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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1864030생성일: 2026년 10월 26일

1,1'-Carbonyldiimidazole → tert-butyl 2-oxo-2-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)ethylcarbamate

https://huagongshe.com/reaction/1864030

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-(tert-butoxycarbonyl)glycineHCID 78288—
반응물1-phenyl-1H,2H,3H,4H-pyrrolo(1,2-a)pyrazineHCID 2770910—
반응물Boc-glycine imidazolideHCID 86621298—
용매1,2-DichloroethaneHCID 11—
생성물tert-butyl 2-oxo-2-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)ethylcarbamateHCID 6740196061.2%

반응 단계

(1.1 g, 7.0 mmol) of CDI were added to a solution of Boc-glycine (1.2 g, 6.7 mmol) in DCE (20 ml), and stirring was carried out for 100 min at RT. (1.3 g, 6.7 mmol) of 1-phenyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine (A2) were then added, and stirring was carried out for a further 2 h at RT. The mixture was then heated for 2 h at 50° C. (450 mg, 2 mmol) of Boc-glycine imidazolide were subsequently added, and the mixture was heated for 2 h under reflux. After cooling to RT, washing was carried out with, in succession, a 5% aq. sodium carbonate solution, a 5% aq. citric acid solution, water and brine. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. CC (DCE) with the residue yielded 1.4 g (4.1 mmol, 61%) of tert-butyl 2-oxo-2-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)ethylcarbamate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625900B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-9968b7d6be844da4914308379ccdf687
출처 메모uspto-grants-2009_12