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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174625Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 11516560, compound

https://huagongshe.com/reaction/1174625

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-[5-[(Cyclopropylamino)carbonyl]-3-fluoro-2-methylphenyl]-N-(2-methylpropyl)-3-pyridinecarboxamideHCID 21914620—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 11516560HCID 11516560—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838540B2
Source datasetuspto-grants-2010_11
ORD IDord-3c4ef4d1f66a48959123acde3db13ce0
Source noteuspto-grants-2010_11