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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75035Generated: October 30, 2026

Bromine → 5-fluoro-4-methoxy-3-bromo-1-tosyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/75035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant5-fluoro-4-methoxy-1-tosyl-1H-pyrrolo[2,3-b]pyridineHCID 68007883—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product5-fluoro-4-methoxy-3-bromo-1-tosyl-1H-pyrrolo[2,3-b]pyridineHCID 68007702—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cold (0° C.) solution of 5-fluoro-4-methoxy-1-tosyl-1H-pyrrolo[2,3-b]pyridine, 68b, (0.79 g, 2.45 mmol) in chloroform (50 mL) was added bromine (0.13 mL, 2.45 mmol). The reaction mixture was stirred at 0° C. for 3 hours and then slowly warmed to ambient temperature. The mixture was diluted with deionized water and quenched with aqueous sodium bicarbonate. The aqueous phase was extracted with methylene chloride and dried over sodium sulfate. The resulting solid was purified via silica gel chromatography (15-30% EtOAc/Hexanes) to give 170 mg of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829007B2
Source datasetuspto-grants-2014_09
ORD IDord-d114db063dde45f7909760aa2c12cdae
Source noteuspto-grants-2014_09