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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83478Generated: October 27, 2026

Methanesulfonic Acid → Safinamide Mesylate

https://huagongshe.com/reaction/83478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantSafinamideHCID 131682—
SolventEthyl AcetateHCID 8857—
ProductSafinamide MesylateHCID 303850296.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (S)-2[4-(3-fluorobenzyloxy)benzylamino]propanamide (1.50 g, 4.96 mmol) and ethyl acetate (40.2 mL) is heated to 50° C. until a clear solution is obtained. Methanesulfonic acid (0.53 g, 5.51 mmol) is added under stirring in 15 min to the solution and the resulting heterogeneous mixture is cooled under stirring to 20° C. in 90 min. After 30 min at 20° C. the solid is collected by filtration, washed with ethyl acetate (6 mL) and dried at 50° C. at reduced pressure for 15 hrs to provide (S)-2[4-(3-fluorobenzyloxy)benzylamino]propanamide methanesulfonate (Ic) as a white solid in a 96.1% yield. The product has HPLC purity 98.6 (area %, see Example 25A) and a content of (S)-2-[3-(3-fluorobenzyl)-4-(3-fluorobenzyloxy)-benzylamino]propanamide methanesulfonate (IIc) of 0.10% by weight determined by HPLC (see Example 25B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846763B2
Source datasetuspto-grants-2014_09
ORD IDord-4deebfbb2d994f05a4209e0f55ba03de
Source noteuspto-grants-2014_09