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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 57877Erstellt: 23. Oktober 2026

2-Bromo-6-fluoropyridine → tert-butyl N-[1-(6-bromo-2-pyridyl)-6-methyl-3-piperidyl]carbamate

https://huagongshe.com/de/reaction/57877

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Bromo-6-fluoropyridineHCID 639438—
Edukttert-butyl N-(6-methylpiperidin-3-yl)carbamateHCID 42609251—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkttert-butyl N-[1-(6-bromo-2-pyridyl)-6-methyl-3-piperidyl]carbamateHCID 8670707239%

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A solution containing 2-bromo-6-fluoropyridine (0.95 mL, 6.65 mmol and tert-butyl 6-methylpiperidin-3-ylcarbamate (750 mg, 3.32 mmol) in methyl sulfoxide 5.0 ml was heated 95° C. 18 h. The reaction was quenched with water then extracted with EtOAc. The organic layers was dried with sodium sulfate, filtered, and concentrated in vacuum. The crude product was purified by flash chromatography (EtOAc/Heptane eluted at 30% EtOAc) to give tert-butyl N-[1-(6-bromo-2-pyridyl)-6-methyl-3-piperidyl]carbamate (480 mg) in 39% yield. MS (ESI) m/z: 371.2

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09434725B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-3d401b61bbcc445dbb22ecc949716f4e
Quellennotizuspto-grants-2016_09