http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0019345-A1

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filingDate 1978-08-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8111513d3c6a5812efbee7b5c6aa8119
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_21c904eed0af8868b17a2cc7d9396e52
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publicationDate 1980-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0019345-A1
titleOfInvention Process for the preparation of a (D-alpha-amino-(p-hydroxyphenyl)-acetamido) group containing cephalosporanic acid derivatives
abstract Process for the preparation of [D-a-amino-(p- hydroxyphenyl)acetamido] groups containing cephalosporanic acid derivatives, comprising the acylation of a compound of the formulae:n wherein R,, R 2 and R 3 representthe same or a different group and may be selected from a lower alkyl, benzyl, cycloalkyl or. phenyl-group and preferably lower alkyl and more preferably a methyl group an wherein X represents a residue selected from the group consisting of hydrogen, acetoxy or a five-membered heterocyclic thio residue, containing heteroatoms selected from nitrogen, oxygen, and/or sulphur and optionally substituted by lower alkyl and wherein an eventually present -NH- radical has optionally been silylated, which compound is previously prepared by the reaction of 7-aminocephalosporanic acid or its 3-methyl modifications with at least one equivalent and preferably about two with respect to other 3-methyl modifications of 7-ACA of a tri(lower)alkyl silyl groups supplying agent in a dry, inert, water insoluble solvent, such as methylene chloride, by rapid mixing of a pre-cooled solution of the compound offormulae I and Il with a pre-cooled reaction mixture of at least an equimolecular amount of a compound of the formulan n wherein R 4 represents lower alkyl and preferably methyl, R 5 represents hydrogen or lower alkyl and preferably methyl, R 6 represents lower alkoxy and preferably methoxy, nand R 7 represents lower alkoxy and preferably methoxy, previously prepared from the corresponding Dane salt and an acid chloride under anhydrous conditions in the presence of a tertiary amine as catalyst, such as N-methylmorpholine in a dry, inert, water insoluble, organic solvent such as methylene chloride mixed with a co-solvent or methyl isobutylketone or tetrahydrofuran optionally mixed with a co-solvent, and the continuation of the reaction at a temperature of -10°C or lower and preferably from -20°C to -30°C whereafter the desired compound is recovered by usual methods.
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priorityDate 1977-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID86738798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226399517
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13050420
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128421438
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559526
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128580662
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID411555350
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13475828
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226420206
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129812025
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID31374
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558806
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6344
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419531515
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID232605783
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12302722
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12437
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID164602

Total number of triples: 311.