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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174629Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 11689842, compound

https://huagongshe.com/reaction/1174629

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 21914515HCID 21914515—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 11689842HCID 11689842—

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-(tert-pentyl)nicotinamide (Intermediate 32, 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-(1,1-dimethylpropyl)-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-29f1a4b7648d4116a664b62e188ca83f
Source noteuspto-grants-2010_11