HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412663Generated: October 25, 2026
Potassium Carbonate → (3R)-1-[(2-fluoro-4-pyridinyl)methyl]-3-piperidinol
https://huagongshe.com/reaction/412663
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3R)-piperidin-3-ol hydrochloride | HCID 2759333 | — |
| Reactant | 4-Bromomethyl-2-fluoropyridine | HCID 13985168 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (3R)-1-[(2-fluoro-4-pyridinyl)methyl]-3-piperidinol | HCID 53960603 | 88.8% |
Reaction Steps
(3R)-3-hydroxypiperidine hydrochloride (0.188 g) was added to a solution of 4-(bromomethyl)-2-fluoropyridine (0.26 g) [see Porter et al, WO 9622978] and potassium carbonate (0.189 g) in acetonitrile (15 ml). The reaction mixture was refluxed for 5 days, after which time the solvent was removed under reduced pressure and the residue partitioned between dichloromethane and water. The organic layer was separated and the aqueous was adjusted to pH 12 and the product extracted with dichloromethane. The combined organic layers were dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent system of 95:5, by volume, chloroform:methanol to afford (3R)-1-[(2-fluoro-4-pyridinyl)methyl]-3-piperidinol (0.255 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562964B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-4fa112c13c2b4921bf591958582113af |
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| Source note | uspto-grants-2003_05 |
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