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Research Article Open access CC BY 4.0

An Efficient Synthesis of 4-Aminomethyl-1-(2-Phenylethyl)-Piperidin-4-ol: A Key Intermediate in Fenspiride HCl Synthesis

Prasad Panchabhai, Neelakandan Kaliaperumal, Gopalakrishnan Mannathusamy, Anbuselvan Chinnadurai

Journal of Pharmaceutical Research International · pp. 139–146 · Published 25 Nov 2021

10.9734/jpri/2021/v33i51B33523

Abstract

The article confers a scalable manufacturing process of Fenspiride HCl. 4-aminomethyl-1-(2-phenylethyl)-piperidin-4-ol is the main building block in Fenspiride HCl synthesis. The reported reagents for 4-aminomethyl-1-(2-phenylethyl)-piperidin-4-ol synthesis are costly, explosive, highly toxic, produce hazardous waste, and also need to be handled with most care. The paper introduces aqueous ammonia as an alternate reagent in Fenspiride HCl and used in 4-aminomethyl-1-(2-phenylethyl)-piperidin-4-ol synthesis. The new green chemistry aspect makes the process environment-friendly and cheaper. It also eliminates toxic, sensitive, and hazardous reagents and makes the process safe on uncomplicated on bulk scale production. The high pure Fenspiride HCl is obtained by following this process and meets the ICH limits with good yield.

Antitussives endotoxamia treatment aq. ammonia fenspiride HCl commercial viable ICH limits active pharmaceutical ingredient

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