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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422946Generated: October 31, 2026

Benzyl Alcohol → 4-Benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/1422946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
Reactant4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acidHCID 67255572—
SolventDimethylformamideHCID 6228—
Product4-Benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acidHCID 6725502798%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Benzyl alcohol (5.78 g, 53.43 mmol, 2.5 eq) is added at −45° C. to a stirred solution of 4-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid (5.1 g, 21.37 mmol, 1.0 eq) in N,N-dimethylformamide (100 mL), followed by sodium hydride (2.46 g, 53.43 mmol, 2.5 eq). After 2 hours stirring at −40° C. and 24 hours stirring at room temperature, the reaction mixture is quenched with ice water, the pH is adjusted to 3-4 by the addition of a 2N hydrochloric acid aqueous solution. The resulting precipitate is collected by filtration, washed with water and dried under high vacuum to afford 4-benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acid as a light red solid (6.5 g, 98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-e6db21d475a842b49712caf53e0575aa
Source noteuspto-grants-2015_01