http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IE-42620-B1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_589e019870e8f74165d0734073a38d8e |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K49-0433 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D319-06 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C237-46 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-69 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-165 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K49-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D319-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-00 |
| filingDate | 1975-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1980-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | IE-42620-B1 |
| titleOfInvention | Non-ionic x-ray contras agents |
| abstract | 1472050 Triodobenzoyl compounds SAVAC AG 26 Nov 1975 [13 Dec 1974] 48620/75 Heading C2C [Also in Division A5] Novel compounds of Formula I wherein R is H or OH and C 3 H 5 (OH) 2 is -CH(CH 2 OH) 2 or -CH 2 CH(OH)CH 2 OH are prepared by reaction of a compound of Formula II wherein Y denotes hydrogen or iodine, Z denotes an amino group, a nitro group, an α-hydroxypropionylamino group or an α,#-dihydroxypropionylamino group, the or each hydroxyl group of either of which may be and if necessary is masked (i.e. protected) by easily reversible acylation, etherification or in the case of an α,#-dihydroxypropionylamino group acetalization or ketalization, and each -CO-X denotes a reactive functional derivative of a carboxylic acid group, with a dihydroxypropylamine, the hydroxyl groups of which may be, and if necessary are, masked by easily reversible acylation, etherification, acetalization or ketalization, reducing the 5-nitro group (where Z is nitro) to a 5-amino group, and after any reduction of the 5-nitro group, iodinating any of the groups Y on the aromatic nucleus which are hydrogen and acylating any 5-amino group, with a compound of the general formula (III) wherein R denotes hydrogen or hydroxyl, the or each hydroxyl group of which may be, and if necessary is, also masked by easily reversible acylation, etherification, acetalization or ketalization, and -CO-X denotes a reactive functional derivative of a carboxylic acid group, whereby there is formed a compound of general Formula (I) or a derivative with one or more hydroxyl groups masked by easily reversible acylation, etherification, acetalization or ketalization the masking groups being subsequently removed from the latter. |
| priorityDate | 1974-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 118.