Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Acetonitrile chloroform | HCID 22555007 | — |
| Reactant | HCID 85218459 | HCID 85218459 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Sutezolid | HCID 465951 | 100% |
Reaction Steps
The [[3-[3-fluoro-4-(4-thiomorpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]-p-toluenesulfonate (2.0 g, 4.287 mmol) was dissolved in dry DMF (15 mL) and then treated with solid NaN3 (1.67 g, 25.722 mmol). The reaction was heated to 65° C. (external temperature) for 6 hours, after which the reaction was allowed to cool to ambient temperature, stirring over a long weekend (158 hours). At this point, the reaction was found to be complete by TLC (6% CH3CN/CHCl3, UV short wave). The reaction was diluted with EtOAc (300 mL) and then washed with water (3×250 mL). The aqueous portions were back-extracted with more EtOAc (2×150 mL). The EtOAc portions were combined, dried over Na2SO4, filtered and concentrated under reduced pressure to give 1.447 g (100%) of the title compound as an off-white solid with a melting point of 91.5°-93° C. and a HRMS (M+) calculated for C14 H16N5O5FS 337.1009, found 337.1009.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05688792 |
|---|
| Source dataset | uspto-grants-1997_11 |
|---|
| ORD ID | ord-f213aa0865dc4da590d7fd1a0f1b06c2 |
|---|
| Source note | uspto-grants-1997_11 |
|---|