http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1466710-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24aca9ded2638ea793d05360dde7a4a0
classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-18
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-04
filingDate 1974-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1977-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1466710-A
titleOfInvention Process for producing cephalosporin intermediates
abstract 1466710 3-Methyl-7-amino-cephem-4-carboxylic acids SUMITOMO CHEMICAL CO Ltd 29 Nov 1974 [29 Nov 1973] 51912/74 Headings C2C and C2P A cephalosporanic acid derivative of the Formula (I) wherein R 2 is an H atom or an ester protective group, is produced by reacting a phosphoramide derivative of Formula (II) wherein R 1 is C 1-4 alkyl, with a phosphorus acid, including orthophosphoric acid, phosphorous acid, phosphonic acid or phosphinic acid and the esters and anhydrides thereof. 2,2,2 - Trichloroethyl - 6# - dimethyl - phosphoramidopenicillanate 1-oxide is obtained by reacting 2,2,2-trichloroethyl-6#-(phenyl-acetamido)-penicillanate 1-oxide with PCl 5 in the presence of dimethylaniline and subsequently treating with methanol; the product is heated in the presence of pyridinium dichloromethane phosphonate to yield 2,2,2-trichloroethyl-3- methyl - 7# - dimethylphosphoramido - 3 - cephem - 4 - carboxylate; phenacyl 6 - aminopenicillanate hydrochloride is reacted with dimethylchlorophosphate in the presence of triethylamine and further with m-chloroperbenzoic acid to give phenacyl 6#-dimethylphosphoramidopenicillanate 1-oxide which on heating with pyridinium dichloromethanephosphonate yields phenacyl 3-methyl-7#-dimethylphosphoramido - ceph - 3 - em - 4 - carboxylate; phenacyl 6# - dimethylphosphoramidopenicillanate - 1- oxide was also obtained by first forming phenacyl 6#-aminopenicillanate 1-oxide and reacting with dimethyl chlorophosphate in the presence of diethylaniline.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0018155-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0018155-A3
priorityDate 1973-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419557048
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID313
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426644557
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559532
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419524285
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID22497
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407330845
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419553602
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1004
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70297
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24404
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID949
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448690866
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7057887
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411932836
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415807220
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411550722
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457766247
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419515849
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419579525
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419547221
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8471
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454715845
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID101863
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13475828
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID20330760
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID68134367
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7061
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID887
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419508115
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458393365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3084169
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12302722
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451

Total number of triples: 50.