The title compound is isolated in pure form by using a crystallization process and converted to its pharmaceutically acceptable salts. The crystallization process affects stability and purity of the amlodipine salts. All known impurities and one unknown impurity, which forms during the synthesis of the amlodipine salts, were isolated, characterized, and synthesized. A new method allowing the quantitative HPLC analysis of all related impurities of amlodipine salts in a single chromatogram was developed.
该化合物的标题化合物通过结晶过程纯化并转化为其药用可接受的盐。结晶过程影响
氨氯地平盐的稳定性和纯度。所有已知杂质和在
氨氯地平盐合成过程中形成的一种未知杂质均被分离、表征和合成。开发了一种新方法,允许在单个色谱图中定量HPLC分析
氨氯地平盐的所有相关杂质。