PROCESS FOR PREPARATION OF OLOPATADINE HYDROCHLORIDE
Disclosed here is a process for preparation of compound 11 - (Z) - [3 - (Dimethylamino) propylidene] - 6, 11 - dihydrodibenz [b, e] oxepin -2 - yl - acetic acid (Olopatadine) and its pharmaceutically acceptable salt comprising reacting compound of Formula (XII) where R1 & R2 independently repres...
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creator | DESHMUKH, SANDIP, KACHARU KHABALE, SOMNATH PANANDIKAR, ADITI, MILIND NAIR, RANJEET RAMESAN, P., V |
description | Disclosed here is a process for preparation of compound 11 - (Z) - [3 - (Dimethylamino) propylidene] - 6, 11 - dihydrodibenz [b, e] oxepin -2 - yl - acetic acid (Olopatadine) and its pharmaceutically acceptable salt comprising reacting compound of Formula (XII) where R1 & R2 independently represent H, or C1 - C4 alkyl group; with 3-dimethylaminopropyl magnesium halide of Formula (XIII) where X is Chlorine, bromine or iodine.
L'invention concerne un procédé de préparation d'un composé d'acide 11-(Z)-[3-diméthylamino)propylidène]-6,11-dihydrodibenz[b,e]oxépin-2-yl-acétique (olopatadine) et de ses sels pharmaceutiquement acceptables. Le procédé consiste à mettre en réaction un composé de formule (XII) dans laquelle R1 et R2 représentent indépendamment H ou groupe alkyle C1-C4 avec un halogénure de 3-diméthylaminopropyl magnésium de formule (XIII) dans laquelle X est chlorure, brome ou iode. |
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L'invention concerne un procédé de préparation d'un composé d'acide 11-(Z)-[3-diméthylamino)propylidène]-6,11-dihydrodibenz[b,e]oxépin-2-yl-acétique (olopatadine) et de ses sels pharmaceutiquement acceptables. Le procédé consiste à mettre en réaction un composé de formule (XII) dans laquelle R1 et R2 représentent indépendamment H ou groupe alkyle C1-C4 avec un halogénure de 3-diméthylaminopropyl magnésium de formule (XIII) dans laquelle X est chlorure, brome ou iode.</description><language>eng ; fre</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2011</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=20110324&DB=EPODOC&CC=WO&NR=2011033532A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20110324&DB=EPODOC&CC=WO&NR=2011033532A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>DESHMUKH, SANDIP, KACHARU</creatorcontrib><creatorcontrib>KHABALE, SOMNATH</creatorcontrib><creatorcontrib>PANANDIKAR, ADITI, MILIND</creatorcontrib><creatorcontrib>NAIR, RANJEET</creatorcontrib><creatorcontrib>RAMESAN, P., V</creatorcontrib><title>PROCESS FOR PREPARATION OF OLOPATADINE HYDROCHLORIDE</title><description>Disclosed here is a process for preparation of compound 11 - (Z) - [3 - (Dimethylamino) propylidene] - 6, 11 - dihydrodibenz [b, e] oxepin -2 - yl - acetic acid (Olopatadine) and its pharmaceutically acceptable salt comprising reacting compound of Formula (XII) where R1 & R2 independently represent H, or C1 - C4 alkyl group; with 3-dimethylaminopropyl magnesium halide of Formula (XIII) where X is Chlorine, bromine or iodine.
L'invention concerne un procédé de préparation d'un composé d'acide 11-(Z)-[3-diméthylamino)propylidène]-6,11-dihydrodibenz[b,e]oxépin-2-yl-acétique (olopatadine) et de ses sels pharmaceutiquement acceptables. Le procédé consiste à mettre en réaction un composé de formule (XII) dans laquelle R1 et R2 représentent indépendamment H ou groupe alkyle C1-C4 avec un halogénure de 3-diméthylaminopropyl magnésium de formule (XIII) dans laquelle X est chlorure, brome ou iode.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2011</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDAJCPJ3dg0OVnDzD1IICHINcAxyDPH091Pwd1Pw9_EPcAxxdPH0c1XwiHQBKvTw8Q_ydHHlYWBNS8wpTuWF0twMym6uIc4euqkF-fGpxQWJyal5qSXx4f5GBoaGBsbGpsZGjobGxKkCAH4pKHM</recordid><startdate>20110324</startdate><enddate>20110324</enddate><creator>DESHMUKH, SANDIP, KACHARU</creator><creator>KHABALE, SOMNATH</creator><creator>PANANDIKAR, ADITI, MILIND</creator><creator>NAIR, RANJEET</creator><creator>RAMESAN, P., V</creator><scope>EVB</scope></search><sort><creationdate>20110324</creationdate><title>PROCESS FOR PREPARATION OF OLOPATADINE HYDROCHLORIDE</title><author>DESHMUKH, SANDIP, KACHARU ; KHABALE, SOMNATH ; PANANDIKAR, ADITI, MILIND ; NAIR, RANJEET ; RAMESAN, P., V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_WO2011033532A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre</language><creationdate>2011</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>DESHMUKH, SANDIP, KACHARU</creatorcontrib><creatorcontrib>KHABALE, SOMNATH</creatorcontrib><creatorcontrib>PANANDIKAR, ADITI, MILIND</creatorcontrib><creatorcontrib>NAIR, RANJEET</creatorcontrib><creatorcontrib>RAMESAN, P., V</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>DESHMUKH, SANDIP, KACHARU</au><au>KHABALE, SOMNATH</au><au>PANANDIKAR, ADITI, MILIND</au><au>NAIR, RANJEET</au><au>RAMESAN, P., V</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR PREPARATION OF OLOPATADINE HYDROCHLORIDE</title><date>2011-03-24</date><risdate>2011</risdate><abstract>Disclosed here is a process for preparation of compound 11 - (Z) - [3 - (Dimethylamino) propylidene] - 6, 11 - dihydrodibenz [b, e] oxepin -2 - yl - acetic acid (Olopatadine) and its pharmaceutically acceptable salt comprising reacting compound of Formula (XII) where R1 & R2 independently represent H, or C1 - C4 alkyl group; with 3-dimethylaminopropyl magnesium halide of Formula (XIII) where X is Chlorine, bromine or iodine.
L'invention concerne un procédé de préparation d'un composé d'acide 11-(Z)-[3-diméthylamino)propylidène]-6,11-dihydrodibenz[b,e]oxépin-2-yl-acétique (olopatadine) et de ses sels pharmaceutiquement acceptables. Le procédé consiste à mettre en réaction un composé de formule (XII) dans laquelle R1 et R2 représentent indépendamment H ou groupe alkyle C1-C4 avec un halogénure de 3-diméthylaminopropyl magnésium de formule (XIII) dans laquelle X est chlorure, brome ou iode.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | PROCESS FOR PREPARATION OF OLOPATADINE HYDROCHLORIDE |
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