Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from FR0403830Aexternal-prioritypatent/FR2868777B1/en
Application filed by Servier LabfiledCriticalServier Lab
Priority to TNP2005000049ApriorityCriticalpatent/TNSN05049A1/en
Publication of TNSN05049A1publicationCriticalpatent/TNSN05049A1/en
Pharmaceuticals Containing Other Organic And Inorganic Compounds
(AREA)
Saccharide Compounds
(AREA)
Abstract
PROCEDE DE SYNTHESE DE L'IVABRADINE DE FORMULE (1) : DE SES SELS D'ADDITION A UN ACIDE PHARMACEUTIQUEMENT ACCEPTABLE ET DE SES HYDRATES; FORME CRISTALLINE (ALPHA) DU CHLORHYDRATE DE L'IVABRADINE. MEDICAMENTS.A METHOD OF SYNTHESIZING IVABRADIN OF FORMULA (1): ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID AND ITS HYDRATES; CRYSTALLINE FORM (ALPHA) OF IVABRADINE HYDROCHLORIDE. DRUGS.
TNP2005000049A2004-04-132005-02-18
NOVEL PROCESS FOR THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID
TNSN05049A1
(en)
NEW PROCESS FOR THE SYNTHESIS OF (1S) -4,5-DIMETHOXY-1- (METHYLAMINOMETHYL) -BENZOCYCLOBUTANE AND ITS ADDITIONAL SALTS, AND APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS ADDITIONAL SALTS TO A PHARMACEUTICAL ACID ACCEPTABLE
NOVEL PROCESS FOR THE SYNTHESIS OF 7,8-DIMETHOXY-1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE AND THE APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID
NOVEL PROCESS FOR THE PREPARATION OF FUNCTIONALIZED BENZOCYCLOBUTENES, AND APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID
NOVEL PROCESS FOR THE SYNTHESIS OF 1,3,4,5-TETRAHYDRO-2H-3-BENZAZEPIN-2-ONE DERIVATIVES AND THE APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID
NOVEL PROCESS FOR THE SYNTHESIS OF 1,3-DIHYDRO-2H-3-BENZAZEPIN-2-ONE DERIVATIVES AND THE APPLICATION TO THE SYNTHESIS OF IVABRADINE AND ITS SALTS OF ADDITION TO A PHARMACEUTICALLY ACCEPTABLE ACID