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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240239생성일: 2026년 10월 23일

(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid → Quinoxaline

https://huagongshe.com/ko/reaction/240239

반응식

참여 물질

역할이름HCID투입량
반응물(2S,4R)-4-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acidHCID 88804—
반응물TrimethylsilyldiazomethaneHCID 167693—
반응물HCID 86663289HCID 86663289—
반응물sodium 2-methylpropan-2-olateHCID 178418730—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물QuinoxalineHCID 7045283.8%

반응 단계

To a solution of N-Boc-trans-4-hydroxy-L-proline 2-11 (2.404 g, 10.396 mmol) in DMF (14 ml) and THF (60 ml) at 0° C. was added t-BuONa (3.0 g, 31.189 mmol) portionwise. The reaction mixture was allowed to warm up to rt. After stirring for 1 h, the mixture was cooled down to 0° C. and 2-chloro-3-(1,1-difluoroallyl)quinoxaline 2-10 (2.45 g, ˜10.396 mmol) was added and warmed up to rt. After stirring for 4 h, the reaction mixture was quenched with 1 N HCl at 0° C. The aqueous layer was extracted with EtOAc (3×), and the organic layer was combined, washed with water, brine, dried and concentrated in vacuo. To the residue in DCM (50 ml) and MeOH (10 ml) was added TMSCHN2 (10.4 ml, 20.792 mmol, 2.0 M in Hexane). The solution was stirred at rt for 30 min then concentrated in vacuo. The residue was purified by flash chromatography on CombiFlash with Hexane to 30% ethyl acetate in hexane to afford desired product 1-1 (3.84 g, 82%). MS (ESI): m/z=450.24 [M+H].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648037B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-b348e6af68bc4f7d86d9695c1bb4c92d
출처 메모uspto-grants-2014_02