http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H05202003-A

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filingDate 1991-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_412d2ca0770cf07daef50d9292ad197d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_303af36115a2f1c7e800e94ca70ada6e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_776e6d78c07a7e9fb4150276ebd639bf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_145d61eb5cf6c913ca1d9c30929aec42
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00bcc8a8df41a6a5418cae37d57c5cfb
publicationDate 1993-08-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H05202003-A
titleOfInvention Novel sulfonamides as antibacterial agents
abstract (57) [Summary] (Modified) [Objective] To provide sulfonamides having antifungal activity. A compound of formula I, a compound of general Ia in which it is cyclized to isooxozolidine, and pharmaceutically acceptable salts thereof, a process for their preparation, and pharmaceutical and agrochemical compositions containing the above compounds object [Wherein X is N, CH; R 1 is C 1-6 alkyl, 1, 2,4-triazol-1-yl-C 1-6 alkyl, Phenyl -C 1-4 alkyl or the like; R 2 is H, C 1-6 alkyl, phenyl -C 1-4 alkyl, Ikowa (pyridyl, furyl, Choi two Lucia benzisoxazolyl) -C 1-4 alkyl such as; R 3 is hydrogen; R 4 is hydrogen or (1H-1,2,4- Triazol-1-ylmethyl); R 5 is hydrogen, C 1-6 alkyl, (substituted) phenyl; R 7 is hydrogen, C 1-6 alkyl; Ar is (one or more halo, CF3 substituted) Phenyl group]
priorityDate 1990-10-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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