Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 69491090 | HCID 69491090 | — |
| Product | HCID 9997536 | HCID 9997536 | — |
Reaction Steps
A solution of 250 mg (0.7 mmol) of (R)-3-amino-1-[4-(3-fluoro-benzyloxy)-phenyl]-pyrrolidin-2-one hydrochloride and 294 mg (2.2 mmol) of N-ethyl-diisopropylamine in 2 ml of N,N-dimethylformamide is cooled to 0° C. and treated with 267 mg (2.2 mol) of trimethylisocyanate. The reaction mixture is left to warm to RT and stirring is continued for 2 days. For the working-up, the suspension is evaporated under reduced pressure. The crude product is triturated in water, then the recovered solid material triturated a second time in a mixture of ethyl acetate and a saturated solution of sodium hydrogencarbonate. The remaining solid is collected on a filter funnel to give, after drying under high vacuum, 155 mg (61% of theory) of (R)-{1-[4-(3-fluoro-benzyloxy)-phenyl]-2-oxo-pyrrolidin-3-yl}-urea as a white solid; MS: m/e=344 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235581B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-bd15441a52cb408dab5bd8d5a21f49c5 |
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| Source note | uspto-grants-2007_06 |
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