HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447448Generated: October 29, 2026
Potassium Carbonate → 1-(5-Bromopyridin-2-yl)piperidin-4-ol
https://huagongshe.com/reaction/447448
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(5-Bromopyridin-2-yl)piperidin-4-ol | HCID 21897837 | 493.5% |
Reaction Steps
A mixture of 2,5-dibromopyridine (100 mg, 0.42 mmol), 4-hydroxypiperidine (49 mg, 0.46 mmol) and K2CO3 (64 mg, 0.46 mmol) in ethanol (4 mL) was heated to 110° C. for 52 h. The crude reaction mixture was concentrated under reduced pressure to dryness and the residue was treated with water. Crude product was collected by vacuum filtration and purified by flash chromatography using EtOAc/hexanes (1:4 to 2:3) to give the title compound as a white solid (533 mg, 41%). 1H NMR (400 MHz, CDCl3) δ 8.18 (d, J=2.2 Hz, 1H), 7.53 (dd, J=9.0, 2.3 Hz, 1H), 6.59 (d, J=9.0 Hz, 1H), 4.04-3.94 (m, 3H), 3.18 (t, J=11 Hz, 2H), 2.00-1.95 (m, 2H), 1.63-1.54 (m, 2H); MS ESI 256.9 [M+H]+, calcd for [C10H13BrN2O+H]+ 257.02.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481525B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-eecc8658ff3542a5ac4cb654d8cfb506 |
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| Source note | uspto-grants-2013_07 |
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