http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-497460-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_08621f74d1f2818b7712be84fb35735d |
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 |
Incoming Links
Total number of triples: 105.