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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401144Generated: November 1, 2026

Acetonitrile → 6-Chloro-5-iodo-2-(methylsulfonyl)-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/2401144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium hydroxy sulfiteHCID 23707502—
Reactant6-Chloro-5-iodo-2-(methylthio)-1H-imidazo[4,5-b]pyridineHCID 89558265—
SolventWaterHCID 962—
Product6-Chloro-5-iodo-2-(methylsulfonyl)-3H-imidazo[4,5-b]pyridineHCID 89558234—

Reaction Steps

Oxone (20.8 g, 33.8 mmol) was added to an acetonitrile (100 mL)/water (100 mL) suspension of 6-chloro-5-iodo-2-(methysulfanyl)-1H-imidazo[4,5-b]pyridine (5.0 g, 15.4 mmol) and the reaction was allowed to stir for 18 h at rt. The suspension was filtered through a sintered glass funnel and the filtrate was partitioned between ethyl acetate and saturated sodium bisulfate. The ethyl acetate layer was washed with brine, dried over magnesium sulfate and concentrated to afford the title compound as a white solid that was used in subsequent steps without further purification. Solubility precludes purification and this was used as is. LC-MS: calculated for C7H5ClN3O2S 357.56, observed m/e: 357.07 (M+H)+ (Rt 1.36/4 min) 1H NMR δ (ppm) (DMSO-d6): 8.44 (1H, s), 3.53 (3H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796258B2
Source datasetuspto-grants-2014_08
ORD IDord-98816a628638423f9ba5d36e2460d603
Source noteuspto-grants-2014_08