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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lauroyl peroxide | HCID 7773 | — |
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | tert-Butyl 2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylate | HCID 86681860 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 생성물 | tert-Butyl 8-bromo-2,3-diphenyl-7,8-dihydropyrido[2,3-b]pyrazine-5(6H)-carboxylate | HCID 66666005 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08754085B2 |
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| 출처 데이터셋 | uspto-grants-2014_06 |
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| ORD ID | ord-429f4552b0764d83995f58ff50fdfc3c |
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| 출처 메모 | uspto-grants-2014_06 |
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