SYNTHESIS AND CRYSTALLINE FORMS OF NPY5 ANTAGONIST
The present invention relates to a process for producing crystalline trans-N-[l-(2-fluorophenyl)- S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide and novel salts, hydrates and polymorphs thereof. L'invention concerne un procédé pour produire du trans-N-[...
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creator | FERLITA, RUSSELL, R ISHIKAWA, MAKOTO WANG, YALING NONOYAMA, NOBUAKI KATO, SHINJI HAGA, YUJI KAMEI, KEISUKE SATAKE, NOBUYA KOJIMA, HISAKI MOMENT, AARON WENSLOW, ROBERT, M WEISSMAN, STEVEN, A SHIGEMORI, KAZUKI WADA, TOSHIHIRO |
description | The present invention relates to a process for producing crystalline trans-N-[l-(2-fluorophenyl)- S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide and novel salts, hydrates and polymorphs thereof.
L'invention concerne un procédé pour produire du trans-N-[l-(2-fluorophényl)-S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide cristallin et de nouveaux sels, hydrates et polymorphes de celui-ci. |
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L'invention concerne un procédé pour produire du trans-N-[l-(2-fluorophényl)-S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide cristallin et de nouveaux sels, hydrates et polymorphes de celui-ci.</description><language>eng ; fre</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>2007</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=20070503&DB=EPODOC&CC=WO&NR=2007016028A3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20070503&DB=EPODOC&CC=WO&NR=2007016028A3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>FERLITA, RUSSELL, R</creatorcontrib><creatorcontrib>ISHIKAWA, MAKOTO</creatorcontrib><creatorcontrib>WANG, YALING</creatorcontrib><creatorcontrib>NONOYAMA, NOBUAKI</creatorcontrib><creatorcontrib>KATO, SHINJI</creatorcontrib><creatorcontrib>HAGA, YUJI</creatorcontrib><creatorcontrib>KAMEI, KEISUKE</creatorcontrib><creatorcontrib>SATAKE, NOBUYA</creatorcontrib><creatorcontrib>KOJIMA, HISAKI</creatorcontrib><creatorcontrib>MOMENT, AARON</creatorcontrib><creatorcontrib>WENSLOW, ROBERT, M</creatorcontrib><creatorcontrib>WEISSMAN, STEVEN, A</creatorcontrib><creatorcontrib>SHIGEMORI, KAZUKI</creatorcontrib><creatorcontrib>WADA, TOSHIHIRO</creatorcontrib><title>SYNTHESIS AND CRYSTALLINE FORMS OF NPY5 ANTAGONIST</title><description>The present invention relates to a process for producing crystalline trans-N-[l-(2-fluorophenyl)- S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide and novel salts, hydrates and polymorphs thereof.
L'invention concerne un procédé pour produire du trans-N-[l-(2-fluorophényl)-S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide cristallin et de nouveaux sels, hydrates et polymorphes de celui-ci.</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><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2007</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDAKjvQL8XAN9gxWcPRzUXAOigwOcfTx8fRzVXDzD_INVvB3U_ALiDQFyoY4uvv7eQaH8DCwpiXmFKfyQmluBmU31xBnD93Ugvz41OKCxOTUvNSS-HB_IwMDcwNDMwMjC0djY-JUAQAsmCfo</recordid><startdate>20070503</startdate><enddate>20070503</enddate><creator>FERLITA, RUSSELL, R</creator><creator>ISHIKAWA, MAKOTO</creator><creator>WANG, YALING</creator><creator>NONOYAMA, NOBUAKI</creator><creator>KATO, SHINJI</creator><creator>HAGA, YUJI</creator><creator>KAMEI, KEISUKE</creator><creator>SATAKE, NOBUYA</creator><creator>KOJIMA, HISAKI</creator><creator>MOMENT, AARON</creator><creator>WENSLOW, ROBERT, M</creator><creator>WEISSMAN, STEVEN, A</creator><creator>SHIGEMORI, KAZUKI</creator><creator>WADA, TOSHIHIRO</creator><scope>EVB</scope></search><sort><creationdate>20070503</creationdate><title>SYNTHESIS AND CRYSTALLINE FORMS OF NPY5 ANTAGONIST</title><author>FERLITA, RUSSELL, R ; ISHIKAWA, MAKOTO ; WANG, YALING ; NONOYAMA, NOBUAKI ; KATO, SHINJI ; HAGA, YUJI ; KAMEI, KEISUKE ; SATAKE, NOBUYA ; KOJIMA, HISAKI ; MOMENT, AARON ; WENSLOW, ROBERT, M ; WEISSMAN, STEVEN, A ; SHIGEMORI, KAZUKI ; WADA, TOSHIHIRO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_WO2007016028A33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2007</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><toplevel>online_resources</toplevel><creatorcontrib>FERLITA, RUSSELL, R</creatorcontrib><creatorcontrib>ISHIKAWA, MAKOTO</creatorcontrib><creatorcontrib>WANG, YALING</creatorcontrib><creatorcontrib>NONOYAMA, NOBUAKI</creatorcontrib><creatorcontrib>KATO, SHINJI</creatorcontrib><creatorcontrib>HAGA, YUJI</creatorcontrib><creatorcontrib>KAMEI, KEISUKE</creatorcontrib><creatorcontrib>SATAKE, NOBUYA</creatorcontrib><creatorcontrib>KOJIMA, HISAKI</creatorcontrib><creatorcontrib>MOMENT, AARON</creatorcontrib><creatorcontrib>WENSLOW, ROBERT, M</creatorcontrib><creatorcontrib>WEISSMAN, STEVEN, A</creatorcontrib><creatorcontrib>SHIGEMORI, KAZUKI</creatorcontrib><creatorcontrib>WADA, TOSHIHIRO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>FERLITA, RUSSELL, R</au><au>ISHIKAWA, MAKOTO</au><au>WANG, YALING</au><au>NONOYAMA, NOBUAKI</au><au>KATO, SHINJI</au><au>HAGA, YUJI</au><au>KAMEI, KEISUKE</au><au>SATAKE, NOBUYA</au><au>KOJIMA, HISAKI</au><au>MOMENT, AARON</au><au>WENSLOW, ROBERT, M</au><au>WEISSMAN, STEVEN, A</au><au>SHIGEMORI, KAZUKI</au><au>WADA, TOSHIHIRO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>SYNTHESIS AND CRYSTALLINE FORMS OF NPY5 ANTAGONIST</title><date>2007-05-03</date><risdate>2007</risdate><abstract>The present invention relates to a process for producing crystalline trans-N-[l-(2-fluorophenyl)- S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide and novel salts, hydrates and polymorphs thereof.
L'invention concerne un procédé pour produire du trans-N-[l-(2-fluorophényl)-S-pyrazoly]-3-oxospiro[6-azaisobenzofuran-1(3H),1'-cyclohexane]-4'-carboxamide cristallin et de nouveaux sels, hydrates et polymorphes de celui-ci.</abstract><oa>free_for_read</oa></addata></record> |
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title | SYNTHESIS AND CRYSTALLINE FORMS OF NPY5 ANTAGONIST |
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