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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401573Erstellt: 23. Oktober 2026

Potassium Carbonate → [6-(4-Cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl ester

https://huagongshe.com/de/reaction/401573

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Cyanophenylboronic acidHCID 2734326—
EduktTert-butyl (6-bromopyridin-2-YL)carbamateHCID 13040380—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelN,N-Dimethylformamide--water (1/1)HCID 21962138—
Produkt[6-(4-Cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl esterHCID 6713369160%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of 4-cyanobenzeneboronic acid (7.35 g, 50 mmol), (6-bromo-pyridin-2-yl)carbamic acid tert-butyl ester (13.8 g, 50 mmol), Pd(Ph3P)4 (5.8 g, 0.15 mmol) and K2CO3 (10.4 g, 75 mmol) in DMF/H2O (1:1, 250 mL) was stirred under argon at 80° C. overnight. DMF was evaporated off under reduced pressure and the residue was dissolved in EtOAc (200 mL). The mixture was washed with water and brine, dried over Na2SO4, and concentrated to dryness. The residue was purified by column (Petroleum Ether/EtOAc 50:1) on silica gel to give [6-(4-cyano-phenyl)-pyridin-2-yl]carbamic acid tert-butyl ester (7.0 g, 60%). 1H NMR (300 MHz, CDCl3) δ 8.02-8.07 (m, 2H), 7.95 (d, J=8.4 Hz, 1H), 7.71-7.79 (m, 3H), 7.37-7.44 (m, 2H), 1.53 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741933B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-fff1aa13543d4ff4b374fb4abf25f113
Quellennotizuspto-grants-2014_06