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filingDate 1978-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fdb37f8e92f27cfd3050285b2df430ae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4cc4f43c6b401398103ef01d9ce42a5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_94568d1b93f7f2c6ec1815fc8d9ce9e2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3dab800f033af36ed4d3bdfd6de150f8
publicationDate 1982-10-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SE-425486-B
titleOfInvention HETEROCYCLIC SUBSTITUTED BENZOIC ACID DERIVATIVES AS INTERMEDIATES FOR THE PREPARATION OF DIURETIC USEFUL HETEROCYCLIC SUBSTITUTED 5-SULFAMOYL BENZOIC ACID DERIVATIVE
abstract 1504505 Sulphonamides HOECHST AG 25 April 1975 [25 April 1974 27 Dec 1974] 17337/75 Heading C2C The invention comprises novel compounds (I) (including salts thereof) in which R1 and R2, which may be identical or different, each represents a hydrogen atom or an alkyl group having from 1 to 4 carbon atoms, and, if R1 represents a hydrogen atom, R2 may also represent an alkoxymethyl group having from 1 to 4 carbon atoms in the alkoxy radical, a phenoxymethyl group or a phenylthiomethyl group, R3 represents a hydrogen atom, a straight or branched chain alkyl group having from 1 to 4 carbon atoms, a cycloalkyl group, having 5 or 6 ring members, one of which may be replaced by an oxygen or sulphur atom, a phenyl or benzyl group which may be substituted in the phenyl nucleus by one or more substituents selected from nitro groups, alkyl groups having from 1 to 3 carbon atoms, alkoxy groups having from 1 to 5 carbon atoms and halogen atoms, or represents a benzhydryl group or an alkanoyloxymethyl group having 2 to 4 carbon atoms in the alkanoyl part, X represents a halogen atom, a CF 3 or CCl 3 group, a straight or branched chain, saturated or unsaturated alkyl group having from 1 to 6 carbon atoms, a benzyl group which may be substituted in the phenyl nucleus by one or more substituents selected from halogen atoms, hydroxy and amino groups, and alkyl and alkoxy groups, or represents one of the groups -O-R4, -S-R4, SO-R4, SO 2 -R4 and NR4R5, in which R4 represents a phenyl group which may be substituted by one or more substituents selected from halogen atoms, CF 3 , OH and amino groups, alkyl and alkoxy groups having from 1 to 4 carbon atoms, and SO 2 NH 2 groups, or represents a straight or branched chain alkyl group having from 1 to 4 carbon atoms which may be substituted by a phenyl, pyridyl, furyl or thienyl group, and R5 represents a hydrogen atom, a straight or branched chain alkyl group having from 1 to 4 carbon atoms, and the group NR4R5 may represent a saturated, heterocyclic, 5- or 6-membered ring which may be interrupted by an O-, N- or S- atom, A represents a single bond, or an alkylene chain of 1 to 3 carbon atoms which may be unsaturated, interrupted by O-, N- or S-atoms or substituted by halogen atoms and/or substituted by alkyl, aralkyl, aryl groups or by mono-nuclear hetero-aromatic rings, or A represents an ortho-phenylene radical or the grouping in which Y represents a single bond or an alkylene group having from 1 to 4 carbon atoms, and R6 and R7, which may be identical or different, each represents a hydrogen or halogen atom or an alkyl group having from 1 to 4 carbon atoms. They are made by standard methods. Pharmaceutical preparations having diuretic and saluretic action contain (I) as active ingredient. Administration is enterally or parenterally.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DK-156300-B
priorityDate 1974-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID432336003
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23694484
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21312195
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7940
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425193155
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54370826
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24638
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451071491
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54142238
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419541999
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID154290018
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419539539
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419522661
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID54334932
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394834
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID451228723
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3603687
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415815797
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70607453
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458394811
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID2849586
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87067
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21312113
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID450459896
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419521000
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419522973
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID90787550
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422549091
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID423459611
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4849
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153744332
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID422219388
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID21312199
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID424622782
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID153826905
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID13020993
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID465925671
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID11848
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID783

Total number of triples: 321.