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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633515Generated: October 26, 2026

Methyl iodide → 3-iodo-7-methoxy-1-methyl-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/633515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 53412719—
SolventDimethylformamideHCID 6228—
Product3-iodo-7-methoxy-1-methyl-1H-pyrrolo[2,3-c]pyridineHCID 9038781395%

Reaction Steps

3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine (0.75 g, 2.74 mmol) in dimethylformamide (10 mL) was treated with 60% sodium hydride in mineral oil (0.219 g, 5.47 mmol) at room temperature for 20 minutes. To this solution was added methyl iodide (0.505 g, 3.56 mmol). The reaction mixture was stirred for 3 hours at room temperature. The reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 10% ethyl acetate/hexanes to give 0.75 g (95%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321764B2
Source datasetuspto-grants-2016_04
ORD IDord-1dd57418a9094f3e8ee3a63fc3515d58
Source noteuspto-grants-2016_04