SUBSTITUTED PHENOTHIAZINE DERIVATIVES

The substituted (10H-phenothiazin-10-yl)propyl-1-piperazines of the formula I wherein R1 is hydrogen, halogen, alkyl, alkylthio, alkoxy, trihalomethyl or the group -SO2NR2R3, X is oxygen or sulfur, m is an integer from 2 to 6, n and s are, independently, the integer zero or 1, A is alkylene and, whe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: DAVIDSON, ARNOLD B, KIERSTEAD, RICHARD W, ZIERING, ALBERT, GUTHRIE, ROBERT W
Format: Patent
Sprache:eng ; fre
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 DAVIDSON, ARNOLD B
KIERSTEAD, RICHARD W
ZIERING, ALBERT
GUTHRIE, ROBERT W
description The substituted (10H-phenothiazin-10-yl)propyl-1-piperazines of the formula I wherein R1 is hydrogen, halogen, alkyl, alkylthio, alkoxy, trihalomethyl or the group -SO2NR2R3, X is oxygen or sulfur, m is an integer from 2 to 6, n and s are, independently, the integer zero or 1, A is alkylene and, when X is oxygen, also 2-hydroxytri-methylene, and R2 and R3, independently, are hydrogen or alkyl or taken together with the nitrogen atom a 5-, 6- or 7-membered unsubstituted or substituted heterocyclic ring, the enantiomers of those compounds wherein A is 2-hydroxy-trimethylene, and the pharmaceutically acceptable acid addition salts thereof exhibit neuroleptic activity of long duration, and thus, can be used as long acting antipsychotics, particularly in the treatment of schizophrenia. They can be prepared by reacting a 1-¢3-(10H-phenothiazin-10-yl)-propyl!-4-haloalkylpiperazine with a corresponding substituted phenol.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CA1209139A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CA1209139A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CA1209139A3</originalsourceid><addsrcrecordid>eNrjZFANDnUKDvEMCQ1xdVEI8HD18w_x8HSM8vRzVXBxDfIMcwzxDHMN5mFgTUvMKU7lhdLcDPJuriHOHrqpBfnxqcUFicmpeakl8c6OhkYGlobGlo7GhFUAAE1XItw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>SUBSTITUTED PHENOTHIAZINE DERIVATIVES</title><source>esp@cenet</source><creator>DAVIDSON, ARNOLD B ; KIERSTEAD, RICHARD W ; ZIERING, ALBERT ; GUTHRIE, ROBERT W</creator><creatorcontrib>DAVIDSON, ARNOLD B ; KIERSTEAD, RICHARD W ; ZIERING, ALBERT ; GUTHRIE, ROBERT W</creatorcontrib><description>The substituted (10H-phenothiazin-10-yl)propyl-1-piperazines of the formula I wherein R1 is hydrogen, halogen, alkyl, alkylthio, alkoxy, trihalomethyl or the group -SO2NR2R3, X is oxygen or sulfur, m is an integer from 2 to 6, n and s are, independently, the integer zero or 1, A is alkylene and, when X is oxygen, also 2-hydroxytri-methylene, and R2 and R3, independently, are hydrogen or alkyl or taken together with the nitrogen atom a 5-, 6- or 7-membered unsubstituted or substituted heterocyclic ring, the enantiomers of those compounds wherein A is 2-hydroxy-trimethylene, and the pharmaceutically acceptable acid addition salts thereof exhibit neuroleptic activity of long duration, and thus, can be used as long acting antipsychotics, particularly in the treatment of schizophrenia. They can be prepared by reacting a 1-¢3-(10H-phenothiazin-10-yl)-propyl!-4-haloalkylpiperazine with a corresponding substituted phenol.</description><edition>4</edition><language>eng ; fre</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>1986</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=19860805&amp;DB=EPODOC&amp;CC=CA&amp;NR=1209139A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19860805&amp;DB=EPODOC&amp;CC=CA&amp;NR=1209139A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>DAVIDSON, ARNOLD B</creatorcontrib><creatorcontrib>KIERSTEAD, RICHARD W</creatorcontrib><creatorcontrib>ZIERING, ALBERT</creatorcontrib><creatorcontrib>GUTHRIE, ROBERT W</creatorcontrib><title>SUBSTITUTED PHENOTHIAZINE DERIVATIVES</title><description>The substituted (10H-phenothiazin-10-yl)propyl-1-piperazines of the formula I wherein R1 is hydrogen, halogen, alkyl, alkylthio, alkoxy, trihalomethyl or the group -SO2NR2R3, X is oxygen or sulfur, m is an integer from 2 to 6, n and s are, independently, the integer zero or 1, A is alkylene and, when X is oxygen, also 2-hydroxytri-methylene, and R2 and R3, independently, are hydrogen or alkyl or taken together with the nitrogen atom a 5-, 6- or 7-membered unsubstituted or substituted heterocyclic ring, the enantiomers of those compounds wherein A is 2-hydroxy-trimethylene, and the pharmaceutically acceptable acid addition salts thereof exhibit neuroleptic activity of long duration, and thus, can be used as long acting antipsychotics, particularly in the treatment of schizophrenia. They can be prepared by reacting a 1-¢3-(10H-phenothiazin-10-yl)-propyl!-4-haloalkylpiperazine with a corresponding substituted phenol.</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>1986</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFANDnUKDvEMCQ1xdVEI8HD18w_x8HSM8vRzVXBxDfIMcwzxDHMN5mFgTUvMKU7lhdLcDPJuriHOHrqpBfnxqcUFicmpeakl8c6OhkYGlobGlo7GhFUAAE1XItw</recordid><startdate>19860805</startdate><enddate>19860805</enddate><creator>DAVIDSON, ARNOLD B</creator><creator>KIERSTEAD, RICHARD W</creator><creator>ZIERING, ALBERT</creator><creator>GUTHRIE, ROBERT W</creator><scope>EVB</scope></search><sort><creationdate>19860805</creationdate><title>SUBSTITUTED PHENOTHIAZINE DERIVATIVES</title><author>DAVIDSON, ARNOLD B ; KIERSTEAD, RICHARD W ; ZIERING, ALBERT ; GUTHRIE, ROBERT W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CA1209139A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>1986</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>DAVIDSON, ARNOLD B</creatorcontrib><creatorcontrib>KIERSTEAD, RICHARD W</creatorcontrib><creatorcontrib>ZIERING, ALBERT</creatorcontrib><creatorcontrib>GUTHRIE, ROBERT W</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>DAVIDSON, ARNOLD B</au><au>KIERSTEAD, RICHARD W</au><au>ZIERING, ALBERT</au><au>GUTHRIE, ROBERT W</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SUBSTITUTED PHENOTHIAZINE DERIVATIVES</title><date>1986-08-05</date><risdate>1986</risdate><abstract>The substituted (10H-phenothiazin-10-yl)propyl-1-piperazines of the formula I wherein R1 is hydrogen, halogen, alkyl, alkylthio, alkoxy, trihalomethyl or the group -SO2NR2R3, X is oxygen or sulfur, m is an integer from 2 to 6, n and s are, independently, the integer zero or 1, A is alkylene and, when X is oxygen, also 2-hydroxytri-methylene, and R2 and R3, independently, are hydrogen or alkyl or taken together with the nitrogen atom a 5-, 6- or 7-membered unsubstituted or substituted heterocyclic ring, the enantiomers of those compounds wherein A is 2-hydroxy-trimethylene, and the pharmaceutically acceptable acid addition salts thereof exhibit neuroleptic activity of long duration, and thus, can be used as long acting antipsychotics, particularly in the treatment of schizophrenia. They can be prepared by reacting a 1-¢3-(10H-phenothiazin-10-yl)-propyl!-4-haloalkylpiperazine with a corresponding substituted phenol.</abstract><edition>4</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng ; fre
recordid cdi_epo_espacenet_CA1209139A
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 SUBSTITUTED PHENOTHIAZINE DERIVATIVES
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T07%3A25%3A31IST&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=DAVIDSON,%20ARNOLD%20B&rft.date=1986-08-05&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECA1209139A%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