Abstract An efficient process for the synthesis of API Fingolimod Hydrochloride is presented. This proposed synthesis involves simple commercially available octanophenone as a starting material. The route is effective involving seven steps to achieve the target, thus reducing the cycle time, and is cost efficient by 50%. It is an immune modulating drug for the treatment of heart failure and arrhythmias. Graphical Abstract

中文翻译：

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一种合成盐酸芬戈莫德的有效方法

摘要 提出了一种合成API 芬戈莫德盐酸盐的有效方法。该提议的合成涉及简单的市售辛苯酮作为起始材料。该路线是有效的，包括七个步骤来实现目标，从而减少周期时间，成本效率降低 50%。它是一种免疫调节药物，用于治疗心力衰竭和心律失常。图形概要