Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266261Generated: October 30, 2026

Chloroacetyl chloride → N-[5-(3-Bromo-phenylamino)-6-cyano-[1,8]naphthyridin-3-yl]-2-chloro-acetamide

https://huagongshe.com/reaction/1266261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Amino-4-(3-bromo-phenylamino)-[1,8]naphthyridine-3-carbonitrileHCID 9949813—
SolventTetrahydrofuranHCID 8028—
ProductN-[5-(3-Bromo-phenylamino)-6-cyano-[1,8]naphthyridin-3-yl]-2-chloro-acetamideHCID 1854898876.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 0.74 g (2.2 mmol) of 6-amino-4-(3-bromo-phenylamino)-[1.8]naphthyridine-3-carbonitrile and 0.7 g (5.44 mmol) of disopropylethyl amine in a 7 ml of N-methylpyrrolidone was added with stirring at 0° C. a solution of 0.29 g (2.6 mmol) of chloroacetyl chloride in 5 ml of tetrahydrofuran over 5 min. After 1 hr at 0° C. the mixture was warmed to room temperature. The mixture was poured into saturated sodium bicarbonate. Solid was collected and air dried. The solid was purified by chromatography on silica gel eluting with ethyl acetate-methanol mixtures giving 0.7 g of the title compound as a tan solid: mass spectrum (electrospray, m/e): M+H 416.1, 418.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548496B2
Source datasetuspto-grants-2003_04
ORD IDord-b435168a6c6244229330ef1ba385db53
Source noteuspto-grants-2003_04