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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2208992Generated: October 30, 2026

Sodium Thiosulfate → 6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/2208992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant6-chloro-3-methyl-4-(methylthio)-3H-imidazo[4,5-c]pyridineHCID 117843414—
SolventDichloromethaneHCID 6344—
Product6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridineHCID 117842888—

Reaction Steps

To a solution of 6-chloro-3-methyl-4-(methylthio)-3H-imidazo[4,5-c]pyridine 2.02 (450 mg, 2.11 mmol) in dichloromethane (16 mL) at 0° C., was added mCPBA (≦77%, 972 mg, 4.34 mmol) and mixture was warmed to room temperature. After 80 minutes, an additional 200 mg of mCPBA was added. After an additional twenty minutes, a solution of 50% saturated Na2S2O3 (aq) (20 mL) was added and reaction mixture stirred at room temperature for fifteen minutes. Layers were separated and aqueous was extracted with ethyl acetate (4×15 mL). All organic layers were combined, washed with saturated NaHCO3 (aq) (2×30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to yield 6-chloro-3-methyl-4-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine 2.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-805407c88c194a49bb78907c01418752
Source noteuspto-grants-2016_06