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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 60234Erstellt: 25. Oktober 2026

Cesium carbonate → Tert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamate

https://huagongshe.com/reaction/60234

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCesium carbonateHCID 10796—
Edukttert-Butyl carbamateHCID 77922—
Edukt5-Bromo-2-chloro-3-fluoropyridineHCID 2763285—
Katalysator1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
KatalysatorTris(dibenzylideneacetone) dipalladiumHCID 9832798—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktTert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamateHCID 8665604086%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

A degassed mixture of 5-bromo-2-chloro-3-fluoropyridine (22.5 g, 107 mmol), tert-butyl carbamate (13.8 g, 117.5 mmol), tris(dibenzylideneacetone) dipalladium(0) (2.95 g, 3.2 mmol), XantPhos (2.48 g, 4.28 mmol) and cesium carbonate (69.7 g, 214 mmol) in dioxane (340 mL) was heated at 85° C. for 24 hours. The reaction mixture was cooled to ambient temperature and the resultant solid was removed by filtration. The resultant solid was washed with ethyl acetate followed by dichloromethane and the filtrate was combined and concentrated in-vacuo to afford a residue that was purified by flash chromatography (silica: cyclohexane to 25% ethyl acetate/cyclohexane) to afford the title compound as a pale yellow solid (22.6 g, 86%). 1H NMR (300 MHz, CDCl3): 8.04 (dd, J=10.1, 2.4 Hz, 1H), 7.98 (d, J=2.4 Hz, 1H), 6.62 (s, 1H), 1.53 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09440976B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-2aad88eff7364f1f9f9968439896e0fc
Quellennotizuspto-grants-2016_09