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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174628Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 11596776, compound

https://huagongshe.com/reaction/1174628

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 44480443HCID 44480443—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 11596776HCID 11596776—

Reaction Conditions

Temperature60 °C

Reaction Steps

mCPBA (57-86%, 15 mg) was added to a solution of 6-{5-[(cyclopropylamino)carbonyl]-3-fluoro-2-methylphenyl}-N-[(1R)-1,2,2-trimethylpropyl]-3-pyridinecarboxamide (Intermediate 10, 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-[(1R)-1,2,2-trimethylpropyl]-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-b42064007721485cb98570069ee66f52
Source noteuspto-grants-2010_11