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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573365Generated: October 30, 2026

Water → (1-(2,2-Difluoroethyl)-6-fluoro-1H-pyrazolo[4,3-b]pyridin-3-yl]phenol

https://huagongshe.com/reaction/573365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant2,2-Difluoroethyl trifluoromethanesulfonateHCID 2774089—
Reactant3-[4-(Benzyloxy)phenyl]-6-fluoro-1H-pyrazolo[4,3-b]pyridineHCID 66728048—
SolventDimethylformamideHCID 6228—
Product(1-(2,2-Difluoroethyl)-6-fluoro-1H-pyrazolo[4,3-b]pyridin-3-yl]phenolHCID 136409095—

Reaction Steps

To a stirred mixture of 3-[4-(benzyloxy)phenyl]-6-fluoro-1H-pyrazolo[4,3-b]pyridine (100 mg) and Cs2CO3 (204 mg) in DMF (4 mL) was added 2,2-difluoroethyl trifluoromethanesulfonate (73.8 mg) at 0° C. The mixture was stirred at room temperature for 12 h, treated with water, and extracted with AcOEt. The organic layer was dried over MgSO4 and concentrated under reduced pressure. The residue was dissolved in EtOH (8 mL) and 10% Pd—C (50% wet, 100 mg) was added. The mixture was stirred at room temperature for 1 h under H2 atmosphere, filtered and evaporated. The residue was purified by silica gel column chromatography (AcOEt/hexane) to give the title compound (47.0 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029536B2
Source datasetuspto-grants-2015_05
ORD IDord-a9c796384a4b4c2194603e10da6e9270
Source noteuspto-grants-2015_05