Process for preparation of beta -lactam derivatives
A process for preparing compounds of the formula I: (I) wherein X is sulphur, oxygen, methylene or sulphinyl (R or S configuration), R3 is hydrogen or methoxy, R4 is an optionally substituted (1-4C)alky group, Y is hydrogen or a carboxyl protecting group and Q is an optionally protected amino group...
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creator | LOTUS FRANK SNAPE EVAN W PEGG STEPHEN J |
description | A process for preparing compounds of the formula I: (I) wherein X is sulphur, oxygen, methylene or sulphinyl (R or S configuration), R3 is hydrogen or methoxy, R4 is an optionally substituted (1-4C)alky group, Y is hydrogen or a carboxyl protecting group and Q is an optionally protected amino group or an acylamino group, which comprises reacting a compound of formula (II) (II) with a compound of formula (III) (III) wherein R4 is as defined above and W and Z represent hydrogen atoms or a group or groups removable to yield the compound of formula (I). The compounds of the formula I are useful intermediates in the preparation of cephalosporin antibiotics. |
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fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_US4939250A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>US4939250A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_US4939250A3</originalsourceid><addsrcrecordid>eNrjZDAOKMpPTi0uVkjLL1IoKEotSCxKLMnMz1PIT1NISi1JVNDNSUwuScxVSEktyiwDSpWlFvMwsKYl5hSn8kJpbgZ5N9cQZw_d1IL8-NTigsTk1LzUkvjQYBNLY0sjUwNHY8IqAFBWK8U</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Process for preparation of beta -lactam derivatives</title><source>esp@cenet</source><creator>LOTUS; FRANK ; SNAPE; EVAN W ; PEGG; STEPHEN J</creator><creatorcontrib>LOTUS; FRANK ; SNAPE; EVAN W ; PEGG; STEPHEN J</creatorcontrib><description>A process for preparing compounds of the formula I: (I) wherein X is sulphur, oxygen, methylene or sulphinyl (R or S configuration), R3 is hydrogen or methoxy, R4 is an optionally substituted (1-4C)alky group, Y is hydrogen or a carboxyl protecting group and Q is an optionally protected amino group or an acylamino group, which comprises reacting a compound of formula (II) (II) with a compound of formula (III) (III) wherein R4 is as defined above and W and Z represent hydrogen atoms or a group or groups removable to yield the compound of formula (I). The compounds of the formula I are useful intermediates in the preparation of cephalosporin antibiotics.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1990</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=19900703&DB=EPODOC&CC=US&NR=4939250A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76289</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19900703&DB=EPODOC&CC=US&NR=4939250A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>LOTUS; FRANK</creatorcontrib><creatorcontrib>SNAPE; EVAN W</creatorcontrib><creatorcontrib>PEGG; STEPHEN J</creatorcontrib><title>Process for preparation of beta -lactam derivatives</title><description>A process for preparing compounds of the formula I: (I) wherein X is sulphur, oxygen, methylene or sulphinyl (R or S configuration), R3 is hydrogen or methoxy, R4 is an optionally substituted (1-4C)alky group, Y is hydrogen or a carboxyl protecting group and Q is an optionally protected amino group or an acylamino group, which comprises reacting a compound of formula (II) (II) with a compound of formula (III) (III) wherein R4 is as defined above and W and Z represent hydrogen atoms or a group or groups removable to yield the compound of formula (I). The compounds of the formula I are useful intermediates in the preparation of cephalosporin antibiotics.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1990</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDAOKMpPTi0uVkjLL1IoKEotSCxKLMnMz1PIT1NISi1JVNDNSUwuScxVSEktyiwDSpWlFvMwsKYl5hSn8kJpbgZ5N9cQZw_d1IL8-NTigsTk1LzUkvjQYBNLY0sjUwNHY8IqAFBWK8U</recordid><startdate>19900703</startdate><enddate>19900703</enddate><creator>LOTUS; FRANK</creator><creator>SNAPE; EVAN W</creator><creator>PEGG; STEPHEN J</creator><scope>EVB</scope></search><sort><creationdate>19900703</creationdate><title>Process for preparation of beta -lactam derivatives</title><author>LOTUS; FRANK ; SNAPE; EVAN W ; PEGG; STEPHEN J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US4939250A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1990</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>LOTUS; FRANK</creatorcontrib><creatorcontrib>SNAPE; EVAN W</creatorcontrib><creatorcontrib>PEGG; STEPHEN J</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LOTUS; FRANK</au><au>SNAPE; EVAN W</au><au>PEGG; STEPHEN J</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for preparation of beta -lactam derivatives</title><date>1990-07-03</date><risdate>1990</risdate><abstract>A process for preparing compounds of the formula I: (I) wherein X is sulphur, oxygen, methylene or sulphinyl (R or S configuration), R3 is hydrogen or methoxy, R4 is an optionally substituted (1-4C)alky group, Y is hydrogen or a carboxyl protecting group and Q is an optionally protected amino group or an acylamino group, which comprises reacting a compound of formula (II) (II) with a compound of formula (III) (III) wherein R4 is as defined above and W and Z represent hydrogen atoms or a group or groups removable to yield the compound of formula (I). The compounds of the formula I are useful intermediates in the preparation of cephalosporin antibiotics.</abstract><oa>free_for_read</oa></addata></record> |
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title | Process for preparation of beta -lactam derivatives |
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