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HRID 406256作成日:2026年10月26日

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

https://huagongshe.com/reaction/406256

反応式

関与物質

役割名称HCID仕込み量
反応物Lauroyl peroxideHCID 7773—
反応物N-bromobutanimideHCID 67184—
反応物tert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 86681860—
溶媒Carbon TetrachlorideHCID 5943—
生成物tert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 66666005—

反応条件

温度60 °C

反応手順

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;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754085B2
出典データセットuspto-grants-2014_06
ORD IDord-429f4552b0764d83995f58ff50fdfc3c
出典メモuspto-grants-2014_06