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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730705Generated: October 25, 2026

Potassium Carbonate → Tert-butyl 4-(3-chloropyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/730705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-DichloropyridineHCID 16988—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(3-chloropyridin-2-yl)piperazine-1-carboxylateHCID 11630777—

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2,3-dichloropyridine (10 g, 67.5 mmol, Aldrich), tert-butyl 1-piperazinecarboxylate (12.58 g, 67.5 mmol, Aldrich), copper powder (0.5 g, 7.8 mmol) and K2CO3 (9.33 g, 67.5 mmol) in DMF (100 mL) was stirred at 120° C. for 16 h. The reaction mixture was cooled to room temperature, concentrated in vacuo and the residue was dissolved in EtOAc (200 mL). The organic solution was washed with saturated aqueous solution of NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4, and filtered. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography, eluting with 15% EtOAc/hexane, to give the title compound as an orange oil. MS (ESI, pos. ion) m/z: 298 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582761B2
Source datasetuspto-grants-2009_09
ORD IDord-8ec3d2d97ed5457598894e4b83e37840
Source noteuspto-grants-2009_09