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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497373Generated: October 27, 2026

Triphenylphosphine → 4-[(3-chlorobenzyl)oxy]-1-(2,3-dimethyl-2H-indazol-5-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1497373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-Chlorobenzyl alcoholHCID 70117—
Reactant1-(2,3-dimethyl-2H-indazol-5-yl)-4-hydroxypyridin-2(1H)-oneHCID 117798670—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-[(3-chlorobenzyl)oxy]-1-(2,3-dimethyl-2H-indazol-5-yl)pyridin-2(1H)-oneHCID 11779866348.4%

Reaction Steps

To a suspension of 1-(2,3-dimethyl-2H-indazol-5-yl)-4-hydroxypyridin-2(1H)-one (50 mg), (3-chlorophenyl)methanol (56 mg) and triphenylphosphine (154 mg) in tetrahydrofuran (5 ml) was added bis(2-methoxyethyl)azodicarboxylate (138 mg) at room temperature, and the mixture was stirred at the same temperature for 3 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol) to give the title compound (36 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199963B2
Source datasetuspto-grants-2015_12
ORD IDord-401684d8cc1046f98b2c266e63cb66dc
Source noteuspto-grants-2015_12