Abstract

BackgroundSildenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specifil phophodiesterase type 5 (PDE5). Sildenafil enhances the effect of nitric oxide by inhibiting phosphodiesterase type 5, which is responsible for the degradation of cGMP in the corpus cavernosum. The possible genotoxic impurities of sildenafil were synthesized, i.e., sildenafil sulfonyl methyl ester, sildenafil sulfonyl ethyl ester, and sildenafil sulfonyl isopropyl ester. The present work describes the synthesis and characterization of these sulfonyl ester compounds related to sildenafil.ResultsAll the synthesized sildenafil sulfonyl esters have proved to be beneficial for the pharmaceutical industry in view of the regulatory importance.ConclusionA simple, efficient, and repeatable method was developed for the preparation of sildenafil sulfonyl esters in view of the regulatory importance of the potential genotoxic impurities in the active pharmaceutical ingredient. A detailed study of various impurities in sildenafil was conducted. Different process-related sulfonyl esters in sildenafil were identified, synthesized, and characterized by using various spectroscopic techniques like liquid chromatography-mass spectrometry (LCMS), mass, 1H NMR, and FT-IR. These efforts to synthesize and characterize them effectively have proved to be beneficial.

Highlights

  • Sildenafil is a selective inhibitor of cyclic guanosine monophosphate-specifil phophodiesterase type 5 (PDE5)

  • Sildenafil is used for the treatment of erectile dysfunction in male and it is used for hypertension, and its citrate salt 1 is marketed by Pfizer under the brand names Viagra® and Revatio®

  • Sildenafil citrate 1 has been synthesized by known literature methods [6,7,8]

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Summary

Introduction

Sildenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specifil phophodiesterase type 5 (PDE5). Sildenafil enhances the effect of nitric oxide by inhibiting phosphodiesterase type 5, which is responsible for the degradation of cGMP in the corpus cavernosum. The possible genotoxic impurities of sildenafil were synthesized, i.e., sildenafil sulfonyl methyl ester, sildenafil sulfonyl ethyl ester, and sildenafil sulfonyl isopropyl ester. The present work describes the synthesis and characterization of these sulfonyl ester compounds related to sildenafil. Impurities present in an active pharmaceutical ingredient (API) will influence drug effectiveness by the change of quality and safety. In view of the regulatory importance of the genotoxic impurities [3,4,5] in the API, a detailed assessment study. Rajesh Reddy et al Future Journal of Pharmaceutical Sciences (2020) 6:83 on potential genotoxic impurities in sildenafil was conducted. The genotoxic structure evolution was further confirmed by Derek and Sarah analysis

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