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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727362Generated: November 1, 2026

Potassium Persulfate → 4-(3-METHYLPHENYL)-5-(2-METHYL-4-PYRIDYL)-2-(4-METHYLSULFINYLPHENYL)-1,3-THIAZOLE

https://huagongshe.com/reaction/1727362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium PersulfateHCID 24412—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(3-METHYLPHENYL)-5-(2-METHYL-4-PYRIDYL)-2-[4-(METHYLTHIO)PHENYL]-1,3-THIAZOLEHCID 10134891—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-(3-METHYLPHENYL)-5-(2-METHYL-4-PYRIDYL)-2-(4-METHYLSULFINYLPHENYL)-1,3-THIAZOLEHCID 1022291126.5%

Reaction Steps

To a solution of 4-(3-methylphenyl)-5-(2-methyl-4-pyridyl)-2-[4-(methylthio)phenyl]-1,3-thiazole (0.55 g, 1.4 mmol) in acetic acid (15 mL) was added a solution of potassium persulfate (0.43 g, 1.6 mmol) in water (8 mL), and the mixture was stirred for 14 hours at room temperature. An aqueous sodium hydrogen carbonate solution was poured into the reaction mixture, and extracted with ethyl acetate. The extracts were washed with water, dried, then, the solvent was distilled off. The residue was purified by column chromatography (filler: Chromatorex NH DM1020 (trade name, manufactured by Fuji Silysia Chemical Ltd.), hexane-ethyl acetate=1:4), and recrystallized from ethyl acetate-hexane to obtain a title compound (0.15 g, yield 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495018B2
Source datasetuspto-grants-2009_02
ORD IDord-d842e8909a8641f28a3b4a40a337a983
Source noteuspto-grants-2009_02