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filingDate 1987-11-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_871eecf9ab65f9585702f44953882379
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publicationDate 1988-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0269968-A2
titleOfInvention Heteroaromatic amine derivatives, medicaments containing them and process for their preparation
abstract The present invention relates to new heteroaromatic amine derivatives of the general formula in the n is the number 0 or 1, A is a methylene, carbonyl or thiocarbonyl group, B is a methylene, carbonyl or thiocarbonyl group, where only one of the radicals A or B can be a thiocarbonyl group and in this case the other of the radicals A or B must be a methylene group, E is a straight-chain alkylene group optionally substituted by an alkyl group, G is a straight-chain alkylene group optionally substituted by an alkyl group, R₁ and R₂, which may be the same or different, are hydrogen atoms, alkyl or alkoxy groups or R₁ and R₂ together are an alkylenedioxy group, R₃ is a hydrogen atom, an alkenyl group, an alkyl or phenylalkyl group and Het has a 5- or 6-membered heteroaromatic ring which is bonded via a carbon or nitrogen atom and which contains one oxygen, sulfur or nitrogen atom, two nitrogen atoms or one nitrogen atom and one oxygen or sulfur atom, to which a 1 is additionally attached via two adjacent carbon atoms , 3-propylene, 1,4-butylene or 1,4-buta-1,3-dienylene group can be bonded, in which case the bond can also take place via the carbon ring, and in which the carbon skeleton of the aromatic mentioned above and heteroaromatic rings through a halogen atom, an alkyl, hydroxy, alkoxy, phenylalkoxy, phenyl, dimethoxyphenyl, nitro, amino, acetylamino, carbamoylamino, N-alkyl-carbamoylamino, hydroxymethyl, mercapto , Alkylmercapto, alkylsulfinyl, alkylsulfonyl, alkylsulfonyloxy, alkylsulfonylamino, alkoxycarbonylmethoxy, carboxymethoxy or alkoxymethyl group mono- or disubstituted or by a methylenedioxy or ethylenedi oxy group can be substituted and at the same time an optionally present imino group in the heteroaromatic radicals mentioned above can be substituted by an alkyl, phenylalkyl or phenyl group, mean their N-oxides, their enantiomers, their diastereomers and their acid addition salts with inorganic or organic acids, which have valuable pharmacological properties, in particular a heart rate lowering and a positive inotropic effect.n n n The new compounds can be prepared by processes known per se.
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http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235008283
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897689
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897686
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235008276
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897687
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235008268
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24905
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409982724
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235008274
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897685
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID421662834
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897682
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID12748
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1140
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127971973
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897683
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128576874
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19897680
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454463664
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3826198
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID235008260

Total number of triples: 926.