HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Rasagiline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Propyn-1-ol, 1-benzenesulfonate | HCID 80273 | — |
| Reactant | (+-)-1-Aminoindan | HCID 123445 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Rasagiline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741962B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-0bba4b190b374546a4df81e5fdfebfb8 |
| Source note | uspto-grants-2014_06 |