HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174625Generated: November 2, 2026
m-Chloroperbenzoic acid → HCID 11516560, compound
https://huagongshe.com/reaction/1174625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 6-[5-[(Cyclopropylamino)carbonyl]-3-fluoro-2-methylphenyl]-N-(2-methylpropyl)-3-pyridinecarboxamide | HCID 21914620 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 11516560 | HCID 11516560 | — |
Reaction Steps
mCPBA (57-86%, 15 mg) was added to a solution of 6-(5-cyclopropylcarbamoyl-3-fluoro-2-methyl-phenyl)-N-(2-methylpropyl)-nicotinamide (Intermediate 30, 20 mg) in chloroform (3 ml) at 60° C. and the reaction maintained at 60° C. for 7 hrs. The reaction was allowed to cool, diluted with methanol, and passed through an aminopropyl SPE (2 g) and an SCX SPE (1.0 g). The filtrate was reduced to dryness under vacuum and the residue triturated with ether to give 6-{5-[(cyclopropylamino)carbonyl]-3-fluoro-2-methylphenyl}-N-(2-methylpropyl)-3-pyridinecarboxamide 1 oxide as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838540B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-3c4ef4d1f66a48959123acde3db13ce0 |
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| Source note | uspto-grants-2010_11 |
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