3-HETEROCYCLIC THIOMETHYLCEPHALOSPORINS

1363833 3-Triazolylthiomethyl cephalsporins SMITHKLINE CORP 21 Feb 1973 [14 June 1972 15 Sept 1972] 8511/73 Headings C2A and C2C Novel cephalosporins having the Formula (I) wherein R is 1,2,3-triazolyl which may be substituted with 1 or 2 groups selected from C 1 -C 4 alkyl and trifluoromethyl are p...

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Hauptverfasser: JOHN RUSSEL EUGENE HOOVER, GEORGE LAWRENCE DUNN
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creator JOHN RUSSEL EUGENE HOOVER
GEORGE LAWRENCE DUNN
description 1363833 3-Triazolylthiomethyl cephalsporins SMITHKLINE CORP 21 Feb 1973 [14 June 1972 15 Sept 1972] 8511/73 Headings C2A and C2C Novel cephalosporins having the Formula (I) wherein R is 1,2,3-triazolyl which may be substituted with 1 or 2 groups selected from C 1 -C 4 alkyl and trifluoromethyl are prepared by (a) N-acylating an appropriate 7-amino-3- (1,2,3 - triazolylthiomethyl) - cephem - carboxylic acid with an amino-protected phydroxyphenylglycine or N-acylating derivative thereof; or (b) reacting. 7-α-amino-p-hydroxyphenylacetamidocephalosporanic acid having the α-amino group protected, with an appropriate mercaptomethyl-1,2,3-triazole. Alternatively 7-aminocephalosporanic acid may be reacted according to both of (a) and (b). The amino-protecting group is then removed to give the compound of formula (I). The inventive compounds (I) may be used in pharmaceutical compositions having antibiotic activity, admixed with a pharmaceutical diluent or carrier. The sodium salt of 5-mercapto-4-methyl-1,2,3- triazole is prepared by refluxing 5-benzamido-4- methyl-1,2,3-thiadiazole with aqueous NaOH, and treating an ethyl acetate extract of the product with sodium 2-ethylhexanoate to precipitate the said sodium salt.
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Alternatively 7-aminocephalosporanic acid may be reacted according to both of (a) and (b). The amino-protecting group is then removed to give the compound of formula (I). The inventive compounds (I) may be used in pharmaceutical compositions having antibiotic activity, admixed with a pharmaceutical diluent or carrier. The sodium salt of 5-mercapto-4-methyl-1,2,3- triazole is prepared by refluxing 5-benzamido-4- methyl-1,2,3-thiadiazole with aqueous NaOH, and treating an ethyl acetate extract of the product with sodium 2-ethylhexanoate to precipitate the said sodium salt.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; HUMAN NECESSITIES ; HYGIENE ; MEDICAL OR VETERINARY SCIENCE ; METALLURGY ; ORGANIC CHEMISTRY ; PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES ; SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS</subject><creationdate>1974</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=19740822&amp;DB=EPODOC&amp;CC=AU&amp;NR=5234573A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19740822&amp;DB=EPODOC&amp;CC=AU&amp;NR=5234573A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>JOHN RUSSEL EUGENE HOOVER</creatorcontrib><creatorcontrib>GEORGE LAWRENCE DUNN</creatorcontrib><title>3-HETEROCYCLIC THIOMETHYLCEPHALOSPORINS</title><description>1363833 3-Triazolylthiomethyl cephalsporins SMITHKLINE CORP 21 Feb 1973 [14 June 1972 15 Sept 1972] 8511/73 Headings C2A and C2C Novel cephalosporins having the Formula (I) wherein R is 1,2,3-triazolyl which may be substituted with 1 or 2 groups selected from C 1 -C 4 alkyl and trifluoromethyl are prepared by (a) N-acylating an appropriate 7-amino-3- (1,2,3 - triazolylthiomethyl) - cephem - carboxylic acid with an amino-protected phydroxyphenylglycine or N-acylating derivative thereof; or (b) reacting. 7-α-amino-p-hydroxyphenylacetamidocephalosporanic acid having the α-amino group protected, with an appropriate mercaptomethyl-1,2,3-triazole. 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Alternatively 7-aminocephalosporanic acid may be reacted according to both of (a) and (b). The amino-protecting group is then removed to give the compound of formula (I). The inventive compounds (I) may be used in pharmaceutical compositions having antibiotic activity, admixed with a pharmaceutical diluent or carrier. The sodium salt of 5-mercapto-4-methyl-1,2,3- triazole is prepared by refluxing 5-benzamido-4- methyl-1,2,3-thiadiazole with aqueous NaOH, and treating an ethyl acetate extract of the product with sodium 2-ethylhexanoate to precipitate the said sodium salt.</abstract><oa>free_for_read</oa></addata></record>
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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
SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS ORMEDICINAL PREPARATIONS
title 3-HETEROCYCLIC THIOMETHYLCEPHALOSPORINS
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