possibly halo, CF 3 or C 1-4 alkyl or alkoxy substituted), pyridyl, quinolyl, benzothiazolyl, dimethylpyrimidyl or dimethyl-s-triazinyl. These compounds may be adminstered in combination with salicylates such as aspirin.</description><edition>1</edition><language>ger</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1971</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=19710815&amp;DB=EPODOC&amp;CC=CH&amp;NR=511232A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19710815&amp;DB=EPODOC&amp;CC=CH&amp;NR=511232A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JOHNSTON BROWN,JOHN</creatorcontrib><creatorcontrib>ALLIS HARDY,ROBERT</creatorcontrib><title>Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide</title><description>1,243,838. Analgesics. AMERICAN CYANAMID CO. 8 Nov., 1968 [12 Jan., 1968], No. 53147/68. Heading A5B. [Also in Division C2] Analgesic compositions in the form of injectable solutions or unit dosages for oral administration, comprise compounds of formula their non-toxic acid addition salts and their alkali metal salts (when R 1 =H) wherein R 1 is H or C 1-4 alkyl or C 2-5 alkanoyl, R 2 is H, CN, propargyl, C 1-4 alkyl (possibly Ph-substituted), C 2-6 alkenyl or cycloalkylmethyl (C 4-7 ), R 3 is H or Me, Y is -CH:CH- or -CH 2 CH 2 -, Q is a group of formula where R 4 is H or C 1-7 alkyl, is -NR 5 N=, -ON= or -N=C(NH 2 )N=, and R 5 is H, C 1-4 alkyl, Ph (possibly halo, CF 3 or C 1-4 alkyl or alkoxy substituted), pyridyl, quinolyl, benzothiazolyl, dimethylpyrimidyl or dimethyl-s-triazinyl. These compounds may be adminstered in combination with salicylates such as aspirin.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1971</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFy00KglAYhWEnDaLaQtxhgd9AK20aUriAaCrmPXYFvZ_cH8hW0ELaSRvLoHmjlwfOmQbPC0xdKgMtHt6IHMY6tK3XN6HhYYT1V-sa5xsYNzKlHGO5GqqWKQ33JBs1SMOUUAen-D5QEkZbgpZMq_fLKWgWLMfvF6XmNVUsGwnhtRTUsenVqHkwqcvWYvHrLFiejucsJ_RcwPZlBQ1XZPkuiuJNfNj8HXwACe5Ktg</recordid><startdate>19710815</startdate><enddate>19710815</enddate><creator>JOHNSTON BROWN,JOHN</creator><creator>ALLIS HARDY,ROBERT</creator><scope>EVB</scope></search><sort><creationdate>19710815</creationdate><title>Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide</title><author>JOHNSTON BROWN,JOHN ; ALLIS HARDY,ROBERT</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CH511232A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1971</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>JOHNSTON BROWN,JOHN</creatorcontrib><creatorcontrib>ALLIS HARDY,ROBERT</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JOHNSTON BROWN,JOHN</au><au>ALLIS HARDY,ROBERT</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide</title><date>1971-08-15</date><risdate>1971</risdate><abstract>1,243,838. Analgesics. AMERICAN CYANAMID CO. 8 Nov., 1968 [12 Jan., 1968], No. 53147/68. Heading A5B. [Also in Division C2] Analgesic compositions in the form of injectable solutions or unit dosages for oral administration, comprise compounds of formula their non-toxic acid addition salts and their alkali metal salts (when R 1 =H) wherein R 1 is H or C 1-4 alkyl or C 2-5 alkanoyl, R 2 is H, CN, propargyl, C 1-4 alkyl (possibly Ph-substituted), C 2-6 alkenyl or cycloalkylmethyl (C 4-7 ), R 3 is H or Me, Y is -CH:CH- or -CH 2 CH 2 -, Q is a group of formula where R 4 is H or C 1-7 alkyl, is -NR 5 N=, -ON= or -N=C(NH 2 )N=, and R 5 is H, C 1-4 alkyl, Ph (possibly halo, CF 3 or C 1-4 alkyl or alkoxy substituted), pyridyl, quinolyl, benzothiazolyl, dimethylpyrimidyl or dimethyl-s-triazinyl. These compounds may be adminstered in combination with salicylates such as aspirin.</abstract><edition>1</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language ger
recordid cdi_epo_espacenet_CH511232A
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title Verfahren zur Herstellung neuer substituierter 7-Heterocyclo-7,8-dihydro-6-methoxy-6,14-endo-(ätheno oder äthano)-codide und -morphide
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T10%3A59%3A39IST&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=JOHNSTON%20BROWN,JOHN&rft.date=1971-08-15&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECH511232A%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