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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872025Generated: October 31, 2026

Potassium Iodide → 1H-Pyrrolo[2,3-b]pyridine, 4-fluoro-1-(3-methoxypropyl)-

https://huagongshe.com/reaction/872025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium hydrideHCID 24758—
Reactant1-Bromo-3-methoxypropaneHCID 524551—
Reactant4-Fluoro-1H-pyrrolo(2,3-b)pyridineHCID 11297998—
SolventDimethylformamideHCID 6228—
Product1H-Pyrrolo[2,3-b]pyridine, 4-fluoro-1-(3-methoxypropyl)-HCID 5949422388.5%

Reaction Steps

60% Oily sodium hydride (135 mg) was added to a solution of 4-fluoro-1H-pyrrolo[2,3-b]pyridine (384 mg) in N,N-dimethylformamide (6 ml) and the mixture was stirred at room temperature for 1.5 hours. 1-Bromo-3-methoxypropane (518 mg) and potassium iodide (468 mg) were added to the mixture and the reaction mixture was stirred at 50° C. for 1.5 hours. Ice water was added to the reaction mixture slowly and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine successively, dried over magnesium sulfate and concentrated in vacuo. The resulted residue was purified with a silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=90/10 to 70/30) to give 4-fluoro-1-(3-methoxypropyl)-1H-pyrrolo[2,3-b]pyridine (520 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975252B2
Source datasetuspto-grants-2015_03
ORD IDord-b911b8d18efd4b2c833c1a959c427d9c
Source noteuspto-grants-2015_03