http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1281321-C

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filingDate 1985-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b6f2a1c1d2caff6261f52b4409a85ef1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c03f8032cc75702440cb4353e18ed51e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e569b72ea9b3cdf25357ae54d58733da
publicationDate 1991-03-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1281321-C
titleOfInvention Spasmolytically active tertiary amine derivatives and method of preparing the same
abstract ABSTRACT New spasmolytic active tertiary amine derivatives, salts thereof, and processes for their preparation, of the formula 1 are described 1 in which the groups R represent a range of possibilities, typically hydrogen or an alkyl or alkylene group; A is a phenyl or heteroaryl group having 5 or 6 members; Z is the group NR12 or an oxygen atom, R12 being hydrogen or alkyl; n is zero or 1; and X is a carbonyl, thiocarbonyl or SO2 group. In the compounds wherein R4 is other than hydrogen, the S-configuration of the chiral center is pre-ferred. A typical compound is These compounds do not exhibit the peripheral and central muscarino-lytic side effects characteristic of other neurotropic spasmolytics, for example atropine and secorerine.
priorityDate 1984-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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