Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 90373050 | HCID 90373050 | — |
| Reactant | HCID 178435178 | HCID 178435178 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 90380071 | HCID 90380071 | 88.5% |
Reaction Steps
To a polypropylene vial with cap was added (5)-tert-butyl 3-(6-bromo-3-fluoro-4-(triethylsilyl)pyridin-2-yl)-3-((R)-1,1-dimethylethylsulfinamido)-4-fluorobutanoate (9.8 g, 17.2 mmol), THF (50 mL) and DMF (50.0 mL). To the solution was added potassium fluoride (Aldrich; 2.75 g, 47.3 mmol) and acetic acid (2.71 mL, 47.3 mmol). The solution was stirred at rt for 17 h. The mixture was poured into sat NaHCO3 (200 mL) and then diluted with water (200 mL). The solution was extracted with EtOAc (3×100 mL) and the combined extracts were washed with water (3×100 mL) and brine (100 mL) and then dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (Gradient: 0.0 to 40% EtOAc/hexane, 120 g Silicycle column) afforded (5)-tert-butyl 3-(6-bromo-3-fluoropyridin-2-yl)-3-((R)-1,1-dimethylethylsulfinamido)-4-fluorobutanoate (6.93 g, 15.22 mmol, 88% yield) as a yellow oil. MS m/z=455.0 [M+H]+. Calculated for C17H25BrF2N2O3S: 454.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09296734B2 |
|---|
| Source dataset | uspto-grants-2016_03 |
|---|
| ORD ID | ord-189ff933b2f9411e9ff8b9c95cd87d61 |
|---|
| Source note | uspto-grants-2016_03 |
|---|