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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050257Generated: November 2, 2026

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

https://huagongshe.com/reaction/1050257

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. 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 numberUS09382243B2
Source datasetuspto-grants-2016_07
ORD IDord-1d72bb6ca1494533aaab85e64b3a94ff
Source noteuspto-grants-2016_07