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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440245Generated: November 2, 2026

Potassium Carbonate → HCID 19973443, compound

https://huagongshe.com/reaction/1440245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 19973464HCID 19973464—
Catalystm-Chloroperbenzoic acidHCID 70297—
SolventDichloromethaneHCID 6344—
ProductHCID 19973443HCID 1997344379.7%

Reaction Steps

4.95 g of the 6-((4-chlorobutyl)thiomethyl)-2-methylimidazo[1,2-a]pyridine prepared in the Preparative Example 17 was dissolved in 50 ml of dichloromethane, followed by the cooling of the obtained solution with ice. A solution of 3.18 g of m-chloroperbenzoic acid in 20 ml of dichloromethane was dropped into the resulting solution in 20 minutes. After one hour, 0.16 g of m-chloroperbenzoic acid was further added to the obtained mixture. The obtained mixture was additionally stirred for 30 minutes, followed by the addition of an aqueous solution of sodium thiosulfate. The obtained mixture was vigorously stirred at room temperature for 15 minutes, followed by the addition of an aqueous solution of potassium carbonate. The obtained mixture was extracted with dichloromethane. The organic phase was dried over anhydrous potassium carbonate and distilled to remove the solvent. The residue was purified by silica gel column chromatography [solvent: dichloromethane/methanol (50:1 to 80:1)] to give 4.18 g of the title compound as a pale-pink solid (yield: 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498634
Source datasetuspto-grants-1996_03
ORD IDord-63554cd10d9a460aa464ec1eeed2ecea
Source noteuspto-grants-1996_03