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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256184Generated: November 1, 2026

Ammonia → 7-Bromo-1,5-naphthyridin-2-amine

https://huagongshe.com/reaction/1256184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantWaterHCID 962—
Reactant7-Bromo-2-chloro-1,5-naphthyridineHCID 58310544—
Solvent1,4-DioxaneHCID 31275—
Product7-Bromo-1,5-naphthyridin-2-amineHCID 5831053280%

Reaction Conditions

Temperature160 °C

Reaction Steps

In a sealed reactor, 500 mg (1.23 mmol, 1 eq) of 7-bromo-2-chloro-1,5-naphthyridine and 7 mL (41.6 mmol, 33 eq) of 20% aqueous ammonia solution were introduced in 7 mL of dioxane. The mixture was stirred at 160° C. for 24 h. The mixture was allowed to reach rt and water was added. Aqueous layer was extracted with ethyl acetate. Organic layers were dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography using methylene chloride and then methylene chloride/ethanol: 98/2 as eluent. The solvent was evaporated to dryness to afford 220 mg of white powder with 80% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461178B2
Source datasetuspto-grants-2013_06
ORD IDord-6b8b6c9b669a4c45981c5dbd5658792a
Source noteuspto-grants-2013_06