发明名称 NOVEL SYNTHESIS PROCESS FOR IVABRADINE AND ADDITION SALT THEREOF WITH PHARMACEUTICALLY ACCEPTABLE ACID
摘要 PROBLEM TO BE SOLVED: To provide a synthetic route for ivabradine in a high yield, which can eliminate the use of a hydride donor such as borohydride or noble metals such as a palladium catalyst, and which is useful in treatment and prevention of various kinds of clinical conditions of myocardial ischemia such as angina, myocardial infarction and rhythm disturbance associated with them, in various clinical conditions including the rhythm disturbance, particularly, supraventricular rhythm disturbance, and further in cardiac failure.SOLUTION: There are provided a process for synthesizing ivabradine represented by formula (I), an addition salt thereof with pharmaceutically acceptable acid, and a hydrate thereof.
申请公布号 JP2013129656(A) 申请公布日期 2013.07.04
申请号 JP20120276524 申请日期 2012.12.19
申请人 LAB SERVIER 发明人 RENAUD JEAN-LUC;PANNETIER NICOLAS;GAILLARD SYLVAIN;LECOUVE JEAN-PIERRE;VAYSSE-LUDOT LUCILE
分类号 C07D223/16;A61K31/55;A61P9/10 主分类号 C07D223/16
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