HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 498047Generated: October 30, 2026
Methanesulfonic Acid → HCID 135848085, compound
https://huagongshe.com/reaction/498047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | HCID 22320218 | HCID 22320218 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 135848085 | HCID 135848085 | 74.4% |
Reaction Steps
A solution of methanesulfonic acid (20 mL, 0.31 mol) in phosphorus pentoxide (5.00 g, 35.2 mmol) was heated at 100° C. The mixture was stirred at the same temperature, while powdery 2-[[1-(2-pyridinyl)-1H-pyrazol-5-yl]amino]benzoic acid (1.94 g, 6.92 mmol) was added in small portions. The reaction mixture was heated and stirred at the same temperature for 10 minutes. The mixture was allowed to cool to room temperature, and iced water was added thereto. The solution was made basic by the addition of an aqueous sodium hydroxide solution, and the organic matter was extracted with ethyl acetate. The extract was washed with saturated brine and water, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue thus obtained was purified by silica gel column chromatography (chloroform:methanol=99:1) to give the title compound (1.35 g, 74% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06949648B2 |
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| Source dataset | uspto-grants-2005_09 |
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| ORD ID | ord-205a04f98130405cac2368c0a85b85a9 |
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| Source note | uspto-grants-2005_09 |
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