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filingDate 1989-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6c63b81a5d2de1cfe6e95f73ae98b51
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publicationDate 1990-09-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02223587-A
titleOfInvention Carbapenem derivative
abstract NEW MATERIAL:The compound of formula I [R 1 is H, (protected) hydroxy-lower alkyl, etc.; COOR 2 is (protected) carboxyl, etc.; R 3 is lower alkyl; R 4 is group of formula II (the group of formula III constituting the partial structure of R 4 is 5-membered or 6-membered nitrogen-containing heterocyclic group containing 1-4 hetero atoms selected from O, S and N; R 5 is H, nitro, etc.)]. n EXAMPLE: (1R,5S,6S,8R)-2-[(6,7-dihydro-5H-pyrrolo-[1, 2-C]imidazol-7-yl)thio]-6-(1- hydroxyethyl)-1-methyl-1-carbapen-2-em-3-carboxylic acid. n USE: Antibacterial agent against bacteria resistant to cephalosporin or penicillin, Gram-positive bacteria and Gram-negative bacteria. n PREPARATION: The objective compound of formula I is produced by oxidizing a compound of formula IV (R 2 is ester residue; R 7 is methyl, etc.) with peracetic acid, etc., in a solvent, substituting the resultant compound of formula V with a thiol compound of formula VI in methanol, etc., and, as necessary, deprotecting the product. n COPYRIGHT: (C)1990,JPO&Japio
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priorityDate 1988-11-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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