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filingDate 1995-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_486995bab6e66bcc721d164ff5808e2e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac828a0314c170f4b167636fce4b62d2
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publicationDate 1996-09-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H08245635-A
titleOfInvention Method for producing 2-isosephem derivative
abstract (57) [Summary] (Modified) [Objective] To provide a novel method for producing a cephem derivative which synthesizes a 3-halomethyl-2-isocephem derivative or a 3-halomethyl-2-oxaisosephem derivative in one step. [Structure] 2-azetidinyl-represented by the general formula (1) A compound represented by the general formula (2), which comprises reacting a 3,4-dihalogeno-2-butenoic acid compound with a thioacetic acid derivative which itself is basic or a mixture of a base and a thioacetic acid derivative in a water-containing organic solvent. Method for producing 3-halomethyl-2-isocephem derivative, and said 2-azetidinyl- A compound represented by the formula (3), which comprises reacting a 3,4-dihalogeno-2-butenoic acid compound with a base in a water-containing organic solvent. A method for producing a 3-halomethyl-2-oxaisocephem derivative represented by: [Wherein R 1 is a hydrogen atom or a (protected) amino group; R 2 is a hydrogen atom or a lower alkoxy group; R 3 is a hydrogen atom or a carboxylic acid protecting group; W is a leaving group; X, Y Are halogen atoms; ]
priorityDate 1995-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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