Novel synthesis method of cefprozil
The invention belongs to the technical field of medicine synthesis and preparation and in particular relates to patent application of a novel cefprozil synthesis and preparation method. The method hasthe technical thought as follows: alkali substitution reaction is carried out on beta-lactam parent...
Gespeichert in:
Hauptverfasser: | , , , , , , , , , , |
---|---|
Format: | Patent |
Sprache: | chi ; 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 | YANG QIUYAN REN ZHEN NIAN BEILEI QIAN DAN CHENG YALI WU MINGSHU YANG MING WU YANJIE ZHANG CHUNSHENG CHEN JINCHUN WANG JUNCHEN |
description | The invention belongs to the technical field of medicine synthesis and preparation and in particular relates to patent application of a novel cefprozil synthesis and preparation method. The method hasthe technical thought as follows: alkali substitution reaction is carried out on beta-lactam parent nucleus(7-amin-3-(Z-prop-1-enyl)-4-cephalosporanic acid) in an aprotic solvent; then a branched-chain D-p-hydroxyphenylglycine derivative is added to carry out condensation reaction, so that cefprozil is prepared. Totally, the preparation method provided by the invention has the advantages of easiness for obtaining reaction raw materials, moderate reaction conditions and easiness for controlling; after the reaction is finished, the residue of main raw materials is relatively low, the cost pressure caused by the main raw materials can be greatly reduced and the yield of the cefprozil is relatively high; meanwhile, the method has a relatively simple process route and a high-quality cefprozilproduct can be obtained th |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN108440567A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN108440567A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN108440567A3</originalsourceid><addsrcrecordid>eNrjZFD2yy9LzVEorswryUgtzixWyE0tychPUchPU0hOTSsoyq_KzOFhYE1LzClO5YXS3AyKbq4hzh66qQX58anFBYnJqXmpJfHOfoYGFiYmBqZm5o7GxKgBAPcHJqI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Novel synthesis method of cefprozil</title><source>esp@cenet</source><creator>YANG QIUYAN ; REN ZHEN ; NIAN BEILEI ; QIAN DAN ; CHENG YALI ; WU MINGSHU ; YANG MING ; WU YANJIE ; ZHANG CHUNSHENG ; CHEN JINCHUN ; WANG JUNCHEN</creator><creatorcontrib>YANG QIUYAN ; REN ZHEN ; NIAN BEILEI ; QIAN DAN ; CHENG YALI ; WU MINGSHU ; YANG MING ; WU YANJIE ; ZHANG CHUNSHENG ; CHEN JINCHUN ; WANG JUNCHEN</creatorcontrib><description>The invention belongs to the technical field of medicine synthesis and preparation and in particular relates to patent application of a novel cefprozil synthesis and preparation method. The method hasthe technical thought as follows: alkali substitution reaction is carried out on beta-lactam parent nucleus(7-amin-3-(Z-prop-1-enyl)-4-cephalosporanic acid) in an aprotic solvent; then a branched-chain D-p-hydroxyphenylglycine derivative is added to carry out condensation reaction, so that cefprozil is prepared. Totally, the preparation method provided by the invention has the advantages of easiness for obtaining reaction raw materials, moderate reaction conditions and easiness for controlling; after the reaction is finished, the residue of main raw materials is relatively low, the cost pressure caused by the main raw materials can be greatly reduced and the yield of the cefprozil is relatively high; meanwhile, the method has a relatively simple process route and a high-quality cefprozilproduct can be obtained th</description><language>chi ; eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2018</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=20180824&DB=EPODOC&CC=CN&NR=108440567A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76318</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20180824&DB=EPODOC&CC=CN&NR=108440567A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>YANG QIUYAN</creatorcontrib><creatorcontrib>REN ZHEN</creatorcontrib><creatorcontrib>NIAN BEILEI</creatorcontrib><creatorcontrib>QIAN DAN</creatorcontrib><creatorcontrib>CHENG YALI</creatorcontrib><creatorcontrib>WU MINGSHU</creatorcontrib><creatorcontrib>YANG MING</creatorcontrib><creatorcontrib>WU YANJIE</creatorcontrib><creatorcontrib>ZHANG CHUNSHENG</creatorcontrib><creatorcontrib>CHEN JINCHUN</creatorcontrib><creatorcontrib>WANG JUNCHEN</creatorcontrib><title>Novel synthesis method of cefprozil</title><description>The invention belongs to the technical field of medicine synthesis and preparation and in particular relates to patent application of a novel cefprozil synthesis and preparation method. The method hasthe technical thought as follows: alkali substitution reaction is carried out on beta-lactam parent nucleus(7-amin-3-(Z-prop-1-enyl)-4-cephalosporanic acid) in an aprotic solvent; then a branched-chain D-p-hydroxyphenylglycine derivative is added to carry out condensation reaction, so that cefprozil is prepared. Totally, the preparation method provided by the invention has the advantages of easiness for obtaining reaction raw materials, moderate reaction conditions and easiness for controlling; after the reaction is finished, the residue of main raw materials is relatively low, the cost pressure caused by the main raw materials can be greatly reduced and the yield of the cefprozil is relatively high; meanwhile, the method has a relatively simple process route and a high-quality cefprozilproduct can be obtained th</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2018</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFD2yy9LzVEorswryUgtzixWyE0tychPUchPU0hOTSsoyq_KzOFhYE1LzClO5YXS3AyKbq4hzh66qQX58anFBYnJqXmpJfHOfoYGFiYmBqZm5o7GxKgBAPcHJqI</recordid><startdate>20180824</startdate><enddate>20180824</enddate><creator>YANG QIUYAN</creator><creator>REN ZHEN</creator><creator>NIAN BEILEI</creator><creator>QIAN DAN</creator><creator>CHENG YALI</creator><creator>WU MINGSHU</creator><creator>YANG MING</creator><creator>WU YANJIE</creator><creator>ZHANG CHUNSHENG</creator><creator>CHEN JINCHUN</creator><creator>WANG JUNCHEN</creator><scope>EVB</scope></search><sort><creationdate>20180824</creationdate><title>Novel synthesis method of cefprozil</title><author>YANG QIUYAN ; REN ZHEN ; NIAN BEILEI ; QIAN DAN ; CHENG YALI ; WU MINGSHU ; YANG MING ; WU YANJIE ; ZHANG CHUNSHENG ; CHEN JINCHUN ; WANG JUNCHEN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN108440567A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2018</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>YANG QIUYAN</creatorcontrib><creatorcontrib>REN ZHEN</creatorcontrib><creatorcontrib>NIAN BEILEI</creatorcontrib><creatorcontrib>QIAN DAN</creatorcontrib><creatorcontrib>CHENG YALI</creatorcontrib><creatorcontrib>WU MINGSHU</creatorcontrib><creatorcontrib>YANG MING</creatorcontrib><creatorcontrib>WU YANJIE</creatorcontrib><creatorcontrib>ZHANG CHUNSHENG</creatorcontrib><creatorcontrib>CHEN JINCHUN</creatorcontrib><creatorcontrib>WANG JUNCHEN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>YANG QIUYAN</au><au>REN ZHEN</au><au>NIAN BEILEI</au><au>QIAN DAN</au><au>CHENG YALI</au><au>WU MINGSHU</au><au>YANG MING</au><au>WU YANJIE</au><au>ZHANG CHUNSHENG</au><au>CHEN JINCHUN</au><au>WANG JUNCHEN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Novel synthesis method of cefprozil</title><date>2018-08-24</date><risdate>2018</risdate><abstract>The invention belongs to the technical field of medicine synthesis and preparation and in particular relates to patent application of a novel cefprozil synthesis and preparation method. The method hasthe technical thought as follows: alkali substitution reaction is carried out on beta-lactam parent nucleus(7-amin-3-(Z-prop-1-enyl)-4-cephalosporanic acid) in an aprotic solvent; then a branched-chain D-p-hydroxyphenylglycine derivative is added to carry out condensation reaction, so that cefprozil is prepared. Totally, the preparation method provided by the invention has the advantages of easiness for obtaining reaction raw materials, moderate reaction conditions and easiness for controlling; after the reaction is finished, the residue of main raw materials is relatively low, the cost pressure caused by the main raw materials can be greatly reduced and the yield of the cefprozil is relatively high; meanwhile, the method has a relatively simple process route and a high-quality cefprozilproduct can be obtained th</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | chi ; eng |
recordid | cdi_epo_espacenet_CN108440567A |
source | esp@cenet |
subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Novel synthesis method of cefprozil |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T23%3A30%3A42IST&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=YANG%20QIUYAN&rft.date=2018-08-24&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN108440567A%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 |