NEW PROCESS FOR PREPARING (-)-TRANS-N-p-FLUOROBENZOYLMETHYL-4-(p-FLUOROPHENYL)-3- 3,4-(METHYLENEDIOXY)PHENOXY]METHYL]-PIPERIDINE
The process consists in reacting (-)-trans-N-(p-fluorophenyl)-3-[[3,4-(methylenedioxy)phenoxy]methyl]-piperidine acetate with 2-chloro- or 2-bromo-4'-fluoroacetophenone, and the resulting compound can be isolated as a pharmaceutically acceptable addition salt by reaction with the corresponding...
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creator | FOGUET AMBROS RAFAEL GUBERT RIBERA SANTIAGO |
description | The process consists in reacting (-)-trans-N-(p-fluorophenyl)-3-[[3,4-(methylenedioxy)phenoxy]methyl]-piperidine acetate with 2-chloro- or 2-bromo-4'-fluoroacetophenone, and the resulting compound can be isolated as a pharmaceutically acceptable addition salt by reaction with the corresponding acid.
NUEVO PROCEDIMIENTO DE OBTENCION DE (-)-TRANS-N-P-FLUOROBENZOILMETIL-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA. CONSISTE EN HACER REACCIONAR ACETATO DE (-)-TRANS-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA CON 2-CLORO (O BROMO)-4''-FLUORO-ACETOFENONA, PUDIENDOSE AISLAR EL COMPUESTO RESULTANTE COMO SAL DE ADICION FARMACEUTICAMENTE ACEPTABLE POR REACCION CON EL ACIDO CORRESPONDIENTE. |
format | Patent |
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NUEVO PROCEDIMIENTO DE OBTENCION DE (-)-TRANS-N-P-FLUOROBENZOILMETIL-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA. CONSISTE EN HACER REACCIONAR ACETATO DE (-)-TRANS-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA CON 2-CLORO (O BROMO)-4''-FLUORO-ACETOFENONA, PUDIENDOSE AISLAR EL COMPUESTO RESULTANTE COMO SAL DE ADICION FARMACEUTICAMENTE ACEPTABLE POR REACCION CON EL ACIDO CORRESPONDIENTE.</description><edition>6</edition><language>eng ; spa</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES</subject><creationdate>1998</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=19980801&DB=EPODOC&CC=ES&NR=2117557A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19980801&DB=EPODOC&CC=ES&NR=2117557A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>FOGUET AMBROS RAFAEL</creatorcontrib><creatorcontrib>GUBERT RIBERA SANTIAGO</creatorcontrib><title>NEW PROCESS FOR PREPARING (-)-TRANS-N-p-FLUOROBENZOYLMETHYL-4-(p-FLUOROPHENYL)-3- 3,4-(METHYLENEDIOXY)PHENOXY]METHYL]-PIPERIDINE</title><description>The process consists in reacting (-)-trans-N-(p-fluorophenyl)-3-[[3,4-(methylenedioxy)phenoxy]methyl]-piperidine acetate with 2-chloro- or 2-bromo-4'-fluoroacetophenone, and the resulting compound can be isolated as a pharmaceutically acceptable addition salt by reaction with the corresponding acid.
NUEVO PROCEDIMIENTO DE OBTENCION DE (-)-TRANS-N-P-FLUOROBENZOILMETIL-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA. CONSISTE EN HACER REACCIONAR ACETATO DE (-)-TRANS-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA CON 2-CLORO (O BROMO)-4''-FLUORO-ACETOFENONA, PUDIENDOSE AISLAR EL COMPUESTO RESULTANTE COMO SAL DE ADICION FARMACEUTICAMENTE ACEPTABLE POR REACCION CON EL ACIDO CORRESPONDIENTE.</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>1998</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNisEKgkAURd20iOofZqnQW5iJa9NnDkxvhhmlJhCRmFZRgn1An55h7Vudyzl37r0Ij0xpmaExrJB63KhSzWnPfAig0ikZIOihELXUcod0llYcsCqtgC34v6BKJCsCiIBF69FPDyTMuTzZ4JNHNpNuQHGFmueccOnNrt1tcKsvFx4rsMpKcP2jdUPfXdzdPVs0mzBM4jhJw-iPyxsnjzxR</recordid><startdate>19980801</startdate><enddate>19980801</enddate><creator>FOGUET AMBROS RAFAEL</creator><creator>GUBERT RIBERA SANTIAGO</creator><scope>EVB</scope></search><sort><creationdate>19980801</creationdate><title>NEW PROCESS FOR PREPARING (-)-TRANS-N-p-FLUOROBENZOYLMETHYL-4-(p-FLUOROPHENYL)-3- 3,4-(METHYLENEDIOXY)PHENOXY]METHYL]-PIPERIDINE</title><author>FOGUET AMBROS RAFAEL ; GUBERT RIBERA SANTIAGO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ES2117557A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; spa</language><creationdate>1998</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>FOGUET AMBROS RAFAEL</creatorcontrib><creatorcontrib>GUBERT RIBERA SANTIAGO</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>FOGUET AMBROS RAFAEL</au><au>GUBERT RIBERA SANTIAGO</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>NEW PROCESS FOR PREPARING (-)-TRANS-N-p-FLUOROBENZOYLMETHYL-4-(p-FLUOROPHENYL)-3- 3,4-(METHYLENEDIOXY)PHENOXY]METHYL]-PIPERIDINE</title><date>1998-08-01</date><risdate>1998</risdate><abstract>The process consists in reacting (-)-trans-N-(p-fluorophenyl)-3-[[3,4-(methylenedioxy)phenoxy]methyl]-piperidine acetate with 2-chloro- or 2-bromo-4'-fluoroacetophenone, and the resulting compound can be isolated as a pharmaceutically acceptable addition salt by reaction with the corresponding acid.
NUEVO PROCEDIMIENTO DE OBTENCION DE (-)-TRANS-N-P-FLUOROBENZOILMETIL-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA. CONSISTE EN HACER REACCIONAR ACETATO DE (-)-TRANS-4-(P-FLUOROFENIL)-3-[[3,4-(METILENDIOXI)FENOXI]METIL]-PIPERIDINA CON 2-CLORO (O BROMO)-4''-FLUORO-ACETOFENONA, PUDIENDOSE AISLAR EL COMPUESTO RESULTANTE COMO SAL DE ADICION FARMACEUTICAMENTE ACEPTABLE POR REACCION CON EL ACIDO CORRESPONDIENTE.</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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language | eng ; spa |
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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 |
title | NEW PROCESS FOR PREPARING (-)-TRANS-N-p-FLUOROBENZOYLMETHYL-4-(p-FLUOROPHENYL)-3- 3,4-(METHYLENEDIOXY)PHENOXY]METHYL]-PIPERIDINE |
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