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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924277Generated: November 2, 2026

p-Chloroperbenzoic acid → HCID 15952963, compound

https://huagongshe.com/reaction/1924277

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chloroperbenzoic acidHCID 70299—
ReactantHCID 15952855HCID 15952855—
SolventChloroformHCID 6212—
ProductHCID 15952963HCID 1595296338%

Reaction Steps

4-chloroperbenzoic acid (36 mg, 0.134 mmol, 1 eq) is added to a solution of 1-{[6-(methylthio)-2-(trifluoromethyl)imidazo[1,2-b]pyridazin-3-yl]methyl}-4-propylpyrrolidin-2-one 33 (50 mg, 0.134 mmol) in chloroform (2 ml) at −30° C. After 30 minutes, the mixture is warmed to room temperature then stirred for additional 16 hours. After hydrolysis with a saturated aqueous NaHCO3 solution (2 ml) and extraction with CHCl3 (2 ml), the cumulated organic layers are dried over MgSO4 and condensed under reduced pressure. The resulting crude product is purified by reverse phase liquid chromatography (gradient acetonitrile/water/TFA) to yield 1-{[6-(methylsulfinyl)-2-(trifluoromethyl)imidazo[1,2-b]pyridazin-3-yl]methyl}-4-propylpyrrolidin-2-one 82.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-24fe2d67072545e49e0c4c117f168d40
Source noteuspto-grants-2012_05