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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1616072Erstellt: 25. Oktober 2026

(S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamate → Tert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamate

https://huagongshe.com/reaction/1616072

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamateHCID 58318617—
Edukt(2-Amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanoneHCID 69673444—
KatalysatorSodium tetrachloroaurate dihydrateHCID 18949434—
LösungsmittelIsopropanolHCID 3776—
ProduktTert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamateHCID 67599683—

Reaktionsschritte

A solution of (2-amino-5-fluorophenyl)(3-methylpyridin-2-yl)methanone (0.29 g, 1.26 mmol), (S)-tert-butyl 3-oxo-4-(pyridin-2-yl)butan-2-ylcarbamate (0.366 g, 1.386 mmol), and sodium tetrachloroaurate(iii) dihydrate (0.025 g, 0.063 mmol) in 2-propanol (5.0 mL) was stirred at 80° C. for 24 h under an argon atmosphere, then at room temperature for an additional 48 h. The solution was purified by silica gel column chromatography eluting with a gradient of 10-40% EtOAc in hexane to afford tert-butyl 1-(6-fluoro-4-(3-methylpyridin-2-yl)-3-(pyridin-2-yl)quinolin-2-yl)ethylcarbamate as a dark solid: LC-MS (ESI) m/z 459.2 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08765768B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-1f1e2d5cffe2438a81af4ee358475eae
Quellennotizuspto-grants-2014_07