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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 406256Erstellt: 25. Oktober 2026

Lauroyl peroxide → tert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylate

https://huagongshe.com/reaction/406256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLauroyl peroxideHCID 7773—
EduktN-bromobutanimideHCID 67184—
Edukttert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 86681860—
LösungsmittelCarbon TetrachlorideHCID 5943—
Produkttert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 66666005—

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a stirred solution of tert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylate (step 1)(25 g, 64.5 mmol) in carbon tetrachloride (645 ml) at RT under N2 was added NBS (13.78 g, 77 mmol) followed directly by lauroyl peroxide (0.257 g, 0.645 mmol) and the solution was heated at 60° C. for 4 h 15 mins. The mixture was filtered through filter paper and the filtrate was washed with sat. NaHCO3 (300 ml), 2 M Na2SO3 (300 ml) and sat. brine (300 ml). The solution was dried over MgSO4 and filtered, washing MgSO4 bed with DCM (100 ml). The solvent was removed in vacuo. The crude product was dissolved in diethyl ether (300 ml) and was allowed to stand at RT and placed in a fridge overnight. The resulting crystalline solid was isolated by decanting off the mother liquors. The crystals were washed with diethyl ether to afford the title compound. Further product was obtained by chromatography of the mother liquors eluting with iso-hexane/EtOAc to afford the title product;

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754085B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-429f4552b0764d83995f58ff50fdfc3c
Quellennotizuspto-grants-2014_06