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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503652Generated: October 26, 2026

Dimethylformamide → 3-(Benzyloxy)-8-chloro-1,5-naphthyridine

https://huagongshe.com/reaction/503652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant8-Chloro-1,5-naphthyridin-3-olHCID 135743576—
SolventDichloromethaneHCID 6344—
Product3-(Benzyloxy)-8-chloro-1,5-naphthyridineHCID 67316944—

Reaction Conditions

Temperature65 °C

Reaction Steps

A pyrex reaction tube was charged with 8-chloro-1,5-naphthyridin-3-ol (165 mg, 914 μmol), potassium carbonate (631 mg, 4568 μmol), 1-(chloromethyl)benzene (376 μl, 4568 μmol) and 3.7 mL DMF. The tube was sealed and the mixture was heated at 65° C. for 3 h. The reaction was diluted with DCM and washed with water. The organic portion was dried, filtered, and concentrated. The crude material was purified by silica gel chromatography, 0-25% EtOAc in DCM to provide product as a white solid. MS: [M+H]=271.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-26b80b1805dc49fba2d7868dc93ec818
Source noteuspto-grants-2010_08