HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83478Generated: October 27, 2026
Methanesulfonic Acid → Safinamide Mesylate
https://huagongshe.com/reaction/83478
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Safinamide | HCID 131682 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Safinamide Mesylate | HCID 3038502 | 96.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846763B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-4deebfbb2d994f05a4209e0f55ba03de |
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| Source note | uspto-grants-2014_09 |
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