HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479667Generated: October 30, 2026
Nitrogen → 4-(6-Bromo-2-pyridinyl)-1-methyl-4-piperidinol
https://huagongshe.com/reaction/479667
Participants
| Role | Name | HCID | Charge |
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| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 4-Methylpiperidin-2-one | HCID 14146878 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | 4-(6-Bromo-2-pyridinyl)-1-methyl-4-piperidinol | HCID 18772002 | — |
Reaction Steps
To a solution of 1.07 M n-BuLi (36.4 mL) and dry THF (200 mL) chilled to −70° C. under a blanket of N2 was added 2,6-dibromopyridine (10 g, 38.9 mmol)in 50 mL of dry THF slowly to maintain a temperature less than −69° C. Stirred at −70° C. for 20 min. Added 4-methylpiperidone (4.8 mL, 38.9 mmol) and stirred the mixture at −70° C. for 1 h. Quenched with saturated NaHCO3 and extracted with EtOAc. Washed the organic layer with brine, dried (MgSO4) and concentrated in vacuo to give 6-bromo-1′-methyl-2′,3′,5′,6′-tetrahydro-1′H-[2,4′]bipyridinyl-4′-ol as a light-yellow solid. MS m/z: 272.3 (M+H). Calc'd for C11H15BrN2O-271.15.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06645990B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-b7d7bea7d38042e9ac2866af4be2967c |
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| Source note | uspto-grants-2003_11 |
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