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filingDate 1994-08-02^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e1b13399148ff2dc65faef6c81a5179a
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_77c4f8ece7377ecb33d61221e930c4ca
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f5759e7e977274db2107f6915e07432e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57a3be057e3880135540e84a15ba1753
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfa423cedaa788099e726079b1d8ea39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea6d04c4c62436f67bc65fa3f3c23b01
publicationDate 1995-02-04^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2129301-A1
titleOfInvention Benzo-fused heterocyclic compounds with a 5-membered ring, process for their preparation, their use as medicaments, their use as diagnostic agents, and medicaments containing them
abstract HOECHST AKTIENGESELLSCHAFT - HOE 93/F 223 K Dr.VF/we Abstract Benzo-fused heterocyclic compounds having a 5-membered ring, processes for their preparation, their use as medicaments, their use as diagnostic agents and medica-ments containing them Benzo-fused heterocyclic compounds having a 5-membered ring, of the formula I (I) where X is N or CR(6); Y is oxygen, S or NR(7); A and B together are a bond or are both hydrogen, if, at the same time, X is CR(6) and Y is NR(7), one of the substituents R(1) to R(6) is a -CO-N=C(NR2)2 group; the other respective substituents R(1) to R(6) are H, Hal or alkyl; up to two of the other substituents R(1) to R(6) are CN, N02, N3, (C1-C4)-alkoxy, CF3; up to one of the other substituents is R(8)-CnH2n-Z- or phenyl; R(7) is H, alk(en)yl or R(8)-CnH2n-, and pharmaceutically tolerated salts thereof, are described. A process for the preparation of the compounds I which comprises reacting a compound of the formula II (II) in which one of the substituents R(1)' to R(5)' is a -CO-L group and L is a leaving group which can easily be replaced nucleophilically, with guanidine, and, if appropriate, converting the product into the pharmaco-logically tolerated salt, furthermore is also described.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9394285-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-8889730-B2
priorityDate 1993-08-03^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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