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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890829Generated: October 29, 2026

Potassium Carbonate → K-604

https://huagongshe.com/reaction/890829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10384617HCID 10384617—
Reactant2-Bromo-N-(6-methyl-2,4-bis(methylthio)pyridin-3-yl)acetamideHCID 22247149—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductK-604HCID 989228891.6%

Reaction Steps

1-[2-(Benzimidazol-2-ylthio)ethyl]piperazine trihydrochloride 1.0 g (2.69 mmol) was suspended in acetonitrile (30 mL), and potassium carbonate 1.45 g (10.49 mmol) was added to the suspension. Water (8 mL) was added dropwise to the mixture under stirring at room temperature until the entirety of the suspension assumed a homogeneous solution. Subsequently, N-[2,4-bis(methylthio)-6-methylpyridin-3-yl]-2-bromoacetamide 810 mg (2.52 mmol) was gradually added to the mixture, and the mixture was stirred for 2.5 hours at room temperature. The reaction mixture was diluted with water (50 mL) and extracted with chloroform (100 mL×3). The organic layer was washed with saturated brine (50 mL), followed by drying over sodium sulfate anhydrate and concentrating under reduced pressure. The residue was purified through silica gel column chromatography (eluent: chloroform:saturated ammonia in methanol=20:1). The thus-obtained oily product was crystallized from ethanol-diethyl ether, thereby yielding 1.16 g of 2-[4-[2-(benzimidazol-2-ylthio)ethyl]piperazin-1-yl]-N-[2,4-bis(methylthio)-6-methylpyridin-3-yl]acetamide (yield: 88%) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06998486B2
Source datasetuspto-grants-2006_02
ORD IDord-58e4656eb8a74f49a9ebbc61794f2920
Source noteuspto-grants-2006_02