HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 11149549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 11149549 | HCID 11149549 | 58% |
Reaction Steps
Sodium hydride (56 mg, 2.3 mmol) was added to a solution of piperidin-4-ol (214 mg, 2.11 mmol) in DMSO (8 mL). After stirring for 30 minutes, 2,5-dibromopyridine was added. After stirring for 24 hours, sodium hydride (56 mg, 2.3 mmol) was added. After stirring for another 24 hours the reaction was partitioned between ethyl acetate and water. The phases were separated and the aqueous phase was extracted with ethyl acetate. The combined organic phases were dried over MgSO4 and concentrated by rotary evaporation. The residue was purified by silica gel chromatography using gradient elution of dichloromethane, methanol, ammonium hydroxide to afford 5-bromo-2-(piperidin-4-yloxy)-pyridine (316 mg, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08785632B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-f5b7b399bd8941f299303e317472bca3 |
| Source note | uspto-grants-2014_07 |