NOVEL BENZAZEPINE DERIVATIVE

This invention relates to benzazepine derivatives of formula I wherein A is -CH2CH2- or -CH=CH-; R1 is hydrogen, chlorine, bromine, C1-C3 alkyl, amino, C1-C3 alkylamino, C1-C3 dialkylamino, acylamino, hydroxy, C1-C3 alkoxy or phenyl C1-C3 alkoxy; R2 is hydrogen, chlorine, bromine, hydroxy, C1-C3 alk...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: KURAUSU NORU, NORUBERUTO HAUERU, KURISUCHIYAN RIRII, BARUTAA KOBINGAA, FUORUKUHARUTO AUSUTERU, MANFURETSUDO RAIFUEN, YOAHIMU HAIDAA
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 KURAUSU NORU
NORUBERUTO HAUERU
KURISUCHIYAN RIRII
BARUTAA KOBINGAA
FUORUKUHARUTO AUSUTERU
MANFURETSUDO RAIFUEN
YOAHIMU HAIDAA
description This invention relates to benzazepine derivatives of formula I wherein A is -CH2CH2- or -CH=CH-; R1 is hydrogen, chlorine, bromine, C1-C3 alkyl, amino, C1-C3 alkylamino, C1-C3 dialkylamino, acylamino, hydroxy, C1-C3 alkoxy or phenyl C1-C3 alkoxy; R2 is hydrogen, chlorine, bromine, hydroxy, C1-C3 alkyl, C1-C3 alkoxy or phenyl C1-C3 alkoxy or, together with R1, can be C1-C3 alkylenedioxy; R3 is hydrogen, chlorine, bromine or C1-C3 alkoxy; R4 is hydrogen, benzyl, C1-C3 alkyl or C3-C5 alkenyl; R5 is hydrogen, halogen, C1-C3 alkyl or C1-C3 alkoxy; R6 is hydrogen, C1-C3 alkyl or C1-C3 alkoxy or, together with R5, can be a C1-C2 alkylenedioxy; X is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is oxygen, sulphur, sulphinyl or sulphonyl; Y is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is methylene or carbonyl; m and n are each independently 2, 3 or 4; and nontoxic, pharmaceutically acceptable addition salts thereof. These compounds have valuable pharmacological properties, particularly the effect of lowering heart rate and reducing the O2 requirement of the heart.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_JPS60255770A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>JPS60255770A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_JPS60255770A3</originalsourceid><addsrcrecordid>eNrjZJDx8w9z9VFwcvWLcoxyDfD0c1VwcQ3yDHMM8Qxz5WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BwWYGRqam5uYGjsbEqAEAjIchTQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>NOVEL BENZAZEPINE DERIVATIVE</title><source>esp@cenet</source><creator>KURAUSU NORU ; NORUBERUTO HAUERU ; KURISUCHIYAN RIRII ; BARUTAA KOBINGAA ; FUORUKUHARUTO AUSUTERU ; MANFURETSUDO RAIFUEN ; YOAHIMU HAIDAA</creator><creatorcontrib>KURAUSU NORU ; NORUBERUTO HAUERU ; KURISUCHIYAN RIRII ; BARUTAA KOBINGAA ; FUORUKUHARUTO AUSUTERU ; MANFURETSUDO RAIFUEN ; YOAHIMU HAIDAA</creatorcontrib><description>This invention relates to benzazepine derivatives of formula I wherein A is -CH2CH2- or -CH=CH-; R1 is hydrogen, chlorine, bromine, C1-C3 alkyl, amino, C1-C3 alkylamino, C1-C3 dialkylamino, acylamino, hydroxy, C1-C3 alkoxy or phenyl C1-C3 alkoxy; R2 is hydrogen, chlorine, bromine, hydroxy, C1-C3 alkyl, C1-C3 alkoxy or phenyl C1-C3 alkoxy or, together with R1, can be C1-C3 alkylenedioxy; R3 is hydrogen, chlorine, bromine or C1-C3 alkoxy; R4 is hydrogen, benzyl, C1-C3 alkyl or C3-C5 alkenyl; R5 is hydrogen, halogen, C1-C3 alkyl or C1-C3 alkoxy; R6 is hydrogen, C1-C3 alkyl or C1-C3 alkoxy or, together with R5, can be a C1-C2 alkylenedioxy; X is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is oxygen, sulphur, sulphinyl or sulphonyl; Y is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is methylene or carbonyl; m and n are each independently 2, 3 or 4; and nontoxic, pharmaceutically acceptable addition salts thereof. These compounds have valuable pharmacological properties, particularly the effect of lowering heart rate and reducing the O2 requirement of the heart.</description><language>eng</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1985</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=19851217&amp;DB=EPODOC&amp;CC=JP&amp;NR=S60255770A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19851217&amp;DB=EPODOC&amp;CC=JP&amp;NR=S60255770A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KURAUSU NORU</creatorcontrib><creatorcontrib>NORUBERUTO HAUERU</creatorcontrib><creatorcontrib>KURISUCHIYAN RIRII</creatorcontrib><creatorcontrib>BARUTAA KOBINGAA</creatorcontrib><creatorcontrib>FUORUKUHARUTO AUSUTERU</creatorcontrib><creatorcontrib>MANFURETSUDO RAIFUEN</creatorcontrib><creatorcontrib>YOAHIMU HAIDAA</creatorcontrib><title>NOVEL BENZAZEPINE DERIVATIVE</title><description>This invention relates to benzazepine derivatives of formula I wherein A is -CH2CH2- or -CH=CH-; R1 is hydrogen, chlorine, bromine, C1-C3 alkyl, amino, C1-C3 alkylamino, C1-C3 dialkylamino, acylamino, hydroxy, C1-C3 alkoxy or phenyl C1-C3 alkoxy; R2 is hydrogen, chlorine, bromine, hydroxy, C1-C3 alkyl, C1-C3 alkoxy or phenyl C1-C3 alkoxy or, together with R1, can be C1-C3 alkylenedioxy; R3 is hydrogen, chlorine, bromine or C1-C3 alkoxy; R4 is hydrogen, benzyl, C1-C3 alkyl or C3-C5 alkenyl; R5 is hydrogen, halogen, C1-C3 alkyl or C1-C3 alkoxy; R6 is hydrogen, C1-C3 alkyl or C1-C3 alkoxy or, together with R5, can be a C1-C2 alkylenedioxy; X is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is oxygen, sulphur, sulphinyl or sulphonyl; Y is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is methylene or carbonyl; m and n are each independently 2, 3 or 4; and nontoxic, pharmaceutically acceptable addition salts thereof. These compounds have valuable pharmacological properties, particularly the effect of lowering heart rate and reducing the O2 requirement of the heart.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><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><subject>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1985</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJDx8w9z9VFwcvWLcoxyDfD0c1VwcQ3yDHMM8Qxz5WFgTUvMKU7lhdLcDIpuriHOHrqpBfnxqcUFicmpeakl8V4BwWYGRqam5uYGjsbEqAEAjIchTQ</recordid><startdate>19851217</startdate><enddate>19851217</enddate><creator>KURAUSU NORU</creator><creator>NORUBERUTO HAUERU</creator><creator>KURISUCHIYAN RIRII</creator><creator>BARUTAA KOBINGAA</creator><creator>FUORUKUHARUTO AUSUTERU</creator><creator>MANFURETSUDO RAIFUEN</creator><creator>YOAHIMU HAIDAA</creator><scope>EVB</scope></search><sort><creationdate>19851217</creationdate><title>NOVEL BENZAZEPINE DERIVATIVE</title><author>KURAUSU NORU ; NORUBERUTO HAUERU ; KURISUCHIYAN RIRII ; BARUTAA KOBINGAA ; FUORUKUHARUTO AUSUTERU ; MANFURETSUDO RAIFUEN ; YOAHIMU HAIDAA</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_JPS60255770A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1985</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><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><topic>SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</topic><toplevel>online_resources</toplevel><creatorcontrib>KURAUSU NORU</creatorcontrib><creatorcontrib>NORUBERUTO HAUERU</creatorcontrib><creatorcontrib>KURISUCHIYAN RIRII</creatorcontrib><creatorcontrib>BARUTAA KOBINGAA</creatorcontrib><creatorcontrib>FUORUKUHARUTO AUSUTERU</creatorcontrib><creatorcontrib>MANFURETSUDO RAIFUEN</creatorcontrib><creatorcontrib>YOAHIMU HAIDAA</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KURAUSU NORU</au><au>NORUBERUTO HAUERU</au><au>KURISUCHIYAN RIRII</au><au>BARUTAA KOBINGAA</au><au>FUORUKUHARUTO AUSUTERU</au><au>MANFURETSUDO RAIFUEN</au><au>YOAHIMU HAIDAA</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>NOVEL BENZAZEPINE DERIVATIVE</title><date>1985-12-17</date><risdate>1985</risdate><abstract>This invention relates to benzazepine derivatives of formula I wherein A is -CH2CH2- or -CH=CH-; R1 is hydrogen, chlorine, bromine, C1-C3 alkyl, amino, C1-C3 alkylamino, C1-C3 dialkylamino, acylamino, hydroxy, C1-C3 alkoxy or phenyl C1-C3 alkoxy; R2 is hydrogen, chlorine, bromine, hydroxy, C1-C3 alkyl, C1-C3 alkoxy or phenyl C1-C3 alkoxy or, together with R1, can be C1-C3 alkylenedioxy; R3 is hydrogen, chlorine, bromine or C1-C3 alkoxy; R4 is hydrogen, benzyl, C1-C3 alkyl or C3-C5 alkenyl; R5 is hydrogen, halogen, C1-C3 alkyl or C1-C3 alkoxy; R6 is hydrogen, C1-C3 alkyl or C1-C3 alkoxy or, together with R5, can be a C1-C2 alkylenedioxy; X is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is oxygen, sulphur, sulphinyl or sulphonyl; Y is an imino, optionally substituted by a benzyl or C1-C3 alkyl, or is methylene or carbonyl; m and n are each independently 2, 3 or 4; and nontoxic, pharmaceutically acceptable addition salts thereof. These compounds have valuable pharmacological properties, particularly the effect of lowering heart rate and reducing the O2 requirement of the heart.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_JPS60255770A
source esp@cenet
subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title NOVEL BENZAZEPINE DERIVATIVE
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T13%3A14%3A16IST&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=KURAUSU%20NORU&rft.date=1985-12-17&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EJPS60255770A%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