http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CH-629801-A5

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-38
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filingDate 1976-02-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9b640ca8edd44ae27ddd529a62847913
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_93e80e6f0184c5b7318a4254a225cc38
publicationDate 1982-05-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-629801-A5
titleOfInvention Process for the preparation of bispyrrolinyl derivatives of phenothiazines, phenoxazines and acridans
abstract Bispyrrolinyl derivatives of phenothiazines, phenoxazines and acridans are obtained by reacting a phenothiazine, phenoxazine or acridan with a pyrrolidinone in the presence of phosphorus oxychloride. The phenothiazine, phenoxazine or acridan can likewise be converted by alkylation with 2-chloro-1-(1-pyrrolin-2-yl)-2-pyrroline into the required compounds. Typical examples of these bispyrrolinyl derivatives are 2-methoxy-10-[5-methyl-1-(5-methyl-1-pyrrolin-2-yl)-2-pyrrolin-2-yl]-p henothiazine, 10-[1-(1-pyrrolin-2-yl)-2-pyrrolin-2-yl]phenoxazine and 9,9-dimethyl-10-[5-methyl-1-(5-methyl-1-pyrrolin-2-yl)-2-pyrrolin-2-yl ]acridan. The amidine compounds can be used as diuretics, smooth muscle relaxants and antithrombogenic agents.
priorityDate 1975-12-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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