PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS

Quinolone carboxylic esters of general formula (II) are hydrolyzed to form quinolone carboxylic acids of general formula (I): the method comprises the step A): A) reacting compounds of formula (II) with a mixture that comprises acetic acid, sulfuric acid and water. In step A), = 30 to = 40 mol aceti...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: BERWE, Mathias, DIETZEL, Antje, FEY, Peter, WIRTHS, J”rg, LONGERICH, Markus, WISCHNAT, Ralf
Format: Patent
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator BERWE, Mathias
DIETZEL, Antje
FEY, Peter
WIRTHS, J”rg
LONGERICH, Markus
WISCHNAT, Ralf
description Quinolone carboxylic esters of general formula (II) are hydrolyzed to form quinolone carboxylic acids of general formula (I): the method comprises the step A): A) reacting compounds of formula (II) with a mixture that comprises acetic acid, sulfuric acid and water. In step A), = 30 to = 40 mol acetic acid, = 0.3 to = 1 mol sulfuric acid and = 0.9 to = 2.5 mol water are used per mol of compounds of formula (II). The process according to the invention is particularly suitable for the synthesis of the intermediate (I) in the synthesis of pradofloxacin.
format Patent
fullrecord <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_PH12020551750A1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>PH12020551750A1</sourcerecordid><originalsourceid>FETCH-epo_espacenet_PH12020551750A13</originalsourceid><addsrcrecordid>eNrjZLAMCPJ3dg0OVnDzD1II8XBV8Ih0CfL3iQz2DFbwd1MIDPX08_fx93NVcHYMcvKPiPTxdFZwDQ5xDQrmYWBNS8wpTuWF0twMKm6uIc4euqkF-fGpxQWJyal5qSXxAR6GRgZGBqamhuamBo6GxkQqAwCkUipE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS</title><source>esp@cenet</source><creator>BERWE, Mathias ; DIETZEL, Antje ; FEY, Peter ; WIRTHS, J”rg ; LONGERICH, Markus ; WISCHNAT, Ralf</creator><creatorcontrib>BERWE, Mathias ; DIETZEL, Antje ; FEY, Peter ; WIRTHS, J”rg ; LONGERICH, Markus ; WISCHNAT, Ralf</creatorcontrib><description>Quinolone carboxylic esters of general formula (II) are hydrolyzed to form quinolone carboxylic acids of general formula (I): the method comprises the step A): A) reacting compounds of formula (II) with a mixture that comprises acetic acid, sulfuric acid and water. In step A), = 30 to = 40 mol acetic acid, = 0.3 to = 1 mol sulfuric acid and = 0.9 to = 2.5 mol water are used per mol of compounds of formula (II). The process according to the invention is particularly suitable for the synthesis of the intermediate (I) in the synthesis of pradofloxacin.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2021</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=20210726&amp;DB=EPODOC&amp;CC=PH&amp;NR=12020551750A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,778,883,25547,76298</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20210726&amp;DB=EPODOC&amp;CC=PH&amp;NR=12020551750A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>BERWE, Mathias</creatorcontrib><creatorcontrib>DIETZEL, Antje</creatorcontrib><creatorcontrib>FEY, Peter</creatorcontrib><creatorcontrib>WIRTHS, J”rg</creatorcontrib><creatorcontrib>LONGERICH, Markus</creatorcontrib><creatorcontrib>WISCHNAT, Ralf</creatorcontrib><title>PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS</title><description>Quinolone carboxylic esters of general formula (II) are hydrolyzed to form quinolone carboxylic acids of general formula (I): the method comprises the step A): A) reacting compounds of formula (II) with a mixture that comprises acetic acid, sulfuric acid and water. In step A), = 30 to = 40 mol acetic acid, = 0.3 to = 1 mol sulfuric acid and = 0.9 to = 2.5 mol water are used per mol of compounds of formula (II). The process according to the invention is particularly suitable for the synthesis of the intermediate (I) in the synthesis of pradofloxacin.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2021</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZLAMCPJ3dg0OVnDzD1II8XBV8Ih0CfL3iQz2DFbwd1MIDPX08_fx93NVcHYMcvKPiPTxdFZwDQ5xDQrmYWBNS8wpTuWF0twMKm6uIc4euqkF-fGpxQWJyal5qSXxAR6GRgZGBqamhuamBo6GxkQqAwCkUipE</recordid><startdate>20210726</startdate><enddate>20210726</enddate><creator>BERWE, Mathias</creator><creator>DIETZEL, Antje</creator><creator>FEY, Peter</creator><creator>WIRTHS, J”rg</creator><creator>LONGERICH, Markus</creator><creator>WISCHNAT, Ralf</creator><scope>EVB</scope></search><sort><creationdate>20210726</creationdate><title>PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS</title><author>BERWE, Mathias ; DIETZEL, Antje ; FEY, Peter ; WIRTHS, J”rg ; LONGERICH, Markus ; WISCHNAT, Ralf</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_PH12020551750A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>2021</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>BERWE, Mathias</creatorcontrib><creatorcontrib>DIETZEL, Antje</creatorcontrib><creatorcontrib>FEY, Peter</creatorcontrib><creatorcontrib>WIRTHS, J”rg</creatorcontrib><creatorcontrib>LONGERICH, Markus</creatorcontrib><creatorcontrib>WISCHNAT, Ralf</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>BERWE, Mathias</au><au>DIETZEL, Antje</au><au>FEY, Peter</au><au>WIRTHS, J”rg</au><au>LONGERICH, Markus</au><au>WISCHNAT, Ralf</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS</title><date>2021-07-26</date><risdate>2021</risdate><abstract>Quinolone carboxylic esters of general formula (II) are hydrolyzed to form quinolone carboxylic acids of general formula (I): the method comprises the step A): A) reacting compounds of formula (II) with a mixture that comprises acetic acid, sulfuric acid and water. In step A), = 30 to = 40 mol acetic acid, = 0.3 to = 1 mol sulfuric acid and = 0.9 to = 2.5 mol water are used per mol of compounds of formula (II). The process according to the invention is particularly suitable for the synthesis of the intermediate (I) in the synthesis of pradofloxacin.</abstract><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier
ispartof
issn
language eng
recordid cdi_epo_espacenet_PH12020551750A1
source esp@cenet
subjects CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
title PROCESS FOR THE HYDROLYSIS OF QUINOLONE CARBOXYLIC ESTERS
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T08%3A04%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=BERWE,%20Mathias&rft.date=2021-07-26&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3EPH12020551750A1%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true