SUBSTITUTED OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF

Substituted oxazolidinone compounds of formula (I) and their salts are new. A = 6-membered aromatic heterocycle (containing at least one N and which is linked via C), a 6-membered, bi- or tricyclic aromatic heterocycle (containing at least one N and which is linked via C), beta -carbolin-3-yl, indol...

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Hauptverfasser: STOLLE ANDREAS DR, RUPPELT MARTIN DR, HABICH DIETER DR, RIEDL BERND DR, ENDERMANN RAINER DR, KROLL HEIN PETER DR, GUARNIERI WALTER DR, BARTEL STEPHAN DR
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creator STOLLE ANDREAS DR
RUPPELT MARTIN DR
HABICH DIETER DR
RIEDL BERND DR
ENDERMANN RAINER DR
KROLL HEIN PETER DR
GUARNIERI WALTER DR
BARTEL STEPHAN DR
description Substituted oxazolidinone compounds of formula (I) and their salts are new. A = 6-membered aromatic heterocycle (containing at least one N and which is linked via C), a 6-membered, bi- or tricyclic aromatic heterocycle (containing at least one N and which is linked via C), beta -carbolin-3-yl, indolizinyl (linked via the 6-membered ring), or a 5-membered aromatic heterocycle (containing up to 3 N, O and/or S, which may also be fused to a benzene or naphthalene ring, and which is linked via C), all of these cyclic groups being optionally substituted by (a) 1-3 COOH, halo, CN, mercapto, CHO, pyridyl, phenyl, CF3, NO2, TO, T', TS or Ac, or (b) T or 2-6C alkenyl (themselves optionally substituted by phenyl); or a group of formula (i)-(iv): R -R = H, COOH, halo, CN, CHO, CF3, NO2, T or CONR R ; R , R = H, 1-4C alkyl or phenyl; R , R -R = H, 3-6C cycloalkylcarbonyl, 3-6C cycloalkyl, T', or 1-10C alkyl (optionally substituted by CN, CF3, halo, phenyl, OH, COOH, T', 6-10C aryl, 3-6C cycloalkyl, (CO)cNR R , R -NH-SO2-R , R R NSO2 or R S(O)d); c = 0 or 1; R -R = H, 1-4C alkyl or phenyl; or together with the nitrogen atom, these groups form a 5-6 membered saturated heterocycle which optionally contains a further N, O or S heteroatom, and which is optionally substituted on C or N by 1-3C alkyl or 1-3C acyl; R , R = H, 1-4C alkyl or phenyl; d = 0-2; R , R = 1-4C alkyl, benzyl, phenyl, tolyl, or 1-6C acyl (optionally substituted by CF3, CCl3 or OR ); R = H, T (optionally substituted by aryl containing up to 10C), or (CO)eNR R , NR -SO2R , R R NSO2 or R -S(O)f; e = 0 or 1; R -R = as R -R ; R , R = H, 1-4C alkyl or phenyl; f = 0-2; R , R = as R , R ; D = O or S(O)g; g = 0-2; E, L = O or S; G, M, T, Q = O, S or NR ; R = H or 1-5C alkyl; a, b = 1 or 2; R = C(=S)R , C(=NR )R , C(=O)-(CH2)hOR , CN, a group Q or C(R )=C(R )NO2: R = 1-7C alkyl, 3-6C cycloalkyl, phenyl or NR R ; R , R = H, 1-4C alkyl or phenyl; R = H, CN, 3-6C cycloalkyl, phenyl or 1-7C alkyl; R = H, 1-7C alkyl, phenyl, 3-6C cycloalkyl, or NR R ; R , R = H, 1-4C alkyl or phenyl; h = 1-4; R = T or benzyl; R , R = H or T; Q = a 5-7 membered, saturated, partially unsaturated, or unsaturated heterocycle, containing up to 3 heteroatoms (selected from N, O and/or S) and which is optionally substituted on C or N by benzyl, halo or 1-5C alkyl; T =1-6C alkyl; T' = 1-6C alkoxycarbonyl; and Ac = 1-6C acyl.
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fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CZ34097A3</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CZ34097A3</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CZ34097A33</originalsourceid><addsrcrecordid>eNqFi8EKgkAURd20iOoXYj7AIDCIlq_xmQ903jDzBsSNSEyrKMH6_xTct7qHw7nr5OvD1QtJEMwVN9ByRTkZNuhTZR1r9F5xoaREcpNACw6E2KSLCh4VmFzZElwNGoOQhkppri17msuJjQAZMrf545CLbbJ69M8x7pbdJPsCRZeHOLy7OA79Pb7ip9NtdjpezpBlf4MfCYI4rw</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>SUBSTITUTED OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF</title><source>esp@cenet</source><creator>STOLLE ANDREAS DR ; RUPPELT MARTIN DR ; HABICH DIETER DR ; RIEDL BERND DR ; ENDERMANN RAINER DR ; KROLL HEIN PETER DR ; GUARNIERI WALTER DR ; BARTEL STEPHAN DR</creator><creatorcontrib>STOLLE ANDREAS DR ; RUPPELT MARTIN DR ; HABICH DIETER DR ; RIEDL BERND DR ; ENDERMANN RAINER DR ; KROLL HEIN PETER DR ; GUARNIERI WALTER DR ; BARTEL STEPHAN DR</creatorcontrib><description>Substituted oxazolidinone compounds of formula (I) and their salts are new. A = 6-membered aromatic heterocycle (containing at least one N and which is linked via C), a 6-membered, bi- or tricyclic aromatic heterocycle (containing at least one N and which is linked via C), beta -carbolin-3-yl, indolizinyl (linked via the 6-membered ring), or a 5-membered aromatic heterocycle (containing up to 3 N, O and/or S, which may also be fused to a benzene or naphthalene ring, and which is linked via C), all of these cyclic groups being optionally substituted by (a) 1-3 COOH, halo, CN, mercapto, CHO, pyridyl, phenyl, CF3, NO2, TO, T', TS or Ac, or (b) T or 2-6C alkenyl (themselves optionally substituted by phenyl); or a group of formula (i)-(iv): R -R = H, COOH, halo, CN, CHO, CF3, NO2, T or CONR R ; R , R = H, 1-4C alkyl or phenyl; R , R -R = H, 3-6C cycloalkylcarbonyl, 3-6C cycloalkyl, T', or 1-10C alkyl (optionally substituted by CN, CF3, halo, phenyl, OH, COOH, T', 6-10C aryl, 3-6C cycloalkyl, (CO)cNR R , R -NH-SO2-R , R R NSO2 or R S(O)d); c = 0 or 1; R -R = H, 1-4C alkyl or phenyl; or together with the nitrogen atom, these groups form a 5-6 membered saturated heterocycle which optionally contains a further N, O or S heteroatom, and which is optionally substituted on C or N by 1-3C alkyl or 1-3C acyl; R , R = H, 1-4C alkyl or phenyl; d = 0-2; R , R = 1-4C alkyl, benzyl, phenyl, tolyl, or 1-6C acyl (optionally substituted by CF3, CCl3 or OR ); R = H, T (optionally substituted by aryl containing up to 10C), or (CO)eNR R , NR -SO2R , R R NSO2 or R -S(O)f; e = 0 or 1; R -R = as R -R ; R , R = H, 1-4C alkyl or phenyl; f = 0-2; R , R = as R , R ; D = O or S(O)g; g = 0-2; E, L = O or S; G, M, T, Q = O, S or NR ; R = H or 1-5C alkyl; a, b = 1 or 2; R = C(=S)R , C(=NR )R , C(=O)-(CH2)hOR , CN, a group Q or C(R )=C(R )NO2: R = 1-7C alkyl, 3-6C cycloalkyl, phenyl or NR R ; R , R = H, 1-4C alkyl or phenyl; R = H, CN, 3-6C cycloalkyl, phenyl or 1-7C alkyl; R = H, 1-7C alkyl, phenyl, 3-6C cycloalkyl, or NR R ; R , R = H, 1-4C alkyl or phenyl; h = 1-4; R = T or benzyl; R , R = H or T; Q = a 5-7 membered, saturated, partially unsaturated, or unsaturated heterocycle, containing up to 3 heteroatoms (selected from N, O and/or S) and which is optionally substituted on C or N by benzyl, halo or 1-5C alkyl; T =1-6C alkyl; T' = 1-6C alkoxycarbonyl; and Ac = 1-6C acyl.</description><edition>6</edition><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; 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&amp;date=19970813&amp;DB=EPODOC&amp;CC=CZ&amp;NR=34097A3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19970813&amp;DB=EPODOC&amp;CC=CZ&amp;NR=34097A3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>STOLLE ANDREAS DR</creatorcontrib><creatorcontrib>RUPPELT MARTIN DR</creatorcontrib><creatorcontrib>HABICH DIETER DR</creatorcontrib><creatorcontrib>RIEDL BERND DR</creatorcontrib><creatorcontrib>ENDERMANN RAINER DR</creatorcontrib><creatorcontrib>KROLL HEIN PETER DR</creatorcontrib><creatorcontrib>GUARNIERI WALTER DR</creatorcontrib><creatorcontrib>BARTEL STEPHAN DR</creatorcontrib><title>SUBSTITUTED OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF</title><description>Substituted oxazolidinone compounds of formula (I) and their salts are new. A = 6-membered aromatic heterocycle (containing at least one N and which is linked via C), a 6-membered, bi- or tricyclic aromatic heterocycle (containing at least one N and which is linked via C), beta -carbolin-3-yl, indolizinyl (linked via the 6-membered ring), or a 5-membered aromatic heterocycle (containing up to 3 N, O and/or S, which may also be fused to a benzene or naphthalene ring, and which is linked via C), all of these cyclic groups being optionally substituted by (a) 1-3 COOH, halo, CN, mercapto, CHO, pyridyl, phenyl, CF3, NO2, TO, T', TS or Ac, or (b) T or 2-6C alkenyl (themselves optionally substituted by phenyl); or a group of formula (i)-(iv): R -R = H, COOH, halo, CN, CHO, CF3, NO2, T or CONR R ; R , R = H, 1-4C alkyl or phenyl; R , R -R = H, 3-6C cycloalkylcarbonyl, 3-6C cycloalkyl, T', or 1-10C alkyl (optionally substituted by CN, CF3, halo, phenyl, OH, COOH, T', 6-10C aryl, 3-6C cycloalkyl, (CO)cNR R , R -NH-SO2-R , R R NSO2 or R S(O)d); c = 0 or 1; R -R = H, 1-4C alkyl or phenyl; or together with the nitrogen atom, these groups form a 5-6 membered saturated heterocycle which optionally contains a further N, O or S heteroatom, and which is optionally substituted on C or N by 1-3C alkyl or 1-3C acyl; R , R = H, 1-4C alkyl or phenyl; d = 0-2; R , R = 1-4C alkyl, benzyl, phenyl, tolyl, or 1-6C acyl (optionally substituted by CF3, CCl3 or OR ); R = H, T (optionally substituted by aryl containing up to 10C), or (CO)eNR R , NR -SO2R , R R NSO2 or R -S(O)f; e = 0 or 1; R -R = as R -R ; R , R = H, 1-4C alkyl or phenyl; f = 0-2; R , R = as R , R ; D = O or S(O)g; g = 0-2; E, L = O or S; G, M, T, Q = O, S or NR ; R = H or 1-5C alkyl; a, b = 1 or 2; R = C(=S)R , C(=NR )R , C(=O)-(CH2)hOR , CN, a group Q or C(R )=C(R )NO2: R = 1-7C alkyl, 3-6C cycloalkyl, phenyl or NR R ; R , R = H, 1-4C alkyl or phenyl; R = H, CN, 3-6C cycloalkyl, phenyl or 1-7C alkyl; R = H, 1-7C alkyl, phenyl, 3-6C cycloalkyl, or NR R ; R , R = H, 1-4C alkyl or phenyl; h = 1-4; R = T or benzyl; R , R = H or T; Q = a 5-7 membered, saturated, partially unsaturated, or unsaturated heterocycle, containing up to 3 heteroatoms (selected from N, O and/or S) and which is optionally substituted on C or N by benzyl, halo or 1-5C alkyl; T =1-6C alkyl; T' = 1-6C alkoxycarbonyl; and Ac = 1-6C acyl.</description><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</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>eNqFi8EKgkAURd20iOoXYj7AIDCIlq_xmQ903jDzBsSNSEyrKMH6_xTct7qHw7nr5OvD1QtJEMwVN9ByRTkZNuhTZR1r9F5xoaREcpNACw6E2KSLCh4VmFzZElwNGoOQhkppri17msuJjQAZMrf545CLbbJ69M8x7pbdJPsCRZeHOLy7OA79Pb7ip9NtdjpezpBlf4MfCYI4rw</recordid><startdate>19970813</startdate><enddate>19970813</enddate><creator>STOLLE ANDREAS DR</creator><creator>RUPPELT MARTIN DR</creator><creator>HABICH DIETER DR</creator><creator>RIEDL BERND DR</creator><creator>ENDERMANN RAINER DR</creator><creator>KROLL HEIN PETER DR</creator><creator>GUARNIERI WALTER DR</creator><creator>BARTEL STEPHAN DR</creator><scope>EVB</scope></search><sort><creationdate>19970813</creationdate><title>SUBSTITUTED OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF</title><author>STOLLE ANDREAS DR ; RUPPELT MARTIN DR ; HABICH DIETER DR ; RIEDL BERND DR ; ENDERMANN RAINER DR ; KROLL HEIN PETER DR ; GUARNIERI WALTER DR ; BARTEL STEPHAN DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CZ34097A33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1997</creationdate><topic>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM</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>STOLLE ANDREAS DR</creatorcontrib><creatorcontrib>RUPPELT MARTIN DR</creatorcontrib><creatorcontrib>HABICH DIETER DR</creatorcontrib><creatorcontrib>RIEDL BERND DR</creatorcontrib><creatorcontrib>ENDERMANN RAINER DR</creatorcontrib><creatorcontrib>KROLL HEIN PETER DR</creatorcontrib><creatorcontrib>GUARNIERI WALTER DR</creatorcontrib><creatorcontrib>BARTEL STEPHAN DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>STOLLE ANDREAS DR</au><au>RUPPELT MARTIN DR</au><au>HABICH DIETER DR</au><au>RIEDL BERND DR</au><au>ENDERMANN RAINER DR</au><au>KROLL HEIN PETER DR</au><au>GUARNIERI WALTER DR</au><au>BARTEL STEPHAN DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SUBSTITUTED OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF</title><date>1997-08-13</date><risdate>1997</risdate><abstract>Substituted oxazolidinone compounds of formula (I) and their salts are new. A = 6-membered aromatic heterocycle (containing at least one N and which is linked via C), a 6-membered, bi- or tricyclic aromatic heterocycle (containing at least one N and which is linked via C), beta -carbolin-3-yl, indolizinyl (linked via the 6-membered ring), or a 5-membered aromatic heterocycle (containing up to 3 N, O and/or S, which may also be fused to a benzene or naphthalene ring, and which is linked via C), all of these cyclic groups being optionally substituted by (a) 1-3 COOH, halo, CN, mercapto, CHO, pyridyl, phenyl, CF3, NO2, TO, T', TS or Ac, or (b) T or 2-6C alkenyl (themselves optionally substituted by phenyl); or a group of formula (i)-(iv): R -R = H, COOH, halo, CN, CHO, CF3, NO2, T or CONR R ; R , R = H, 1-4C alkyl or phenyl; R , R -R = H, 3-6C cycloalkylcarbonyl, 3-6C cycloalkyl, T', or 1-10C alkyl (optionally substituted by CN, CF3, halo, phenyl, OH, COOH, T', 6-10C aryl, 3-6C cycloalkyl, (CO)cNR R , R -NH-SO2-R , R R NSO2 or R S(O)d); c = 0 or 1; R -R = H, 1-4C alkyl or phenyl; or together with the nitrogen atom, these groups form a 5-6 membered saturated heterocycle which optionally contains a further N, O or S heteroatom, and which is optionally substituted on C or N by 1-3C alkyl or 1-3C acyl; R , R = H, 1-4C alkyl or phenyl; d = 0-2; R , R = 1-4C alkyl, benzyl, phenyl, tolyl, or 1-6C acyl (optionally substituted by CF3, CCl3 or OR ); R = H, T (optionally substituted by aryl containing up to 10C), or (CO)eNR R , NR -SO2R , R R NSO2 or R -S(O)f; e = 0 or 1; R -R = as R -R ; R , R = H, 1-4C alkyl or phenyl; f = 0-2; R , R = as R , R ; D = O or S(O)g; g = 0-2; E, L = O or S; G, M, T, Q = O, S or NR ; R = H or 1-5C alkyl; a, b = 1 or 2; R = C(=S)R , C(=NR )R , C(=O)-(CH2)hOR , CN, a group Q or C(R )=C(R )NO2: R = 1-7C alkyl, 3-6C cycloalkyl, phenyl or NR R ; R , R = H, 1-4C alkyl or phenyl; R = H, CN, 3-6C cycloalkyl, phenyl or 1-7C alkyl; R = H, 1-7C alkyl, phenyl, 3-6C cycloalkyl, or NR R ; R , R = H, 1-4C alkyl or phenyl; h = 1-4; R = T or benzyl; R , R = H or T; Q = a 5-7 membered, saturated, partially unsaturated, or unsaturated heterocycle, containing up to 3 heteroatoms (selected from N, O and/or S) and which is optionally substituted on C or N by benzyl, halo or 1-5C alkyl; T =1-6C alkyl; T' = 1-6C alkoxycarbonyl; and Ac = 1-6C acyl.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM
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 OXAZOLIDINONES, PROCESS OF THEIR PREPARATION, THEIR USE AND PHARMACEUTICAL COMPOSITION CONTAINING THEREOF
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