HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 2-Fluoro-3-(4-fluorotetrahydro-2H-pyran-4-YL)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | 4-(3-Fluoropyrazin-2-YL)tetrahydro-2H-pyran-4-OL | HCID 59351230 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Fluoro-3-(4-fluorotetrahydro-2H-pyran-4-YL)pyrazine | HCID 59351135 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 4-(3-fluoropyrazin-2-yl)tetrahydro-2H-pyran-4-ol (0.4 g, 2.018 mmol) in CH2Cl2 (6.73 mL) was cooled to 0° C. DAST (0.533 mL, 4.04 mmol) was added to the reaction mixture dropwise and the resulting mixture was allowed to stir at 0° C. for 2 hr. A solution of saturated sodium carbonate was added dropwise to the reaction mixture at 0° C. to quench the reaction. The heterogeneous mixture was stirred vigorously for 1 hr to ensure complete quenching. Mixture was transferred to a separatory funnel and the layers were separated after addition of more DCM and saturated bicarbonate solution. The organic layer was dried over magnesium sulfate and rotovapped to remove the volatile solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08053438B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-dcea7773ec704679b5d4c91fa4e9dd9b |
| Source note | uspto-grants-2011_11 |