发明名称 Process for the synthesis of ivabradine and its pharmaceutically acceptable acid addition salts
摘要 Preparing tetrahydro-benzo[d]azepin-2-one compounds (A) comprises: reacting 3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-propionitrile (VIII) with (3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-methyl-amine (IXa) in the presence of e.g. lanthanide in a solvent to obtain N-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-N-methyl-propionamidine (Xa) in its racemic or optically active form; and transforming (Xa) by the action of a hydride donor. Preparing tetrahydro-benzo[d]azepin-2-one compounds (A) comprising 3-{3-[(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-methyl-amino]-propyl}-7,8-dimethoxy-1,3,4,5-tetrahydro-benzo[d]azepin-2-one (ivabradine) (I) and 3-{3-[(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-amino]-propyl}-7,8-dimethoxy-1,3,4,5-tetrahydro-benzo[d]azepin-2-one (II) in their racemic or optically active form comprises: reacting 3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-propionitrile (VIII) with (3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-methyl-amine (IXa) or C-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-yl)-methylamine (IXb) in the presence of transition metal or lanthanide in a solvent to obtain N-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-N-methyl-propionamidine (Xa) or N-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-propionamidine (Xb) in its racemic or optically active form; and transforming (Xa) or (Xb) by the action of a hydride donor. Independent claims are included for: (1) 3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-propionitrile (VIII); (2) N-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-N-methyl-propionamidine (Xa); and (3) N-(3,4-dimethoxy-bicyclo[4.2.0]octa-1(6),2,4-trien-7-ylmethyl)-3-(7,8-dimethoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d]azepin-3-yl)-propionamidine (Xb). ACTIVITY : Cardiant; Vasotropic; Antianginal; Antiarrhythmic. MECHANISM OF ACTION : None given.
申请公布号 PL2241554(T3) 申请公布日期 2012.01.31
申请号 PL10290166T 申请日期 2010.03.30
申请人 发明人 PEGLION JEAN-LOUIS;DESSINGES AIMEE;SERKIZ BERNARD
分类号 C07D223/16 主分类号 C07D223/16
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