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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82464Generated: October 30, 2026

Methyl iodide → 1-methyl-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde

https://huagongshe.com/reaction/82464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant1H-Pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 21963887—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-methyl-1H-pyrrolo[2,3-b]pyridine-4-carbaldehydeHCID 57742985—

Reaction Steps

To a solution of 1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde (0.252 g, 1.72 mmol) in 1 mL of DMF under an atmosphere of nitrogen was added sodium hydride (45.5 mg, 1.90 mmol). After 5 min, iodomethane (0.13 mL, 2.1 mmol) was added. After 30 min, the reaction was treated with saturated aqueous ammonium chloride, diluted with water, and extracted 2× with dichloromethane. The combined organic solution was washed 3× with water, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-40% ethyl acetate in hexanes to provide 1-methyl-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde that gave proton NMR spectra consistent with theory and a mass ion (ES+) of 161.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846702B2
Source datasetuspto-grants-2014_09
ORD IDord-714f7db371f14597954bde496083ef87
Source noteuspto-grants-2014_09