Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(2-Oxopyrrolidin-1-yl)butanoic acid, (2R)- | HCID 11600747 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Etiracetam, (R)- | HCID 441341 | 80.8% |
Reaction Steps
A suspension of (R)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (35 g, 0.20 mol) in methylene chloride (225 ml) was cooled to 0° C. and triethylamine (41 g, 0.40 mol) and methanesulfonyl chloride (29 g, 0.26 mol) were added dropwise. The mixture was stirred at 0° C. for 30 min., then a stream of ammonia was purged in the solution at 0° C. for 2 hours. The insoluble solids were filtered and the filtrate was concentrated. The product was recrystallized from methyl isobutyl ketone to give 27.5 g (78%) of (R)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902380B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-fe3d671ac3dd48b7a8e1e125bcf09ad2 |
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| Source note | uspto-grants-2011_03 |
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