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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Methylpiperazin-1-yl)piperidin-4-yl-methanone dihydrochlorideHCID 45036889—
Reactant3-Bromo-4-chloro-5-fluoropyridine hydrochlorideHCID 86720940—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(1-(3-Bromo-5-fluoropyridin-4-yl)piperidin-4-yl)(4-methylpiperazin-1-yl)methanoneHCID 86720941—

Reaction Conditions

Temperature150 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969360B2
Source datasetuspto-grants-2015_03
ORD IDord-83a209c03b3e4e5abf368e5d942eac8c
Source noteuspto-grants-2015_03