发明名称 New method for synthesising ivabradine and its added salts with a pharmaceutically acceptable acid.
摘要 <p>Preparing (P1) ivabradine (I) involves reductive amination reaction of 4-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-butyraldehyde (V) with ((S)-3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-methyl-amine (VI) in the presence of an iron-based catalyst, optionally in the presence of trimethylamine N-oxide, under dihydrogen pressure of 1-20 bars, in an organic solvent or mixture of organic solvents, at 25-100[deg] C. ACTIVITY : Cardiant; Vasotropic; Antianginal. No biological data given. MECHANISM OF ACTION : None given.</p>
申请公布号 SI2607353(T1) 申请公布日期 2014.12.31
申请号 SI20120030089T 申请日期 2012.11.09
申请人 LES LABORATOIRES SERVIER 发明人 RENAUD JEAN-LUC;PANNETIER NICOLAS;LECOUVE JEAN-PIERRE;VAYSSE-LUDOT LUCILE;MOULIN SOLENNE
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