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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 400496생성일: 2026년 10월 25일

3-[(2-Fluorophenyl)sulfamoyl]benzoic acid → N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/400496

반응식

참여 물질

역할이름HCID투입량
반응물3-[(2-Fluorophenyl)sulfamoyl]benzoic acidHCID 2318073—
반응물(8aR)-Octahydropyrrolo(1,2-a)pyrazineHCID 7004239—
용매2-MethyltetrahydrofuranHCID 7301—
용매DimethylacetamideHCID 31374—
생성물N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46853381—

반응 단계

To a mixture of 3-{[(2-fluorophenyl)amino]sulfonyl}benzoic acid (800 mg, 2.71 mmol) and 2-(3H-[1,2,3]triazolo[4,5-h]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (1133 mg, 2.98 mmol) in N,N-dimethylacetamide (6.5 mL) and 2-methyltetrahydrofuran (19.5 mL) was added (R)-octahydropyrrolo[1,2-a]pyrazine (479 mg, 3.79 mmol). The reaction was stirred at room temperature for 3 hours, diluted with 2-methyltetrahydrofuran (5 mL), and washed with saturated bicarbonate (2×25 mL). The combined aqueous layers were adjusted to pH 7 with buffer and re-extracted with 2-methyltetrahydrofuran (3×15 mL). The combined organic layers were concentrated under reduced pressure. The residue was taken up in ethanol (25 mL) and concentrated to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08741899B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-6e4348d19e1f49dea3c43bce0d0e1878
출처 메모uspto-grants-2014_06