GET THE APP

A new process for the synthesis of enantiomerically pure R-(+)-Npropargyl-1-aminoindan mesylate(Rasagiline mesylate) | Abstract

Der Pharma Chemica
Journal for Medicinal Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences and Computational Chemistry

ISSN: 0975-413X
All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission Systemof respective journal.

Abstract

A new process for the synthesis of enantiomerically pure R-(+)-Npropargyl-1-aminoindan mesylate(Rasagiline mesylate)

Author(s): K. Tatendra Reddy, K. Suneel Kumar, G. Omprakash, P. K. Dubey,

A new processdeveloped for the synthesis of enantiomerically pure R-(+)-N-propargyl-1- aminoindan mesylate(Rasagiline mesylate) by using K2HPO4/Triethylbenzylammonium chloride (TEBAC) as a reagent. This approach controls the formation of other isomerS-(-)-N-propargyl- 1-aminoindane. This new process may be useful for the preparation of enantiomerically pure Rasagiline mesylatein commercial scale with good yields.


PDF

Select your language of interest to view the total content in your interested language

30+ Million Readerbase
SCImago Journal & Country Rank
Google Scholar citation report
Citations : 25868

Der Pharma Chemica received 25868 citations as per Google Scholar report

Der Pharma Chemica peer review process verified at publons
Der Pharma Chemica- Journals on pharmaceutical chemistry