http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-1943160-A1
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97a285d8ecd0184a7e5d89a1e4e07997 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D499-00 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D499-00 |
filingDate | 1969-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0b5b5cc5403472f136e1f3d092017886 |
publicationDate | 1971-03-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | DE-1943160-A1 |
titleOfInvention | 2-azetidiones |
abstract | Cpds. of formulae (I)-(III) where X="blocked" primary amino gp. e.g. phthalimido, tritylamino, o-nitrophenoxyacetamido, o-nitrophenylsulphenylamino, carbobenzoxyamino, formylamino, carbo-t-butoxyamino Note: only cpd. (II) is claimed, together with its acid addn. salts. (I) and (III) as intermediates in the synthesis of penicillins and cephalosporins (procedures given). (II) as intermediate to mothproofing agents and pickling inhibitors. 3-Phthalimido-4-mercapto-2-azetidinone is reacted with N2H4.H2O (1 equiv.) in dioxan at room temp. for 12 hr. HCl is added to ppt. phthalhydrazide, which is filtered off and the filtrate lyophilised to provide (II).HCl. |
priorityDate | 1969-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 122.