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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061154Generated: October 27, 2026

Methanesulfonic Acid → Safinamide Mesylate

https://huagongshe.com/reaction/2061154

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 minutes to the solution and the resulting heterogeneous mixture is cooled under stirring to 20° C. in 90 minutes. After 30 minutes 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 17A) 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 17B).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278485B2
Source datasetuspto-grants-2012_10
ORD IDord-54d14dd4e7c54686ace587cfbf1115c8
Source noteuspto-grants-2012_10