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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401852Generated: October 30, 2026

Sodium Hydroxide → Rasagiline

https://huagongshe.com/reaction/401852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2-Propyn-1-ol, 1-benzenesulfonateHCID 80273—
Reactant(+-)-1-AminoindanHCID 123445—
SolventTolueneHCID 1140—
ProductRasagilineHCID 3052776—

Reaction Steps

U.S. Pat. No. 5,532,415 discloses process for preparation of R(+)-Rasagiline mesylate which comprises treating a solution of propargyl benzenesulfonate (3) and racemic aminoindan (2) in toluene with aqueous solution of 15% sodium hydroxide to get racemic Rasagiline base (4). The obtained crude racemic Rasagiline is treated with L-tartaric acid in isopropanol (IPA) to get di(R-(+)-N-propargyl-1-aminoindan)-L-tartrate (5) which is recrystallized from 1:1 methanol/isopropanol. The obtained tartrate salt is reacted with methanesulphonic acid in isopropanol at reflux to obtain R(+)-Rasagiline mesylate. The disadvantage of this process is that the scheme consists of low atom efficiency and involves several steps to obtain the final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741962B2
Source datasetuspto-grants-2014_06
ORD IDord-0bba4b190b374546a4df81e5fdfebfb8
Source noteuspto-grants-2014_06