http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1274832-A

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filingDate 1986-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1990-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18bfa02ba18524fe03d67758229567e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_962d36b78abebd78e303ae41b72e2583
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1558be2eff4b658f2e88c8d2a8210663
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b24e3bd9971dcbefa97cdb8e9e7db88c
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publicationDate 1990-10-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1274832-A
titleOfInvention 7-substituted bicyclic pyrazolidinones
abstract ABSTRACT OF THE DISCLOSURE The invention disclosed herein provides 7-substituted bicyclic pyrazolidinone compounds of the formula: I one of R1 and R2 is hydrogen, halo, C1 to C6 alkyl, C1 to C6 substituted alkyl, perfluoro C2 to C4 alkyl, C7 to C12 arylalkyl, C7 to C12 substituted aryl-alkyl, phenyl, substituted phenyl, a heterocyclic ring, nitro or cyano; a group of the formula wherein X is fluoro, chloro, bromo or iodo; a group of the formula wherein z is 0, 1 or 2 and R7 is C1 to C6 alkyl, C1 to C6 substituted alkyl, phenyl, substituted phenyl, C7 to C12 arylalkyl, C7 to C12 substituted aryl-alkyl or a heterocyclic ring; a group of the formula wherein R8 is hydrogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, perfluoro C2 to C4 alkyl, trihalomethyl, C7 to C12 arylalkyl, C7 to C12 substituted aryl-alkyl, phenyl, substituted phenyl, amino, (monosubstituted)amino or (disubstituted)-amino; a group of the formula wherein R9 is hydrogen, an organic or inorganic cation, C1 to C6 alkyl, C1 to C6 substituted alkyl, C7 to C12 aryl-alkyl, C7 to C12 substituted arylalkyl, phenyl, substituted phenyl, a carboxy-protecting group or a non-toxic, metabolically-labile ester-forming group; a group of the formula PO3(R10)2 wherein R10 is hydrogen, an organic or inorganic cation, C1 to C6 alkyl, C1 to C6 substituted alkyl, C7 to C12 aryl-alkyl, C7 to C12 substituted arylalkyl, phenyl, or substituted phenyl; a group of the formula -CH2-??Q wherein -??Q is a quaternary ammonium group; or or a group of the formula -CH2-S-Heterocyclic ring; a group of the formula wherein R11 is hydrogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C7 to C12 arylalkyl, C7 to C12 substituted arylalkyl, phenyl, sub-stituted phenyl or C1 to C7 acyl; or a group of the formula wherein R12 and R13 are the same or different and are hydrogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C7 to C12 arylalkyl, C7 to C12 substituted arylalkyl, phenyl, substituted phenyl, C1 to C7 acyl, or a group of the formula; wherein Rq is C1 to C6 alkyl, C7 to C12 arylalkyl or phenyl; and the other of R1 and R2 is a group of the formula wherein R14 is hydrogen, an organic or inorganic cation, a carboxy-projecting group, or a non-toxic, metabolically-labile ester forming group; R3 and R4 are the same or different and are hydxogen, C1 to C6 alkyl, C1 to C6 substituted alkyl, C7 to C12 arylalkyl, C7 to C12 substituted arylalkyl, phenyl, substituted phenyl or a group of the formula wherein R15 has the same definition as R9; R5 and R6 are 1) each hydrogen, an amino protecting group or an acyl group derived from a C1 to C30 carboxylic acid; provided that at least one of R5 and R6 must be hydrogen; or 2) taken together to form a phthalimido group; or a pharmaceutically acceptable salt thereof. These compounds are antimicrobials, and are useful for treating bacterial infections.
priorityDate 1985-04-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 754.