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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465468Generated: October 26, 2026

Ethyl Acetate → Tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1465468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
Reactant5-Bromopyridine-2-carbonitrileHCID 817154—
SolventDimethylformamideHCID 6228—
ProductTert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 6703021174%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-bromopyridine-2-carbonitrile (551.3 mg, 3.012 mmol) in anhydrous dimethylformamide (6.0 ml) were added tert-butyl piperazine-1-carboxylate (670.6 mg, 3.601 mmol) and potassium carbonate (829.0 mg, 5.998 mmol). The mixture was stirred at 120° C. for 63 hrs and cooled to room temperature. Ethyl acetate (30 ml) was added, and the precipitate was collected by filtration. Water (30 ml) was added to the filtrate, and the precipitated solid was collected by filtration and dried under reduced pressure to give tert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylate (642.9 mg, yield 74.0%) as a slightly yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-a5d1d698b94045d8850b11c2a3c02f10
Source noteuspto-grants-2015_04