2,3,4,5-TETRAHYDRO-1,4-BENZOTHIAZEPINE DERIVATIVES OPTIONALLY SUBSTITUTED IN POSITION-6 BY METHYL, FLUORO OR CHLORO
PCT No. PCT/EP93/03123 Sec. 371 Date May 3, 1995 Sec. 102(e) Date May 3, 1995 PCT Filed Nov. 6, 1993 PCT Pub. No. WO94/11360 PCT Pub. Date May 26, 1994Compounds of formula I I in which n=0, 1 or 2; R1, R2, R6 and R7 independently represent H or alkyl (optionally substituted by one or more halo); R3...
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creator | JEFFERY, JAMES EDWARD SARGENT, BRUCE JEREMY HOUSLEY, JOHN ROSINDALE NICHOL, KENNETH JOHN |
description | PCT No. PCT/EP93/03123 Sec. 371 Date May 3, 1995 Sec. 102(e) Date May 3, 1995 PCT Filed Nov. 6, 1993 PCT Pub. No. WO94/11360 PCT Pub. Date May 26, 1994Compounds of formula I I in which n=0, 1 or 2; R1, R2, R6 and R7 independently represent H or alkyl (optionally substituted by one or more halo); R3 and R4 independently represent H or alkyl or together represent a group of formula =NR12 where R12 represents H, hydroxy, alkyl, phenyl or alkoxy; each alkyl, phenyl and alkoxy being optionally substituted with one or more halo; R5 represents: (a) H, (b) alkyl, (c) a group of formula -COR13 in which R13 is H, alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo), or (d) a group of formula -S(O)pR14 in which p=1 or 2 and R14 is alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo); each alkyl and phenyl optionally substituted with one or more halo; and R8 to R11 independently represent H, halo, cyano, nitro, alkyl alkoxy, alkanoyl, carboxy, alkanoyloxy, carbamoyl (optionally substituted with alkyl or sulphamoyl (optionally substituted with alkyl of 1 to 4 carbon atoms); each alkyl, alkoxy, alkanoyl or alkanoyloxy optionally substituted with one or more halo; have utility in the treatment of seizures and/or neurological disorders such as epilepsy and/or as neuroprotective agents to protect against conditions such as stroke. |
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No. WO94/11360 PCT Pub. Date May 26, 1994Compounds of formula I I in which n=0, 1 or 2; R1, R2, R6 and R7 independently represent H or alkyl (optionally substituted by one or more halo); R3 and R4 independently represent H or alkyl or together represent a group of formula =NR12 where R12 represents H, hydroxy, alkyl, phenyl or alkoxy; each alkyl, phenyl and alkoxy being optionally substituted with one or more halo; R5 represents: (a) H, (b) alkyl, (c) a group of formula -COR13 in which R13 is H, alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo), or (d) a group of formula -S(O)pR14 in which p=1 or 2 and R14 is alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo); each alkyl and phenyl optionally substituted with one or more halo; and R8 to R11 independently represent H, halo, cyano, nitro, alkyl alkoxy, alkanoyl, carboxy, alkanoyloxy, carbamoyl (optionally substituted with alkyl or sulphamoyl (optionally substituted with alkyl of 1 to 4 carbon atoms); each alkyl, alkoxy, alkanoyl or alkanoyloxy optionally substituted with one or more halo; have utility in the treatment of seizures and/or neurological disorders such as epilepsy and/or as neuroprotective agents to protect against conditions such as stroke.</description><edition>6</edition><language>eng</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>1996</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=19961028&DB=EPODOC&CC=NZ&NR=257843A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19961028&DB=EPODOC&CC=NZ&NR=257843A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JEFFERY, JAMES EDWARD</creatorcontrib><creatorcontrib>SARGENT, BRUCE JEREMY</creatorcontrib><creatorcontrib>HOUSLEY, JOHN ROSINDALE</creatorcontrib><creatorcontrib>NICHOL, KENNETH JOHN</creatorcontrib><title>2,3,4,5-TETRAHYDRO-1,4-BENZOTHIAZEPINE DERIVATIVES OPTIONALLY SUBSTITUTED IN POSITION-6 BY METHYL, FLUORO OR CHLORO</title><description>PCT No. PCT/EP93/03123 Sec. 371 Date May 3, 1995 Sec. 102(e) Date May 3, 1995 PCT Filed Nov. 6, 1993 PCT Pub. No. WO94/11360 PCT Pub. Date May 26, 1994Compounds of formula I I in which n=0, 1 or 2; R1, R2, R6 and R7 independently represent H or alkyl (optionally substituted by one or more halo); R3 and R4 independently represent H or alkyl or together represent a group of formula =NR12 where R12 represents H, hydroxy, alkyl, phenyl or alkoxy; each alkyl, phenyl and alkoxy being optionally substituted with one or more halo; R5 represents: (a) H, (b) alkyl, (c) a group of formula -COR13 in which R13 is H, alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo), or (d) a group of formula -S(O)pR14 in which p=1 or 2 and R14 is alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo); each alkyl and phenyl optionally substituted with one or more halo; and R8 to R11 independently represent H, halo, cyano, nitro, alkyl alkoxy, alkanoyl, carboxy, alkanoyloxy, carbamoyl (optionally substituted with alkyl or sulphamoyl (optionally substituted with alkyl of 1 to 4 carbon atoms); each alkyl, alkoxy, alkanoyl or alkanoyloxy optionally substituted with one or more halo; have utility in the treatment of seizures and/or neurological disorders such as epilepsy and/or as neuroprotective agents to protect against conditions such as stroke.</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>1996</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqFirsKwjAUQLs4iPoLcj8gGexDXdP2lgRiUpLbQrqUInESLdT_RwV3p3PgnHWypCxjOSs4ITkhQ-0sP7Ccl2gGS1KJAVtlEGp0qhekevRgW1LWCK0D-K70pKgjrEEZaK1X38aPUAa4IMmgGTS6s86CdVBJ_bFtsrpN9yXuftwk-wapkjzOzzEu83SNj_gazZAWp3Oeiezv8AYHGDd0</recordid><startdate>19961028</startdate><enddate>19961028</enddate><creator>JEFFERY, JAMES EDWARD</creator><creator>SARGENT, BRUCE JEREMY</creator><creator>HOUSLEY, JOHN ROSINDALE</creator><creator>NICHOL, KENNETH JOHN</creator><scope>EVB</scope></search><sort><creationdate>19961028</creationdate><title>2,3,4,5-TETRAHYDRO-1,4-BENZOTHIAZEPINE DERIVATIVES OPTIONALLY SUBSTITUTED IN POSITION-6 BY METHYL, FLUORO OR CHLORO</title><author>JEFFERY, JAMES EDWARD ; SARGENT, BRUCE JEREMY ; HOUSLEY, JOHN ROSINDALE ; NICHOL, KENNETH JOHN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_NZ257843A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1996</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>JEFFERY, JAMES EDWARD</creatorcontrib><creatorcontrib>SARGENT, BRUCE JEREMY</creatorcontrib><creatorcontrib>HOUSLEY, JOHN ROSINDALE</creatorcontrib><creatorcontrib>NICHOL, KENNETH JOHN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>JEFFERY, JAMES EDWARD</au><au>SARGENT, BRUCE JEREMY</au><au>HOUSLEY, JOHN ROSINDALE</au><au>NICHOL, KENNETH JOHN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>2,3,4,5-TETRAHYDRO-1,4-BENZOTHIAZEPINE DERIVATIVES OPTIONALLY SUBSTITUTED IN POSITION-6 BY METHYL, FLUORO OR CHLORO</title><date>1996-10-28</date><risdate>1996</risdate><abstract>PCT No. PCT/EP93/03123 Sec. 371 Date May 3, 1995 Sec. 102(e) Date May 3, 1995 PCT Filed Nov. 6, 1993 PCT Pub. No. WO94/11360 PCT Pub. Date May 26, 1994Compounds of formula I I in which n=0, 1 or 2; R1, R2, R6 and R7 independently represent H or alkyl (optionally substituted by one or more halo); R3 and R4 independently represent H or alkyl or together represent a group of formula =NR12 where R12 represents H, hydroxy, alkyl, phenyl or alkoxy; each alkyl, phenyl and alkoxy being optionally substituted with one or more halo; R5 represents: (a) H, (b) alkyl, (c) a group of formula -COR13 in which R13 is H, alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo), or (d) a group of formula -S(O)pR14 in which p=1 or 2 and R14 is alkyl or phenyl, when R3 and R4 represent H or alkyl (optionally substituted with one or more halo); each alkyl and phenyl optionally substituted with one or more halo; and R8 to R11 independently represent H, halo, cyano, nitro, alkyl alkoxy, alkanoyl, carboxy, alkanoyloxy, carbamoyl (optionally substituted with alkyl or sulphamoyl (optionally substituted with alkyl of 1 to 4 carbon atoms); each alkyl, alkoxy, alkanoyl or alkanoyloxy optionally substituted with one or more halo; have utility in the treatment of seizures and/or neurological disorders such as epilepsy and/or as neuroprotective agents to protect against conditions such as stroke.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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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 | 2,3,4,5-TETRAHYDRO-1,4-BENZOTHIAZEPINE DERIVATIVES OPTIONALLY SUBSTITUTED IN POSITION-6 BY METHYL, FLUORO OR CHLORO |
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