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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659953Generated: October 30, 2026

2-Fluoroethyl bromide → HCID 86643499, compound

https://huagongshe.com/reaction/659953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoroethyl bromideHCID 12982—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 10871025HCID 10871025—
SolventDimethylformamideHCID 6228—
ProductHCID 86643499HCID 8664349962.8%

Reaction Steps

Sodium hydride (371 mg, 9.3 mmoles 60% in oil) is added to a solution of 1 g (3.1 mmoles) of 2-(2-Chloro-pyridin-4-yl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridine (prepared following the procedure for example 6) in 20 mL of dimethylformamide at room temperature. After 30 min. at room temperature, 2.75 g of 1-bromo-2-fluoro-ethane (21.6 mmoles) is added to the reaction mixture. After 10 hour at room temperature, the reaction mixture is poured into ammonium chloride solution and extracted with ethyl acetate. The organic phase is washed with water and dried over magnesium sulfate. After concentration the solid residue is purified by chromatography on silica gel (ethyl acetate/hexane 1/1) to give 720 mg of 2-(2-Chloro-pyridin-4-yl)-1-(2-fluoro-ethyl)-3-(4-fluoro-phenyl)-1H-pyrrolo[3,2-b]pyridine as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084395B2
Source datasetuspto-grants-2011_12
ORD IDord-a2249097ab654673a35db6e03cb522c7
Source noteuspto-grants-2011_12