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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051487Generated: October 31, 2026

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

https://huagongshe.com/reaction/1051487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-7-azaindoleHCID 11159915—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-methyl-1H-pyrrolo[2,3-b]pyridineHCID 8672926837.2%

Reaction Steps

To a solution of 6-bromo-1H-pyrrolo[2,3-b]pyridine (500 mg, 2.55 mmol) in DMF (10 mL) was added NaH (306 mg, 7.65 mmol, m %/60%). The mixture was stirred at room temperature for 1 h and then MeI (398 mg, 2.8 mmol) was added. The reaction mixture was then stirred at room temperature for 4 h after which, TLC showed the completion of the reaction. The reaction mixture was quenched by addition of water and then extracted with EtOAc. Combined organic layers were concentrated and the residue was purified by Prep-TLC (PE:EA=5:1) to give the desired product (200 mg) which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388173B2
Source datasetuspto-grants-2016_07
ORD IDord-7e45ef7bef5a4b1b9ef255b972a15f03
Source noteuspto-grants-2016_07