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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C51-493
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D277-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D501-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C51-493
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-06
filingDate 1965-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14f03c889f0f53e1235adc1d90882e0b
publicationDate 1970-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-497460-A
titleOfInvention Process for the preparation of aminoformyl compounds
abstract Process for the prepn. of cpds. where ac = acyl; X = disubstd. C atom; Ra= an alcohol residue; Ro= H or an acyl. Intermediates in the prepn. of pharmaceuticals, particularly 7-acylaminocephalosporanic acids. To (III) obtained by addn. of 6 g. of the corresponding malic ester in 100 ml. MeOCH2CH2OMe to 400 ml. refluxing octane and removal of 240 ml. solvent is added 1 g. (IV) and the mixt. is refluxed for 9 hrs. Evapn. and extn. with C6H6 gives crude (V), 1.158 g. of which is chromatographed on 45 g. silica gel, to give mainly isomer A, (alpha)D-122 deg.
priorityDate 1965-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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