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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75272Generated: October 29, 2026

Methyl iodide → 6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridine

https://huagongshe.com/reaction/75272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1H-pyrrolo[3,2-b]pyridineHCID 24229256—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Bromo-1-methyl-1H-pyrrolo[3,2-b]pyridineHCID 6738310293%

Reaction Steps

Sodium hydride (60%, 670 mg, 16.8 mmol) was added to a solution of 6-bromo-1H-pyrrolo[3,2-b]pyridine (3.00 g, 15.2 mmol) in DMF (20 mL) at 0° C., and the reaction mixture was stirred for 30 minutes. Iodomethane (1.05 mL, 16.8 mmol) was added. The reaction mixture was subsequently stirred for 30 minutes while warming to RT, diluted with EtOAc, quenched and washed with brine. The aqueous layer was extracted with EtOAc (2×) and the combined organic layers were dried over MgSO4, concentrated, and purified by silica gel chromatography (50% EtOAc/DCM) to give the title compound as a white solid (2.98 g, 93%). 1H NMR (500 MHz, DMSO-d6) δ ppm 8.38 (d, 1H, J=2.0 Hz), 8.21 (d, 1H, J=2.0 Hz), 7.65 (d, 1H, J=3.5 Hz), 6.57 (d, 1H, J=3.5 Hz), 3.81 (s, 3H); ESI-MS m/z [M+H]+ calc'd for C8H7BrN2, 211, 213; found 211, 213.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835420B2
Source datasetuspto-grants-2014_09
ORD IDord-7b662015993e4db0b119213dd6a5835a
Source noteuspto-grants-2014_09