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HRID 79201Erstellt: 23. Oktober 2026

Potassium Carbonate → tert-Butyl 4-((6-chloropyridin-3-yl)methyl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/79201

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt2-Chloro-5-(chloromethyl)pyridineHCID 155479—
LösungsmittelAcetonitrileHCID 6342—
Produkttert-Butyl 4-((6-chloropyridin-3-yl)methyl)piperazine-1-carboxylateHCID 4578899384,7%

Reaktionsschritte

To a stirred suspension of 2-chloro-5-(chloromethyl)pyridine (2.0 g, 12 mmol) in acetonitrile (40 mL) was added potassium carbonate (1.5 mL, 25 mmol) followed by tert-butyl 1-piperazinecarboxylate (2.3 g, 12 mmol). The resulting mixture was stirred at room temperature for 20 h. Upon workup, the mixture was poured into ice and 2 N NaOH aqueous solution and extracted with ethyl acetate (2×). The combined organics were dried over Na2SO4 and concentrated in vacuo. The residue was subjected to combi-flash column chromatography (methanol/DCM) to give compound 339 (3.17 g, 82% yield) as a thick colorless liquid. 1H NMR 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.32 (1 H, d, J=2.0 Hz), 7.66 (1 H, d, J=7.4 Hz), 7.30 (1 H, d, J=8.2 Hz), 3.50 (2 H, s), 3.37-3.47 (4 H, m), 2.38 (4 H, br. s.), 1.46 (9 H, s). LCMS-ESI (POS), M/Z, M+1: Found 312.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841312B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-11d42e68f9ba40d8850ba8553b1c370c
Quellennotizuspto-grants-2014_09