Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 86639862 | HCID 86639862 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86639861 | HCID 86639861 | — |
Reaction Steps
While being maintained at 0° C., KOH (0.13 g, 2.4 mmol) was added to a solution of the (S)—N-{{3-[3,5-difluoro-4-(7-hydroxydimono?-5-azaspiro[2,4]heptan-5-yl)phenyl]-2-oxo-5-oxazolidinyl}methyl}acetamide (0.8 g, 1.4 mmol) obtained in Example 3 in 10 mL of DMF, and then slowly droplets of ethyl bromide (0.4 mL, 5.6 mmol) were added with stirring for 3 hours. After the reaction terminated, the reaction mixture was poured into cold water and extracted with ethyl acetate. The organic phase was washed with water and brine and dehydrated over anhydrous magnesium sulfate. Purification through flash column chromatography (n-hexane/ethyl acetate=1:4) afforded the target compound in a white pure form (0.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08168797B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-7cfb43ec44584a7cb75e1c7428cf5b31 |
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| Source note | uspto-grants-2012_05 |
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