New bi:phenyl-methyl-benzimidazole derivs

1-Biphenylylmethyl-benzimidazole derivs. of formula (I) and their tautomers and salts are new: R1 = F, Cl, Br, 1-3C alkyl or CF3; R2 = opt. substd. C-bonded 5-membered heteroaryl contg. one heteroatom (NH, O or S) or two heteroatoms (NH and O, S or N), opt. fused to another ring; a pyrrolidino, pipe...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: RIES, UWE. DR., 88400 BIBERACH, DE, HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE, MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE, WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE, MIHM, GERHARD. DR., 88440 BIBERACH, DE, ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE
Format: Patent
Sprache:eng ; 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 RIES, UWE. DR., 88400 BIBERACH, DE
HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE
MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE
WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE
MIHM, GERHARD. DR., 88440 BIBERACH, DE
ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE
description 1-Biphenylylmethyl-benzimidazole derivs. of formula (I) and their tautomers and salts are new: R1 = F, Cl, Br, 1-3C alkyl or CF3; R2 = opt. substd. C-bonded 5-membered heteroaryl contg. one heteroatom (NH, O or S) or two heteroatoms (NH and O, S or N), opt. fused to another ring; a pyrrolidino, piperidino or hexamethylenimino gp. in which a CH2 gp. is replaced by CO or SO2; opt. substd. maleimido (opt. substd. by 1-3C alkyl or phenyl), or opt. substd. 2,4-dioxo-3-imidazolidinyl; R3 = 1-4C alkyl, 3-5C cycloalkyl, 1-3C alkoxy or 1-3C alkylthio; R4 = opt. substd. amino, substd. sulphonyl, C(NH)NHOH; 2,4-dioxo-5-thiazolidinylidenemethyl; or 5-oxo-1,2,4-oxadiazol-3-yl.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_DE4408497A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>DE4408497A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_DE4408497A13</originalsourceid><addsrcrecordid>eNrjZND0Sy1XSMq0KshIzavM0c1NLckAUkmpeVWZuZkpiVX5OakKKalFmWXFPAysaYk5xam8UJqbQcHNNcTZQze1ID8-tbggMTk1L7Uk3sXVxMTAwsTS3NHQmAglAMsxKI4</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>New bi:phenyl-methyl-benzimidazole derivs</title><source>esp@cenet</source><creator>RIES, UWE. DR., 88400 BIBERACH, DE ; HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE ; MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE ; WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE ; MIHM, GERHARD. DR., 88440 BIBERACH, DE ; ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</creator><creatorcontrib>RIES, UWE. DR., 88400 BIBERACH, DE ; HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE ; MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE ; WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE ; MIHM, GERHARD. DR., 88440 BIBERACH, DE ; ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</creatorcontrib><description>1-Biphenylylmethyl-benzimidazole derivs. of formula (I) and their tautomers and salts are new: R1 = F, Cl, Br, 1-3C alkyl or CF3; R2 = opt. substd. C-bonded 5-membered heteroaryl contg. one heteroatom (NH, O or S) or two heteroatoms (NH and O, S or N), opt. fused to another ring; a pyrrolidino, piperidino or hexamethylenimino gp. in which a CH2 gp. is replaced by CO or SO2; opt. substd. maleimido (opt. substd. by 1-3C alkyl or phenyl), or opt. substd. 2,4-dioxo-3-imidazolidinyl; R3 = 1-4C alkyl, 3-5C cycloalkyl, 1-3C alkoxy or 1-3C alkylthio; R4 = opt. substd. amino, substd. sulphonyl, C(NH)NHOH; 2,4-dioxo-5-thiazolidinylidenemethyl; or 5-oxo-1,2,4-oxadiazol-3-yl.</description><edition>6</edition><language>eng ; ger</language><subject>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>1995</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=19950921&amp;DB=EPODOC&amp;CC=DE&amp;NR=4408497A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19950921&amp;DB=EPODOC&amp;CC=DE&amp;NR=4408497A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>RIES, UWE. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE</creatorcontrib><creatorcontrib>MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE</creatorcontrib><creatorcontrib>WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE</creatorcontrib><creatorcontrib>MIHM, GERHARD. DR., 88440 BIBERACH, DE</creatorcontrib><creatorcontrib>ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</creatorcontrib><title>New bi:phenyl-methyl-benzimidazole derivs</title><description>1-Biphenylylmethyl-benzimidazole derivs. of formula (I) and their tautomers and salts are new: R1 = F, Cl, Br, 1-3C alkyl or CF3; R2 = opt. substd. C-bonded 5-membered heteroaryl contg. one heteroatom (NH, O or S) or two heteroatoms (NH and O, S or N), opt. fused to another ring; a pyrrolidino, piperidino or hexamethylenimino gp. in which a CH2 gp. is replaced by CO or SO2; opt. substd. maleimido (opt. substd. by 1-3C alkyl or phenyl), or opt. substd. 2,4-dioxo-3-imidazolidinyl; R3 = 1-4C alkyl, 3-5C cycloalkyl, 1-3C alkoxy or 1-3C alkylthio; R4 = opt. substd. amino, substd. sulphonyl, C(NH)NHOH; 2,4-dioxo-5-thiazolidinylidenemethyl; or 5-oxo-1,2,4-oxadiazol-3-yl.</description><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>1995</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZND0Sy1XSMq0KshIzavM0c1NLckAUkmpeVWZuZkpiVX5OakKKalFmWXFPAysaYk5xam8UJqbQcHNNcTZQze1ID8-tbggMTk1L7Uk3sXVxMTAwsTS3NHQmAglAMsxKI4</recordid><startdate>19950921</startdate><enddate>19950921</enddate><creator>RIES, UWE. DR., 88400 BIBERACH, DE</creator><creator>HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE</creator><creator>MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE</creator><creator>WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE</creator><creator>MIHM, GERHARD. DR., 88440 BIBERACH, DE</creator><creator>ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</creator><scope>EVB</scope></search><sort><creationdate>19950921</creationdate><title>New bi:phenyl-methyl-benzimidazole derivs</title><author>RIES, UWE. DR., 88400 BIBERACH, DE ; HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE ; MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE ; WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE ; MIHM, GERHARD. DR., 88440 BIBERACH, DE ; ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE4408497A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; ger</language><creationdate>1995</creationdate><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>RIES, UWE. DR., 88400 BIBERACH, DE</creatorcontrib><creatorcontrib>HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE</creatorcontrib><creatorcontrib>MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE</creatorcontrib><creatorcontrib>WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE</creatorcontrib><creatorcontrib>MIHM, GERHARD. DR., 88440 BIBERACH, DE</creatorcontrib><creatorcontrib>ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>RIES, UWE. DR., 88400 BIBERACH, DE</au><au>HAUEL, NORBERT. DR., 88433 SMERHOFEN, DE</au><au>MEEL, JACPUES VAN., 88441 MITTELBIBERACH, DE</au><au>WIENEN, WOLFGANG-BIOL. DR., 88437 AEPFINGEN, DE</au><au>MIHM, GERHARD. DR., 88440 BIBERACH, DE</au><au>ENTZEROTH, MICHAEL. DR., 88447 WARTHAUSEN, DE</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>New bi:phenyl-methyl-benzimidazole derivs</title><date>1995-09-21</date><risdate>1995</risdate><abstract>1-Biphenylylmethyl-benzimidazole derivs. of formula (I) and their tautomers and salts are new: R1 = F, Cl, Br, 1-3C alkyl or CF3; R2 = opt. substd. C-bonded 5-membered heteroaryl contg. one heteroatom (NH, O or S) or two heteroatoms (NH and O, S or N), opt. fused to another ring; a pyrrolidino, piperidino or hexamethylenimino gp. in which a CH2 gp. is replaced by CO or SO2; opt. substd. maleimido (opt. substd. by 1-3C alkyl or phenyl), or opt. substd. 2,4-dioxo-3-imidazolidinyl; R3 = 1-4C alkyl, 3-5C cycloalkyl, 1-3C alkoxy or 1-3C alkylthio; R4 = opt. substd. amino, substd. sulphonyl, C(NH)NHOH; 2,4-dioxo-5-thiazolidinylidenemethyl; or 5-oxo-1,2,4-oxadiazol-3-yl.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng ; ger
recordid cdi_epo_espacenet_DE4408497A1
source esp@cenet
subjects 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 New bi:phenyl-methyl-benzimidazole derivs
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%3A22%3A44IST&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=RIES,%20UWE.%20DR.,%2088400%20BIBERACH,%20DE&rft.date=1995-09-21&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EDE4408497A1%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