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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766704Generated: November 3, 2026

Cesium carbonate → 3-(3-Methoxy-benzyloxy)-5-phenyl-pyridin-2-ylamine

https://huagongshe.com/reaction/1766704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-Methoxybenzyl bromideHCID 4067207—
Reactant5-Phenyl-2-(trityl-amino)-pyridin-3-olHCID 21111499—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product3-(3-Methoxy-benzyloxy)-5-phenyl-pyridin-2-ylamineHCID 1042526160%

Reaction Steps

To a solution of 5-phenyl-2-(trityl-amino)-pyridin-3-ol (100 mg, 0.24 mmol) in THF (3 mL) was added Cs2CO3 (79 mg, 0.24 mmol). The mixture was stirred at room temperature for 20 minutes, and then 3-methoxybenzylbromide (0.037 mL, 0.26 mmol) was added. The reaction was stirred at room temperature overnight, diluted with dichloromethane (5 mL), and filtered to remove the salts. The solvents were evaporated, and the residue was dissolved in 10% trifluoroacetic acid in dichloromethane (2 mL). The reaction was stirred for 2 hr, and evaporated. The residue was dissolved in dichloromethane, washed by sat. NaHCO3, and dried over Na2SO4. After filtration and concentration, the crude product was purified on a silica gel column eluting with methanol-dichloromethane (from 3% to 15% gradient) to provide 3-(3-methoxy-benzyloxy)-5-phenyl-pyridin-2-ylamine as a white solid (43.5 mg, 60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230098B2
Source datasetuspto-grants-2007_06
ORD IDord-67e78069dde74b8dbb3a30ab06f60c31
Source noteuspto-grants-2007_06