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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2273233Generated: October 30, 2026

Sodium Hydroxide → 4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/2273233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 4-chloro-6-methoxy-1,5-naphthyridine-3-carboxylateHCID 23209173—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acidHCID 6725557296.1%

Reaction Steps

Sodium hydroxide (5.86 g, 140.6 mmol, 2.5 eq) is added protionwise at room temperature to a stirred solution of 4-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester (15.0 g, 56.25 mmol, 1.0 eq) in tetrahydrofuran (150 mL) and water (80 mL). After 15 hours stirring at room temperature, tetrahydrofuran is removed, the aqueous layer is cooled down to 0° C. and the pH is adjusted to 3 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-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid as a light red solid (12.9 g, 96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120822B2
Source datasetuspto-grants-2015_09
ORD IDord-90cafb800b0849d6ac2a70e491527973
Source noteuspto-grants-2015_09