HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869133Generated: October 31, 2026
Potassium Carbonate → (1-(3-Bromo-5-fluoropyridin-4-yl)piperidin-4-yl)(4-methylpiperazin-1-yl)methanone
https://huagongshe.com/reaction/869133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (4-Methylpiperazin-1-yl)piperidin-4-yl-methanone dihydrochloride | HCID 45036889 | — |
| Reactant | 3-Bromo-4-chloro-5-fluoropyridine hydrochloride | HCID 86720940 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (1-(3-Bromo-5-fluoropyridin-4-yl)piperidin-4-yl)(4-methylpiperazin-1-yl)methanone | HCID 86720941 | — |
Reaction Steps
A mixture of (4-methylpiperazin-1-yl)-(4-piperidyl)methanone dihydrochloride (50.65 g, 178.2 mmol), 3-bromo-4-chloro-5-fluoro-pyridine hydrochloride 18 (40 g, 162 mmol) and dipotassium carbonate (94.04 g, 680.4 mmol) in NMP (400 mL) was heated at 150° C. overnight. The mixture was cooled to room temperature then filtered to remove inorganic salts and the filtrate was concentrated in vacuo. The residue was dissolved in EtOAc (800 mL), washed with brine (100 mL×4), dried (MgSO4), filtered and concentrated in vacuo to afford a brown viscous oil. This residue was purified by silica gel column (approx 800 g of silica), product loaded onto silica in DCM, then eluting with 3% methanol (containing 10% ammonium hydroxide)/DCM to afford the desired product as a brown oil which crystallised on standing (27.44 g, 44%). MS (ES+) 387.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969360B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-83a209c03b3e4e5abf368e5d942eac8c |
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| Source note | uspto-grants-2015_03 |
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