http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1298157-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_dc2e3d9792e0546ce6a766cc0e439b28
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D333-68
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D333-68
filingDate 1970-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1972-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1298157-A
titleOfInvention BENZO-(b)-THIOPHENE DERIVATIVES AND COMPOSITIONS CONTAINING THE SAME
abstract 1298157 Benzo(b)thiophene derivatives CENTRE D'ETUDES POUR L'INDUSTRIE PHARMACEUTIQUE 6 March 1970 [7 March 1969] 10973/70 Heading C2C Novel benzo(b)thiophene derivatives of the formula wherein A is C 1-6 alkylene; and R and R<SP>1</SP>, which may be the same or different, each are H, or optionally substituted alkyl, cycloalkyl or aralkyl, or R and R<SP>1</SP> together with the nitrogen atom to which they are attached form a 5-7. membered saturated heterocyclic ring, optionally containing further hetero atoms, and/or opt - ionally substituted by one or more C 1-4 alkyl or C 1-4 hydroxyalkyl groups; and acid addition and quaternary ammonium salts thereof, are prepared by reacting the appropriate 3-carbamoyl - 2 - haloacylamino - 4,5,6,7 - tetrahydrobenzo(b)thiophenes with compounds of the formula 2 - (Chloroacetylamino)- 3 - carbamoyl - 4,5,6, 7 - tetrahydrobenzo(b)thiophene and 2 - (3- bromopropionylamino)- 3 - carbamoyl - 4,5,6,7- tetrahydrobenzo(b)thiophene are obtained by reacting 2 - amino - 3 - carbamoyl - 4,5,6,7 - tetrahydrobenzo(b)thiophene with chloroacetyl chloride and 3-bromopropionyl bromide respectively. Pharmaceutical compositions, suitable for oral, parenteral, rectal or topical administration, contain the above novel compounds or physiologically acceptable acid addition or quaternary ammonium salts thereof, in association with pharmaceutical carriers and/or excipients. The compositions have anti-arrhythmic, anti-histaminic, anti-tussive and anti-inflammatory activities and may also be used as local anaesthetics.
priorityDate 1969-03-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 21.