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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1285220Generated: October 26, 2026

m-Chloroperbenzoic acid → HCID 178510664, compound

https://huagongshe.com/reaction/1285220

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Fluorobenzoyl chlorideHCID 74376—
ReactantPyridine-4-carbonyl chlorideHCID 417436—
ReactantN-(5-cyano-1H-imidazol-4-yl)-4-pyridinecarboxamideHCID 13588467—
SolventEthyl AcetateHCID 8857—
ProductHCID 178510664HCID 178510664—

Reaction Steps

To a stirred suspension of N-(5-cyano-1H-imidazol-4-yl)-4-pyridinecarboxamide (0.53 g, 0.0025 mole), which can be made by the procedure of Example 1 substituting isonicotinoyl chloride for the 3-fluorobenzoyl chloride, in 20 ml of ethyl acetate was added 3-chloroperbenzoic acid (0.65 g, 0.003 mole). The mixture was heated at reflux for 15 hours, cooled and the solid product collected by filtration. The solid was washed with ethyl acetate and dried under reduced pressure to give N-(5-cyano-1H-imidazol-4-yl)-4-pyridinecarboxamide N-oxide (0.52 g; mp, 290°).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04565875
Source datasetuspto-grants-1986_01
ORD IDord-9a85c6bd15f84c62a47eddf82f890510
Source noteuspto-grants-1986_01