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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505382Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 178493207, compound

https://huagongshe.com/reaction/505382

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178493198HCID 178493198—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 178493207HCID 17849320780%

Reaction Conditions

Temperature-30 °C

Reaction Steps

5-Methoxy-2-(((4-methoxy-3-methyl-2-pyridinyl)methyl)thio)-6-methyl-3H-imidazo[4,5-b]pyridine (784 mg, 2.37 mmol) was dissolved in a mixture of methanol (6 ml) and toluene (54 ml). Metachloroperbenzoic acid (566 mg) in a mixture solution of methanol (3 ml) and toluene (3 ml) were added thereto at −40° C. under nitrogen flow, and the reaction mixture was stirred at −20 to −40° C. for 2 hours. After the reaction was completed, a sodium bicarbonate solution was added, and the organic layer was separated. The aqueous layer was extracted with chloroform (40 ml), combined with the organic layer and dried over sodium sulfate, the solvent was evaporated and the residue was obtained which was then precipitated as a solid from a mixture of chloroform and ether, thereby yielding the title compound (654 mg, 1.89 mmol, 80%) as a purple gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781452B2
Source datasetuspto-grants-2010_08
ORD IDord-2568e47dce054823b8d47ac02a600c81
Source noteuspto-grants-2010_08