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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851094Generated: November 2, 2026

Hydrochloric Acid → 3-fluoro-4-(2-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yloxy)-phenylamine

https://huagongshe.com/reaction/1851094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-fluoro-4-[2-phenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-4-yloxy]-phenyl-carbamic acid t-butyl esterHCID 58368390—
SolventMethanolHCID 887—
Product3-fluoro-4-(2-phenyl-1H-pyrrolo[2,3-b]pyridin-4-yloxy)-phenylamineHCID 5836835940%

Reaction Steps

To a solution of 3-fluoro-4-[2-phenyl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrrolo[2,3-b]pyridin-4-yloxy]-phenyl-carbamic acid t-butyl ester in methanol, a 1:1 solution (10 mL) of hydrochloric acid and methanol was added. The mixture was stirred at room temperature for 4 hours. The resulting reaction mixture was concentrated under reduced pressure and ether was added to the resulting residue. After stirring for 2 hours, the produced solid was collected by filtering. Thus obtained hydrochloride was dissolved in water and neutralized to about pH 8 by adding 1 M sodium hydroxide aqueous solution. The resulting mixture was extracted with ethyl acetate. The organic layer was separated and washed with sodium chloride aqueous solution. The organic layer was dried with Na2SO4 and then filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexane:ethyl acetate=1:1) to give the target compound as a white solid (81 mg, 0.25 mmol, 40% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957102B2
Source datasetuspto-grants-2015_02
ORD IDord-e5dbc61b7312445b85c8a27c4bc90c77
Source noteuspto-grants-2015_02