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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050256Generated: November 1, 2026

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

https://huagongshe.com/reaction/1050256

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 C7H5ClIN3S 325.56, observed m/e: 325.88 (M+H)+ (Rt 2.05/5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382243B2
Source datasetuspto-grants-2016_07
ORD IDord-f005345b921f448baad35dfa87d24d9f
Source noteuspto-grants-2016_07