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filingDate 2011-09-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2747444c91410731c6881f97efbbcd3d
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publicationDate 2011-12-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2011319666-A1
titleOfInvention Method of obtaining 3,3-diphenylpropylamines
abstract The invention relates to a method of obtaining 3,3-diphenylpropylamines (I), wherein R 1 is H, alkyl, haloalkyl or alkoxyalkyl, R 2 is alkyl, alkoxy, halogen, NO 2 , CN, CHO, which may be free or protected, CH 2 OH or COOR 6 , and R 2 and R 1 are selected independently from H and alkyl or together with the nitrogen to which they are bound form a ring having 3 to 7 members. The inventive method consists in reacting a propylenephenylamine and a disubstituted aromatic hydrocarbon and, if necessary, separating the desired enantiomer or the mixture of enantiomers, and/or converting the compound (I) into a salt. Compounds (I) are muscarinic receptor antagonists which can be used in the treatment of urinary incontinence and other symptoms of urinary bladder hyperactivity. Said compounds include tolterodine.
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