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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505388Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 178493206, compound

https://huagongshe.com/reaction/505388

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178493197HCID 178493197—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 178493206HCID 17849320693%

Reaction Steps

2-(((4-Methoxy-3-methyl-2-pyridinyl)methyl)thio)-6-methyl-5-(2,2,2-trifluoroethoxy)-3H-imidazo[4,5-b]pyridine (270 mg, 0.68 mmol) was dissolved in a mixture of methanol (2 ml) and toluene (18 ml), and a solution of metachloroperbenzoic acid (162 mg) in a mixture of methanol (0.5 ml) of toluene (0.5 ml) were added dropwise at −40° C. under nitrogen flow. After stirred at −20° C. to −40° C. for 2 hours, a sodium bicarbonate solution was added, the mixture was extracted with chloroform (30 ml), and dried over sodium sulfate. The solvent was evaporated, and the solid was precipitated from a mixture of chloroform and n-hexane to yield the title compound (263 mg, 0.63 mmol, 93%) as a purple gray solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781452B2
Source datasetuspto-grants-2010_08
ORD IDord-6d0d1146482a438d95521c61603625c9
Source noteuspto-grants-2010_08