HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639591Generated: October 31, 2026
Water → propane-1-sulfonic acid {2-fluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl}-amide
https://huagongshe.com/reaction/1639591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5H-Pyrrolo[2,3-b]pyrazine | HCID 5370803 | — |
| Reactant | Propane-1-sulfonic acid (2-fluoro-3-formyl-phenyl)-amide | HCID 58086814 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | propane-1-sulfonic acid {2-fluoro-3-[hydroxy-(5H-pyrrolo[2,3-b]pyrazin-7-yl)-methyl]-phenyl}-amide | HCID 58001698 | 49% |
Reaction Steps
To propane-1-sulfonic acid (2-fluoro-3-formyl-phenyl)-amide (18, 50 mg, 0.42 mmol) in 0.8 mL of methanol, 5H-pyrrolo[2,3-b]pyrazine (3, 103 mg, 0.42 mmol) and potassium hydroxide (71 mg, 1.3 mmol) were added under an atmosphere of nitrogen. The reaction was stirred at room temperature for 48 hours, then poured into water and extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered and the filtrate concentrated under vacuum. The resulting material was purified by silica gel column chromatography eluting with 60% ethyl acetate in dichloromethane. Appropriate fractions were combined and concentrated under vacuum to provide the desired compound as a solid (19, 74 mg, 49%). MS (ESI) [M−H+]−=363.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110576B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-851285fb3ca945689f3e52db34a97085 |
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| Source note | uspto-grants-2012_02 |
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