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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573264Generated: October 29, 2026

Methyl iodide → 3-bromo-1-methyl-1H-Pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/573264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromo-1H-pyrrolo[3,2-b]pyridineHCID 44119213—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-bromo-1-methyl-1H-Pyrrolo[3,2-b]pyridineHCID 6672789584.7%

Reaction Steps

A mixture of 3-bromo-1H-pyrrolo[3,2-b]pyridine (450 mg) in DMF (5 mL) was treated with a NaH (60% in oil, 100 mg) and the resulting mixture stirred at room temperature for 5 min. The mixture was cooled to 0° C., treated with MeI (324 mg) then allowed to warm to room temperature over a period of 1 h. After this time, the reaction was diluted with water (100 mL) and extracted with AcOEt (3×50 mL). The combined organics were washed with water (50 mL), 5% LiCl aqueous solution (50 mL) then brine (50 mL), dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (heptane to AcOEt) to give the title compound (408 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029536B2
Source datasetuspto-grants-2015_05
ORD IDord-0ccae535d7694ee7a343d1fc214fdd8d
Source noteuspto-grants-2015_05