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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 551493Generated: November 1, 2026

Ethyl Acetate → 4-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-1-(tetrahydro-pyran-2-yl)-1H-indazole

https://huagongshe.com/reaction/551493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromomethyl-1-(tetrahydro-pyran-2-yl)-1H-indazoleHCID 22661215—
Reactant4',5'-Difluoro-2'-methoxy-biphenyl-4-olHCID 58259993—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(4',5'-difluoro-2'-methoxy-biphenyl-4-yloxymethyl)-1-(tetrahydro-pyran-2-yl)-1H-indazoleHCID 6715193452.5%

Reaction Steps

4-Bromomethyl-1-(tetrahydro-pyran-2-yl)-1H-indazole (0.5 g, 1.69 mmol), 3-(4′,5′-difluoro-2′-methoxy-biphenyl-4-ol (0.4 g, 1.69 mmol) and potassium carbonate (0.23 g, 1.69 mmol) in 15 mL THF/3 mL DMF was heated to 70° C. overnight. The reaction was cooled and distributed between EtOAc and H2O. The organic layer was separated and concentrated in vacuo. The crude product was purified by flash chromatography with a gradient from 0-25% ethyl acetate in hexanes to yield 4-(4′,5′-difluoro-2′-methoxy-biphenyl-4-yloxymethyl)-1-(tetrahydro-pyran-2-yl)-1H-indazole as a white solid (400 mg, 52.5%). HR-MS (ES) calculated for C26H24F2N2O3, 473.1646; found m/z 473.1647 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947728B1
Source datasetuspto-grants-2011_05
ORD IDord-e6a3e5888284475b8b47c946844e1988
Source noteuspto-grants-2011_05