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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168384Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 22992260, compound

https://huagongshe.com/reaction/1168384

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantAluminumHCID 5359268—
ReactantHCID 22172705HCID 22172705—
SolventChloroformHCID 6212—
ProductHCID 22992260HCID 22992260—

Reaction Steps

3-Chloroperbenzoic acid (3.7 g, 13.4 mmol) was added in 3 portions to a solution of 2-ethoxymethyl-1-phenylmethyl-1H-imidazo[4,5-c][1,5]naphthyridine (3.9 g, 12.2 mmol) in chloroform (100 mL) in a flask covered with aluminum foil. The reaction mixture was stirred at ambient temperature overnight; and then it was washed twice with dilute aqueous sodium bicarbonate and once with brine. The chloroform layer was divided into two portions. One portion was used in the example below. The second portion was concentrated under vacuum. The residue was recrystallized from isopropyl alcohol to provide 2-ethoxymethyl-1-phenylmethyl-1H-imidazo[4,5-c][1,5]naphthyridine-5-oxide as a solid, m.p. 187.5-189° C. Analysis: Calculated for C19H18N4O2+¼ H2O: %C, 67.52; %H, 5.49; %N, 16.58; Found: %C, 67.56; %H, 5.36; %N, 16.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624172B2
Source datasetuspto-grants-2003_09
ORD IDord-9a1be3ed713c4bfe86907574919bcbd3
Source noteuspto-grants-2003_09