http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63183525-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_59e1d955a7b1560dc68cf7fd800e8fac |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-165 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P9-06 |
filingDate | 1987-09-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a832195989f6b4367c3421dd61c43f83 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c4c704303231b550e09a11f46ce43ab7 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6b2e6c771d1b12e5a0803c90f0aa8757 |
publicationDate | 1988-07-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-S63183525-A |
titleOfInvention | Remedy for arrhythmia |
abstract | NEW MATERIAL:A compound shown by formula I (R 1 and R 2 are 1W3C alkyl; R 3 is H or 1W3C alkyl; R 4 and R 5 are H or 1W8C alkyl; m and n are 1W7; with the proviso that R 4 and R 5 are not H at the same time) and a salt thereof. n EXAMPLE: 3-(Diisopropylaminoethylamino)-2',6'-dimethylpropionanilide. n USE: A remedy for arrhythmia having prolonged effects for a long time by oral administration, no anti-choline action, no central inhibitory action and no blood sugar lowering action which is unsuitable for treating arrhythmia. n PREPARATION: A chloroalkylanilide derivative shown by formula II is reacted with a diamine derivative shown by formula III in a toluene solution of triethylamine by heating under reflux to give a compound shown by formula I. n COPYRIGHT: (C)1988,JPO&Japio |
priorityDate | 1986-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 22.