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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1465468Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1465468

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktPotassium CarbonateHCID 11430—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt5-Bromopyridine-2-carbonitrileHCID 817154—
LösungsmittelDimethylformamideHCID 6228—
ProduktTert-butyl 4-(6-cyanopyridin-3-yl)piperazine-1-carboxylateHCID 6703021174%

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08999989B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-a5d1d698b94045d8850b11c2a3c02f10
Quellennotizuspto-grants-2015_04