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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478543Generated: October 27, 2026

Potassium bis(trimethylsilyl)amide → 6-Bromo-4-hydroxy-1,5-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/1478543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantEthyl 3-acetamido-6-bromopyridine-2-carboxylateHCID 90044467—
SolventTetrahydrofuranHCID 8028—
Product6-Bromo-4-hydroxy-1,5-naphthyridin-2(1H)-oneHCID 90042975—

Reaction Steps

To a solution of KHMDS (0.5 M in toluene, 27 ml, 14 mmol) at −78° C. was slowly added a solution of ethyl 3-acetamido-6-bromo-pyridine-2-carboxylate (1.3 g, 4.5 mmol) in THF (20 ml). Stirring was continued for 1 h at this temperature then the cooling bath was removed. Ethyl acetate followed by water was added at ambient temperature, then the phases were separated. The yellow aqueous phase was treated with HCl (1 M) until a colorless solid was formed. Filtration and washing of the solid with water followed by drying afforded 6-bromo-4-hydroxy-1H-1,5-naphthyridin-2-one as a colorless solid. The compound is exclusively present in the tautomer shown.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403845B2
Source datasetuspto-grants-2016_08
ORD IDord-d453ee0bbda44dab920dc6c73f81c1dc
Source noteuspto-grants-2016_08