HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288231Generated: October 29, 2026
Methanesulfonyl chloride → HCID 15428650, compound
https://huagongshe.com/reaction/2288231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 15428649 | HCID 15428649 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 15428650 | HCID 15428650 | — |
Reaction Steps
A solution of 4-(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-amine prepared as set forth in Example 2 (200 mg, 0.77 mmol) and methanesulfonyl chloride (90 mg) in pyridine (5 ml) was stirred at room temperature overnight. The pyridine was removed in vacuo and the residue was treated with methylene chloride and water. The resultant precipitate was filtered to give N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide. Additional N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide was contained in the methylene chloride layer. The methylene chloride was stripped in vacuo and the residue purified by chromatography on silica gel using mixtures of ethyl acetate and methanol as eluents. The purified N-[4(4-fluorophenyl)-5-(4-pyridinyl)-1H-pyrazol-3-yl]methanesulfonamide had m.p. 168-170° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06087496 |
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| Source dataset | uspto-grants-2000_07 |
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| ORD ID | ord-985503b063574ce9bd502b552612a808 |
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| Source note | uspto-grants-2000_07 |
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