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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929172Generated: October 31, 2026

Methyl iodide → 6-Chloro-5-iodo-2-(methylthio)-1H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/929172

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant6-Chloro-5-iodo-1H-imidazo[4,5-b]pyridine-2(3H)-thioneHCID 86684739—
SolventEthanolHCID 702—
Product6-Chloro-5-iodo-2-(methylthio)-1H-imidazo[4,5-b]pyridineHCID 89558265—

Reaction Steps

A suspension of 6-chloro-5-iodo-1,3-dihydro-2H-imidazo[4,5-b]pyridine-2-thione (11.0 g, 35.3 mmol) and KOH (2.38 g, 42.4 mmol) in ethanol (200 mL) was stirred at rt for 0.5 h. Iodomethane (2.2 mL, 35.3 mmol) was then added and the reaction was allowed to stir for 1 h at rt. The ethanol was removed in vacuo and the resulting residue was partitioned between ethyl acetate (250 mL) and 2N HCl (50 mL). The ethyl acetate layer was washed with brine, dried over magnesium sulfate, filtered through a 100 g pad of silica gel and concentrated to give the desired product as a white solid. LC-MS: calculated for C2H5ClIN3S 325.56, observed m/e: 325.88 (M+H)+ (Rt 2.05/5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-192b975a4b594e2dbe985661853cbf75
Source noteuspto-grants-2016_03