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

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