HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400496Generated: October 25, 2026
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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-[(2-Fluorophenyl)sulfamoyl]benzoic acid | HCID 2318073 | — |
| Reactant | (8aR)-Octahydropyrrolo(1,2-a)pyrazine | HCID 7004239 | — |
| Solvent | 2-Methyltetrahydrofuran | HCID 7301 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N-(2-fluorophenyl)-3-[(8aR)-hexahydropyrrolo[1,2-a]pyrazin-2(1H)-ylcarbonyl]benzenesulfonamide | HCID 46853381 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741899B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-6e4348d19e1f49dea3c43bce0d0e1878 |
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| Source note | uspto-grants-2014_06 |
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