SYNTHESIS OF DESGLYMIDODRINE FROM MIDODRINE BY CONVENTIONAL AMIDE HYDROLYSIS METHOD

Authors

  • S. T. Narenderan Department of Pharmaceutical Analysis ,JSS College of Pharmacy, Ootacamund, Jagadguru Sri Shivarathreeshwara University, Mysore-643001, India
  • Srikanth Jupudi Department of Pharmaceutical Chemistry, JSS College of Pharmacy, Ootacamund, Jagadguru Sri Shivarathreeshwara University, Mysore-643001, India
  • P. Vanaja Department of Pharmaceutical Chemistry, JSS College of Pharmacy, Ootacamund, Jagadguru Sri Shivarathreeshwara University, Mysore-643001, India
  • S. N. Meyyanathan Department of Pharmaceutical Analysis ,JSS College of Pharmacy, Ootacamund, Jagadguru Sri Shivarathreeshwara University, Mysore-643001, India

DOI:

https://doi.org/10.22159/ijpps.2018v10i2.23251

Keywords:

Midodrine, Desglymidodrine, Amide hydrolysis

Abstract

Objective:  The term prodrug involves chemically modifying inert compound which upon administration releases the active parent drug to elicit its pharmacological response within the body. Acting as a α-adrenergic agonist, desglymidodrine an active metabolite of amide prodrug midodrine is used for the treatment of essential and orthostatic hypotension. In the present study synthesis of desglymidodrine from midodrine was reported.

Methods:  The synthesis was done by the conventional amide hydrolysis method.

Results:  A novel synthesis of desglymidodrine was successfully achieved and spectrally elucidated by infrared spectroscopy (IR), 1H, 13C nuclear magnetic resonance (NMR) and mass analysis.

Conclusion:  The acquired results were found to be accurate, the synthetic route appeared to be simple, cost-effective and time efficient. Hence the synthesized desglymidodrine can be as a reference standard for the estimation of the same.

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References

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Published

01-02-2018

How to Cite

Narenderan, S. T., S. Jupudi, P. Vanaja, and S. N. Meyyanathan. “SYNTHESIS OF DESGLYMIDODRINE FROM MIDODRINE BY CONVENTIONAL AMIDE HYDROLYSIS METHOD”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 10, no. 2, Feb. 2018, pp. 168-70, doi:10.22159/ijpps.2018v10i2.23251.

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Section

Short Communication(s)