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HRID 421756作成日:2026年10月27日

3-{[(3-Fluorophenyl)amino]sulfonyl}benzoic acid → N-(3-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide

https://huagongshe.com/reaction/421756

反応式

関与物質

役割名称HCID仕込み量
反応物3-{[(3-Fluorophenyl)amino]sulfonyl}benzoic acidHCID 766536—
反応物(6S)-1,4-Diazabicyclo(4.3.0)nonaneHCID 781249—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
溶媒2-MethyltetrahydrofuranHCID 7301—
溶媒DimethylacetamideHCID 31374—
生成物N-(3-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 46853382—

反応手順

To 3-{[(3-fluorophenyl)amino]sulfonyl}benzoic acid (0.9 g, 3.05 mmol) and 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (1.27 g, 3.35 mmol) in N,N-dimethylacetamide (6.4 mL) and 2-methyltetrahydrofuran (15 mL) was added (S)-octahydropyrrolo[1,2-a]pyrazine (0.55 g, 4.33 mmol) in 2-methyltetrahydrofuran (4 mL). The reaction was stirred at ambient temperature overnight and then diluted with 2-methyltetrahydrofuran (15 mL). The organic solution was washed with 6% NaHCO3/6% NaCl (10 mL), and the aqueous layer was extracted with 2-methyltetrahydrofuran (15 mL). The combined organic layers were washed with 6% NaHCO3/6% NaCl (10 mL), saturated NaCl (2×10 mL, 2×20 mL) and 1:1 saturated NaCl/water (2×20 mL), and then concentrated. The residue was concentrated from ethanol (2×10 mL) to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101614B2
出典データセットuspto-grants-2012_01
ORD IDord-ef128d2bb8a242ccb420c21dfbe69bf2
出典メモuspto-grants-2012_01