Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes
The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes, 3-aminochromanes, and 3-aminothiochromanes, including their corresponding sulfoxides and sulfones, which ring-substituted compounds exhibit agonist activity at the serotonin 1A receptor, of the formula in w...
Gespeichert in:
Hauptverfasser: | , , , , |
---|---|
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 | SCHAUS, JOHN MEHNERT HOECHSTETTER, CRAIG STEVEN HUSER, DIANE LYNN PAGET JR, CHARLES JOHNSON TITUS, ROBERT DANIEL |
description | The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes, 3-aminochromanes, and 3-aminothiochromanes, including their corresponding sulfoxides and sulfones, which ring-substituted compounds exhibit agonist activity at the serotonin 1A receptor, of the formula in which R is C1-C4 alkyl, C3-C4 alkenyl, or cyclopropylmethyl; R3 is hydrogen; or R and R3 taken together are a divalent group of the formula -CH2CH2CH2-; R1 is hydrogen, C1-C4 alkyl, C3-C4 alkenyl, cyclopropylmethyl, aryl(C1-C4-alkyl), -COR4, -(CH2)nS(C1-C4 alkyl) or -(CH2)nCONR5R6; n is an integer from 1 to 4; R4 is hydrogen, C1-C4 alkyl, C1-C4 alkoxy, or phenyl; R5 and R6 are independently hydrogen, C1-C4 alkyl, or C3-C7 cycloalkyl with the proviso that when one of R5 or R6 is cycloalkyl the other is hydrogen; X is -CH2-, -O-, -S-, A is R2 is C1-C8 alkyl, substituted C1-C8 alkyl, C2-C4 alkenyl, aryl, substituted aryl, aryl(C1-C4-alkyl), substituted aryl(C1-C4 alkyl), C3-C7 cycloalkyl-substituted methyl, or C3-C7 cycloalkyl; and pharmaceutically acceptable acid addition salts thereof. |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_GR3023409TT3</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>GR3023409TT3</sourcerecordid><originalsourceid>FETCH-epo_espacenet_GR3023409TT33</originalsourceid><addsrcrecordid>eNqNjL0OwiAURlkcjPoOuENSoUtn48_csDdXuApJCwRuB9_eJmpcnb7kfCdnzWwf4kPW-VYp0EzouJIwhZjkQSihRSsJqYD0T1dShOzJw4gRq-D6LVpf0gQL4RDdF5IPv2PLVncYK-4-u2H788kcrxJzGrBmsEuQhkuvG6XbpjNG63-cF914Pbk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes</title><source>esp@cenet</source><creator>SCHAUS, JOHN MEHNERT ; HOECHSTETTER, CRAIG STEVEN ; HUSER, DIANE LYNN ; PAGET JR, CHARLES JOHNSON ; TITUS, ROBERT DANIEL</creator><creatorcontrib>SCHAUS, JOHN MEHNERT ; HOECHSTETTER, CRAIG STEVEN ; HUSER, DIANE LYNN ; PAGET JR, CHARLES JOHNSON ; TITUS, ROBERT DANIEL</creatorcontrib><description>The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes, 3-aminochromanes, and 3-aminothiochromanes, including their corresponding sulfoxides and sulfones, which ring-substituted compounds exhibit agonist activity at the serotonin 1A receptor, of the formula in which R is C1-C4 alkyl, C3-C4 alkenyl, or cyclopropylmethyl; R3 is hydrogen; or R and R3 taken together are a divalent group of the formula -CH2CH2CH2-; R1 is hydrogen, C1-C4 alkyl, C3-C4 alkenyl, cyclopropylmethyl, aryl(C1-C4-alkyl), -COR4, -(CH2)nS(C1-C4 alkyl) or -(CH2)nCONR5R6; n is an integer from 1 to 4; R4 is hydrogen, C1-C4 alkyl, C1-C4 alkoxy, or phenyl; R5 and R6 are independently hydrogen, C1-C4 alkyl, or C3-C7 cycloalkyl with the proviso that when one of R5 or R6 is cycloalkyl the other is hydrogen; X is -CH2-, -O-, -S-, A is R2 is C1-C8 alkyl, substituted C1-C8 alkyl, C2-C4 alkenyl, aryl, substituted aryl, aryl(C1-C4-alkyl), substituted aryl(C1-C4 alkyl), C3-C7 cycloalkyl-substituted methyl, or C3-C7 cycloalkyl; and pharmaceutically acceptable acid addition salts thereof.</description><edition>6</edition><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>1997</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=19970829&DB=EPODOC&CC=GR&NR=3023409T3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19970829&DB=EPODOC&CC=GR&NR=3023409T3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SCHAUS, JOHN MEHNERT</creatorcontrib><creatorcontrib>HOECHSTETTER, CRAIG STEVEN</creatorcontrib><creatorcontrib>HUSER, DIANE LYNN</creatorcontrib><creatorcontrib>PAGET JR, CHARLES JOHNSON</creatorcontrib><creatorcontrib>TITUS, ROBERT DANIEL</creatorcontrib><title>Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes</title><description>The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes, 3-aminochromanes, and 3-aminothiochromanes, including their corresponding sulfoxides and sulfones, which ring-substituted compounds exhibit agonist activity at the serotonin 1A receptor, of the formula in which R is C1-C4 alkyl, C3-C4 alkenyl, or cyclopropylmethyl; R3 is hydrogen; or R and R3 taken together are a divalent group of the formula -CH2CH2CH2-; R1 is hydrogen, C1-C4 alkyl, C3-C4 alkenyl, cyclopropylmethyl, aryl(C1-C4-alkyl), -COR4, -(CH2)nS(C1-C4 alkyl) or -(CH2)nCONR5R6; n is an integer from 1 to 4; R4 is hydrogen, C1-C4 alkyl, C1-C4 alkoxy, or phenyl; R5 and R6 are independently hydrogen, C1-C4 alkyl, or C3-C7 cycloalkyl with the proviso that when one of R5 or R6 is cycloalkyl the other is hydrogen; X is -CH2-, -O-, -S-, A is R2 is C1-C8 alkyl, substituted C1-C8 alkyl, C2-C4 alkenyl, aryl, substituted aryl, aryl(C1-C4-alkyl), substituted aryl(C1-C4 alkyl), C3-C7 cycloalkyl-substituted methyl, or C3-C7 cycloalkyl; and pharmaceutically acceptable acid addition salts thereof.</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>1997</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNjL0OwiAURlkcjPoOuENSoUtn48_csDdXuApJCwRuB9_eJmpcnb7kfCdnzWwf4kPW-VYp0EzouJIwhZjkQSihRSsJqYD0T1dShOzJw4gRq-D6LVpf0gQL4RDdF5IPv2PLVncYK-4-u2H788kcrxJzGrBmsEuQhkuvG6XbpjNG63-cF914Pbk</recordid><startdate>19970829</startdate><enddate>19970829</enddate><creator>SCHAUS, JOHN MEHNERT</creator><creator>HOECHSTETTER, CRAIG STEVEN</creator><creator>HUSER, DIANE LYNN</creator><creator>PAGET JR, CHARLES JOHNSON</creator><creator>TITUS, ROBERT DANIEL</creator><scope>EVB</scope></search><sort><creationdate>19970829</creationdate><title>Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes</title><author>SCHAUS, JOHN MEHNERT ; HOECHSTETTER, CRAIG STEVEN ; HUSER, DIANE LYNN ; PAGET JR, CHARLES JOHNSON ; TITUS, ROBERT DANIEL</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GR3023409TT33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1997</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>SCHAUS, JOHN MEHNERT</creatorcontrib><creatorcontrib>HOECHSTETTER, CRAIG STEVEN</creatorcontrib><creatorcontrib>HUSER, DIANE LYNN</creatorcontrib><creatorcontrib>PAGET JR, CHARLES JOHNSON</creatorcontrib><creatorcontrib>TITUS, ROBERT DANIEL</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SCHAUS, JOHN MEHNERT</au><au>HOECHSTETTER, CRAIG STEVEN</au><au>HUSER, DIANE LYNN</au><au>PAGET JR, CHARLES JOHNSON</au><au>TITUS, ROBERT DANIEL</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes</title><date>1997-08-29</date><risdate>1997</risdate><abstract>The present invention provides novel ring-substituted 2-amino-1,2,3,4-tetrahydronaphthalenes, 3-aminochromanes, and 3-aminothiochromanes, including their corresponding sulfoxides and sulfones, which ring-substituted compounds exhibit agonist activity at the serotonin 1A receptor, of the formula in which R is C1-C4 alkyl, C3-C4 alkenyl, or cyclopropylmethyl; R3 is hydrogen; or R and R3 taken together are a divalent group of the formula -CH2CH2CH2-; R1 is hydrogen, C1-C4 alkyl, C3-C4 alkenyl, cyclopropylmethyl, aryl(C1-C4-alkyl), -COR4, -(CH2)nS(C1-C4 alkyl) or -(CH2)nCONR5R6; n is an integer from 1 to 4; R4 is hydrogen, C1-C4 alkyl, C1-C4 alkoxy, or phenyl; R5 and R6 are independently hydrogen, C1-C4 alkyl, or C3-C7 cycloalkyl with the proviso that when one of R5 or R6 is cycloalkyl the other is hydrogen; X is -CH2-, -O-, -S-, A is R2 is C1-C8 alkyl, substituted C1-C8 alkyl, C2-C4 alkenyl, aryl, substituted aryl, aryl(C1-C4-alkyl), substituted aryl(C1-C4 alkyl), C3-C7 cycloalkyl-substituted methyl, or C3-C7 cycloalkyl; and pharmaceutically acceptable acid addition salts thereof.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | eng |
recordid | cdi_epo_espacenet_GR3023409TT3 |
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 | Ring-substituted 2-amino-1,2,3,4-tetra-hydronaphthalenes, 3-aminochromanes and 3-aminothiochromanes |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T22%3A43%3A43IST&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=SCHAUS,%20JOHN%20MEHNERT&rft.date=1997-08-29&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EGR3023409TT3%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 |