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HRID 1951488作成日:2026年10月26日
3-[(2-Fluorophenyl)sulfamoyl]benzoic acid → N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide
https://huagongshe.com/reaction/1951488
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 3-[(2-Fluorophenyl)sulfamoyl]benzoic acid | HCID 2318073 | — |
| 反応物 | (8aR)-Octahydropyrrolo(1,2-a)pyrazine | HCID 7004239 | — |
| 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-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide | HCID 46853381 | — |
反応手順
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-b]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-α]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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08404719B2 |
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| 出典データセット | uspto-grants-2013_03 |
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| ORD ID | ord-561d5189ea4e45b694e1479698e5da8c |
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| 出典メモ | uspto-grants-2013_03 |
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