戻る
化工社化工社 化学情報印刷レポート · 研究参考用
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

反応式

関与物質

役割名称HCID仕込み量
反応物3-[(2-Fluorophenyl)sulfamoyl]benzoic acidHCID 2318073—
反応物(8aR)-Octahydropyrrolo(1,2-a)pyrazineHCID 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-MethyltetrahydrofuranHCID 7301—
溶媒DimethylacetamideHCID 31374—
生成物N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08404719B2
出典データセットuspto-grants-2013_03
ORD IDord-561d5189ea4e45b694e1479698e5da8c
出典メモuspto-grants-2013_03