Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Oxetane, 3-(bromomethyl)-3-methyl- | HCID 144860 | — |
| Reactant | HCID 7046987 | HCID 7046987 | — |
| Reactant | HCID 178471823 | HCID 178471823 | — |
| Reactant | HCID 178524627 | HCID 178524627 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67362914 | HCID 67362914 | — |
Reaction Steps
101 mg (0.245 mmol) of (S)-3-{[1-(2-fluoro-phenyl)-5-hydroxy-1H-pyrazole-3-carbonyl]-amino}-3-(2-methyl-phenyl)-propionic acid ethyl ester (prepared from 1-(2-fluoro-phenyl)-5-hydroxy-1H-pyrazole-3-carboxylic acid and ethyl (S)-3-amino-3-(2-methyl-phenyl)-propionate analogously as described in synthesis example 2) were dissolved in 3 ml of DMF, and 160 mg (0.5 mmol) of cesium carbonate and 41.3 mg (0.245 mmol) of 3-bromomethyl-3-methyl-oxetane were added. The mixture was stirred for 4 h at 65° C. After evaporation of the solvent the residue was subjected to an aqueous work-up with EA and 10% aqueous solution of citric acid. After removal of the solvent from the organic phase 100 mg (82%) of the product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664257B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-132f037d98284b49bdc95c541086d538 |
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| Source note | uspto-grants-2014_03 |
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