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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2276600Generated: October 27, 2026

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

https://huagongshe.com/reaction/2276600

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLauroyl peroxideHCID 7773—
ReactantN-bromobutanimideHCID 67184—
Reactanttert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 86681860—
SolventCarbon TetrachlorideHCID 5943—
Producttert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 66666005—

Reaction Conditions

Temperature60 °C

Reaction Steps

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;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09132127B2
Source datasetuspto-grants-2015_09
ORD IDord-f9b4f4351f9942c9af24caa44e33fdab
Source noteuspto-grants-2015_09