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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406256생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/406256

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참여 물질

역할이름HCID투입량
반응물Lauroyl peroxideHCID 7773—
반응물N-bromobutanimideHCID 67184—
반응물tert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 86681860—
용매Carbon TetrachlorideHCID 5943—
생성물tert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylateHCID 66666005—

반응 조건

온도60 °C

반응 단계

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;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754085B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-429f4552b0764d83995f58ff50fdfc3c
출처 메모uspto-grants-2014_06