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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 909253생성일: 2026년 10월 26일

Succinic anhydride → 4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acid

https://huagongshe.com/reaction/909253

반응식

참여 물질

역할이름HCID투입량
반응물Succinic anhydrideHCID 7922—
반응물TriethylamineHCID 8471—
반응물1-phenyl-1H,2H,3H,4H-pyrrolo(1,2-a)pyrazineHCID 2770910—
반응물Ethylacetate methanolHCID 21584119—
용매AcetonitrileHCID 6342—
용매Ethyl AcetateHCID 8857—
생성물4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acidHCID 4277933344%

반응 단계

1-Phenyl-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine (A2) (396 mg, 2.0 mmol) and NEt3 (277 μl, 2.0 mmol) were added to a suspension of succinic anhydride (176 mg, 1.76 mmol) in MeCN (28 ml), and stirring was carried out for 16 h at RT. The mixture was then diluted with EA (30 ml) and washed with 2N hydrochloric acid (2×5 ml). The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The resulting residue was taken up in EA (50 ml) and again washed with 2N hydrochloric acid (20 ml) and then with a sat. aq. sodium carbonate solution (2×30 ml). The organic phase was again dried over MgSO4, filtered and concentrated in vacuo. CC (EA/MeOH 3:1) with the residue yielded 230 mg (0.77 mmol, 44%) of 4-oxo-4-(1-phenyl-3,4-dihydropyrrolo[1,2-a]pyrazin-2(1H)-yl)butanoic acid (S3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08017772B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-471bfbf9f1d94d26aafab6e253d4ad81
출처 메모uspto-grants-2011_09