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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2070026Generated: November 1, 2026

4-[1-(4-Methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yloxy]aniline → 4-(1H-pyrazolo[3,4-b]pyridin-4-yloxy)aniline

https://huagongshe.com/reaction/2070026

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[1-(4-Methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yloxy]anilineHCID 59398527—
SolventTrifluoroacetic acidHCID 6422—
Product4-(1H-pyrazolo[3,4-b]pyridin-4-yloxy)anilineHCID 5939854288%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-[1-(4-Methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-yloxy]aniline (263 mg) was dissolved in TFA (7.5 mL). The resulting mixture was stirred at 60° C. for 2 hours and concentrated under reduced pressure. The residue was diluted with dichloromethane and then washed with a sodium bicarbonate solution and saturated brine. The organic layer was separated and concentrated under reduced pressure. The residue was suspended in ether, and the precipitate was collected by filtration to give 4-(1H-pyrazolo[3,4-b]pyridin-4-yloxy)aniline (151 mg, yield: 88%) as a light-brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299252B2
Source datasetuspto-grants-2012_10
ORD IDord-83cd822d725c415caa649f5eb6e79c20
Source noteuspto-grants-2012_10