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filingDate 1981-12-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a7ec5b6bf4026515a1bdf5afab04cd15
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publicationDate 1982-07-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S57118560-A
titleOfInvention Preparation of 1-sulfo-2-oxoazetidine and its intermediate
abstract NEW MATERIAL:A compound shown by the formulaI(R 1 is amino which may be acylated or protected; X is H or methoxy). n EXAMPLE: Sodium 3-benzyloxycaboxamide-2-oxoazetidine-1-sulfonate. n USE: Having antimicrobial action or β-lactamase inhibiting action, useful for remedying or preventing infectious diseass of man and animals by use of it alone or it together with a β-lactam type antibiotic. n PROCESS: A compound shown by the formula II (R 2 is amino which may be acylated or protected) is reacted with a t-butyl or isopropylsilyl compound to give a t-butyl or isopropylsilyl derivative, which is sulfonated with sulfuric anhydride or its reactive derivative, and, if necessary, the protecting group is removed, to give a compound shown by the formulaI. n COPYRIGHT: (C)1982,JPO&Japio
priorityDate 1980-12-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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