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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273757Generated: October 30, 2026

Potassium Carbonate → Tert-butyl 4-((4-(4-chlorophenyl)-6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2273757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-(Bromomethyl)-4-(4-chlorophenyl)-2-fluoropyridineHCID 67227341—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-((4-(4-chlorophenyl)-6-fluoropyridin-3-yl)methyl)piperazine-1-carboxylateHCID 67227318—

Reaction Steps

A mixture of EXAMPLE 307B (1.24 g), tert-butyl piperazine-1-carboxylate (0.768 g), and potassium carbonate (0.570) in N,N-dimethylformamide (20 mL) was stirred at room temperature for 2 hours. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was separated, and the aqueous layer was extracted with additional ethyl acetate three times. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified with flash column chromatography on silica gel using 10% ethyl acetate in hexanes to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09125913B2
Source datasetuspto-grants-2015_09
ORD IDord-ef89c2e677e54c35aa2eacdddb032c51
Source noteuspto-grants-2015_09