http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CS-271489-B2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0d269c8e41f178194d858c230c9f85e3 |
| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-56 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-64 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D215-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-66 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-14 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-82 |
| filingDate | 1988-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_49eed030b65e409411b6d90adb66aa1e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_85c971f03b0244fb6913f07e03e6d35a http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_07d6e3a93748a6f0672a683e3e16f27c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_317f91390866e288684c92a254b16827 |
| publicationDate | 1990-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CS-271489-B2 |
| titleOfInvention | Method of alkylsulphonamidophenethylamines' sulphonamidoderivatives production |
| abstract | The method of production of sulfonamide derivates of alkyl sulfonamide phenethylamines is of a general formula I, where alk is C1-4-alkyl, R<1> is C1-4-alkyl and Het is the rest of the formula E, F or G, in which R<2> is hydrogen, methyl or ethyl, X is oxygen, sulphur or the rest of NR<4>, where R<4> is hydrogen or methyl and their pharmaceutically utilizable salts, characteristic by the fact that a compound of the general formula B, where R<a> is an amino group or the rest NHSO2alk and Het is the rest of the formula E, F or G; which can instead of -NHSO2alk configuration contain also an amino group providing that in the starting substance molecule there is at least one amino group is let to react with the C1-4-alkansulfonylchloride or -bromide or with an anhydride of C1-4-alkan-sulphonic acid. Finally the product of the general formula I is converted to salt. The produced compounds are efficient as anti-arrhythmic active substances and can be used in pharmaceuticals.<IMAGE> |
| priorityDate | 1988-05-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 144.