HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → Lacosamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (R)-2-Amino-N-benzyl-3-methoxypropionamide | HCID 10104501 | — |
| Product | Lacosamide | HCID 219078 | — |
Reaction Steps
The (R)-2-amino-N-benzyl-3-methoxypropionamide solution prepared above was cooled to <5° C. and acetic anhydride (10 ml, 0.106 mol) added at <15° C. The reaction mixture is warmed to room temperature over 30 minutes and aged for a further 30 minutes. The mixture is then washed with water (44 ml), 8% sodium bicarbonate (44 ml) and water (44 ml). The methylene chloride was exchanged for ethyl acetate by distillation and the solution distilled to a volume of 115 ml. The product was crystallised by cooling the solution to 0-5° C. and the pure Lacosamide isolated by filtration (18.7 g, 69.8%) HPLC purity 99.98%, Chiral purity 99.8% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08809585B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-bcd706ee98ee478aa60cc25ea5ac4654 |
| Source note | uspto-grants-2014_08 |