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HRID 400499作成日:2026年10月26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/400499
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-{[(3-Fluorophenyl)amino]sulfonyl}benzoic acid | HCID 766536 | — |
| 反応物 | (6S)-1,4-Diazabicyclo(4.3.0)nonane | HCID 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-Methyltetrahydrofuran | HCID 7301 | — |
| 溶媒 | Dimethylacetamide | HCID 31374 | — |
| 生成物 | N-(3-fluorophenyl)-3-[(8aS)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08741899B2 |
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| 出典データセット | uspto-grants-2014_06 |
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| ORD ID | ord-3076e350e6064c0f99ddcf10cd644fdb |
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| 出典メモ | uspto-grants-2014_06 |
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